ITEM
1. BUSINESS
Overview
We
are a clinical-stage biotechnology company dedicated to enabling cures through hematopoietic stem cell therapy. We are focused on the
development and commercialization of safer and more effective conditioning agents and stem cell engineering to allow for expanded use
of stem cell transplantation and ex vivo gene therapy, a technique in which genetic manipulation of cells is performed outside of the
body prior to transplantation.
Our
drug development pipeline includes multiple product candidates designed to improve hematopoietic stem cell therapy. Our lead product
candidate, JSP191, is in clinical development as a novel conditioning antibody that clears hematopoietic stem cells from bone marrow
in patients prior to undergoing allogeneic stem cell therapy or stem cell gene therapy. We are also developing engineered hematopoietic
stem cells (“eHSC”) product candidates reprogrammed using mRNA delivery and gene editing that have a competitive advantage
over endogenous hematopoietic stem cells (“HSCs”) because they permit higher levels of engraftment without the need for toxic
conditioning of the patient and with potentially lower risk of other serious complications seen with current stem cell transplants. We
also plan to continue to expand our pipeline to include other novel stem cell therapies based on immune modulation, graft engineering
or cell and gene therapies. Our goal is to expand the use of curative stem cell transplant and gene therapies for all patients, including
children and the elderly.
Stem cell transplantation is among the most widely
practiced forms of cellular therapy and has the potential to cure a wide variety of diseases, including cancers, genetic disorders and
autoimmune diseases. A stem cell transplant procedure involves three main steps: (i) stem cells from the patient’s or donor’s
bone marrow are collected; (ii) the patient’s bone marrow is cleared of any remaining stem cells in order to make space to receive
new transplanted stem cells, which is known as conditioning; and (iii) the new stem cells are transplanted into the patient via infusion
where they fasten to, or engraft in, the bone marrow and grow into the blood and immune cells that form the basis of reset and rebuilt
blood and immune systems. Transplants are either allogeneic or autologous, depending on the source of the new stem cells for the transplant.
In an allogeneic transplant, patients receive cells from a stem cell donor. In an autologous transplant, the patient’s own stem
cells are used. Autologous transplants also include stem cell gene therapies, where cells are collected from the patient, edited to either
enable a functioning gene or correct a defective gene, and then transplanted into the patient via infusion. Our programs span both allogeneic
and gene therapy-based autologous transplants, with initial sponsored programs in JSP191 based on an allogeneic approach.
Currently,
patients must receive highly toxic and potentially life-threatening conditioning agents to prepare their bone marrow for transplantation
with either donor stem cells or their own gene-edited stem cells. Younger, fitter patients capable of surviving these toxic side effects
are typically given myeloablative, or high-intensity, conditioning whereas older or less fit patients are typically given reduced intensity,
but still toxic, conditioning which leads to less effective transplants. These toxicities include a range of acute and chronic effects
to the gastrointestinal tract, kidneys, liver, lung, endocrine, and neurologic tissues. Depending upon the conditioning regimen, fitness
of the patient, and compatibility between the donor and recipient, the risk of transplant-related mortality ranges from 10% to more than
50% in older patients. Less toxic ways to condition patients have been developed to enable transplant for older patients or those with
major comorbidities, but these regimens risk less potent disease elimination and higher rates of disease relapse. Even though stem cell
therapy can be one of the most powerful forms of disease cure, these limitations of non-targeted conditioning regimens have seen little
innovation over the past decade.
![](https://content.edgar-online.com/edgar_conv_img/2022/03/18/0001213900-22-013592_image_001.jpg)
Our lead product candidate, JSP191, is a monoclonal antibody designed
to block a specific survival signal on stem cells and is in development as a highly targeted conditioning agent prior to stem cell therapy.
We are developing JSP191 for severe combined immunodeficiency (“SCID”) for which we are currently conducting an open label
Phase 1/2 clinical trial in two cohorts of SCID patients: patients with a history of a prior allogeneic transplant for SCID but with poor
graft outcomes and newly diagnosed SCID patients. The primary endpoint in Phase 1 is to evaluate the safety and tolerability of JSP191.
The two primary efficacy endpoints in Phase 2 are the proportion of subjects achieving adequate donor HSC engraftment and the proportion
of subjects achieving naïve T cell production greater than or equal to 85 cells/uL, a level expected to provide immune reconstitution,
during weeks 36 to 104 post-transplant. Based on preliminary results from our ongoing Phase 1/2 clinical trial, we believe JSP191 has
demonstrated the ability as a single agent to enable engraftment of donor HSCs as determined by donor chimerism, or the percentage of
bone marrow cells in the patient that are of donor origin after transplant. Six out of the first nine non-IL2RG patients with prior allogeneic
transplant achieved donor engraftment, naïve donor T cell production and demonstrated clinical improvement. No JSP191 treatment-related
serious adverse events (“SAEs”) have been reported to date and pharmacokinetics have been consistent with earlier studies
in healthy volunteers. We expect to complete enrollment in this Phase 1/2 clinical trial by mid-2023.
The
FDA has granted rare pediatric disease designation to JSP191 as a conditioning treatment for patients with SCID. In addition, the FDA
granted orphan drug designation to JSP191 for conditioning treatment prior to hematopoietic stem cell transplantation.
We also are evaluating JSP191 in an open label Phase 1 clinical trial
in patients with myelodysplastic syndrome (“MDS”) or acute myeloid leukemia (“AML”) that were transplant eligible
but still had trace evidence of leukemic cells that can remain in a patient after chemotherapy, or minimal residual disease (“MRD”),
as detected by cytogenetics, flow cytometry or next-generation sequencing. The primary endpoints are to evaluate the safety, tolerability
and pharmacokinetic parameters of JSP191. In the initial dose finding Phase 1a portion of this clinical trial, 0.6 mg/kg JSP191-based
conditioning was well tolerated in all six MDS/AML patients as of December 31, 2021. Furthermore, it led to successful engraftment as
demonstrated by sustained blood neutrophil count of >500 x 10^6 / L (Wolff 2002) in all six patients. Additionally, five of the six
patients demonstrated elimination of all diseased cells at day 90 (MRD) by multiple methods of detection, a secondary endpoint of the
clinical study. The next portion of the clinical trial, a Phase 1b dose expansion cohort has completed enrollment. Initial results from
the first seventeen patients show that 0.6 mg/kg JSP191-based conditioning was well tolerated with all seventeen patients achieving successful
engraftment. These initial results also show that twelve of fifteen Phase 1a and 1b patients with MRD at screening achieved clearance
of MRD. No JSP191-related serious adverse events have been reported. As of reporting of these initial results, four patients have come
off study, two due to relapse or disease progression, one due to late onset Grade 3 acute Graft vs Host Disease (“GvHD”) and
one due to secondary graft failure. We expect to present additional data from this study in the first half of 2022.
We have entered into a clinical collaboration with Stanford University
to study JSP191-based conditioning in patients with Fanconi anemia. This study is currently open for patient recruitment. We are also
collaborating with the National Institutes of Health to conduct clinical trials of JSP191-based conditioning in patients with sickle cell
disease (“SCD”), with chronic granulomatous disease and with GATA-2 mutated MDS. We believe that JSP191 may also be useful
for conditioning in allogenic transplant for other diseases beyond which we are currently studying, including autoimmune diseases. We
also believe that targeted JSP191-based conditioning may improve the efficacy and safety of gene therapies. We are also collaborating
with corporate partners, including Graphite Bio, Inc. (“Graphite Bio”), Aruvant Sciences GmbH (“Aruvant Sciences”)
and AVROBIO, Inc. (“Avrobio”) to study JSP191 as targeted, non-toxic conditioning for investigational gene therapies.
We plan to evaluate JSP191 as a therapeutic for
certain patients with proliferative disorders of the hematopoietic stem cell. MDS is a heterogeneous disorder of the bone marrow which
typically occurs in an older population and can progress to AML. The Revised International Prognostic Scoring System (“IPSS-R”)
is a clinical assessment tool used to evaluate risk and prognosis of newly diagnosed patients. Patients with IPSS-R scores of low or
very low are not typically referred to stem cell transplant due to the risk of transplant-related toxicities from current conditioning
regiments, infection and GvHD outweighing the patient’s expected survival with drug therapies. These patients typically suffer
from anemia, thrombocytopenia or neutropenia and are given drug therapies such as an erythropoiesis stimulating agent (“ESA”)
to stimulate production of new cells to correct their blood deficiency. However, these agents do not target the diseased hematopoietic
stem cell and patients who become refractory to ESA are dependent on routine blood transfusions, which is associated with poor survival.
ESA-refractory low-risk MDS patients have few treatment options and are a clinical unmet need.
JSP191 and other anti-CD117 monoclonal antibodies
have been shown to deplete normal and diseased MDS human hematopoietic stem cells in clinical and pre-clinical studies. In studies of
non-human primates and healthy volunteers, administration of a single dose of JSP191 resulted in depletion of healthy hematopoietic stem
cells followed by recovery in approximately six weeks. Additional recent clinical data in MDS patients undergoing stem cell transplant
showed depletion of hematopoietic stem cells after administration of JSP191 alone. By depleting diseased and healthy hematopoietic stem
cells, we believe that JSP191 may allow for preferential recovery of healthy hematopoietic stem cells and restoration of normal hematopoiesis.
We intend to study JSP191 monotherapy in low-risk MDS patients with documented cytopenia who are refractory to ESA therapy.
Our eHSC platform is designed to overcome key
limitations of stem cell transplant and stem cell gene therapy. By using mRNA delivery and/or gene editing, we believe we can reprogram
donor or gene corrected stem cells to have a transient proliferative and survival advantage over the patient’s existing cells.
We believe initial preclinical experiments by Jasper demonstrate multiple different mRNAs can be used to improve engraftment of modified
stem cells. One example are eHSCs that express certain variants of CXCR4 that may lead to improved stem cell homing and engraftment in
the bone marrow. Another example includes expression of a modified stem cell factor receptor that can lead to cell line proliferation
independent of stem cell factor (“SCF”) concentration, enabling our eHSCs to outcompete unmodified HSCs through better survival
and engraftment. Also, since JSP191 only blocks signaling through the stem cell factor receptor, these eHSCs are not affected by JSP191
when used in combination. Other initial experiments have shown that mRNA can be used to express these receptor variants on the cell surface.
We have also identified other potential receptor modifications that prevent the binding of JSP191 but retain the ability to bind SCF,
therefore allowing the eHSCs to proliferate normally even in the presence of JSP191.
We
intend to become a fully integrated discovery, development and commercial company in the field of hematopoietic stem cell therapy. We
are developing our product candidates to be used individually or, in some cases, in combination with one another. As a result, we believe
our pipeline could be tailored to the patient-specific disease so that a patient may receive more than one of our therapies as part of
his or her individual allogeneic or gene-edited stem cell therapy. Our goal is to advance our product candidates through regulatory approval
and bring them to the commercial market based on the data from our clinical trials and communications with regulatory agencies and payor
communities. We expect to continue to advance our pipeline and innovate through our research platform.
We
have an exclusive license agreement with Amgen Inc. (“Amgen”) for the development and commercialization of the JSP191 monoclonal
antibody in all indications and territories worldwide. We also have an exclusive license agreement with Stanford for the right to use
JSP191 in the clearance of stem cells prior to the transplantation of HSCs. We also entirely own the intellectual property for our eHSC
platform, which has been internally developed.
Our Product
Pipeline
We
are developing a portfolio of novel product candidates that we believe have the potential to meaningfully improve stem cell therapy for
patients with blood cancers, genetic diseases and autoimmune diseases. Additionally, we believe our product candidates have the potential
to allow more patients with debilitating or life-threatening diseases to access a one-time, transformative blood and immune reset through
transplant with better outcomes and reduced risk of toxicity and mortality versus current technologies. We are developing our product
candidates so that they can be used individually or in combination with one another, such that patients may receive more than one of
our therapies as part of their individual transplant journey. In addition to our first set of clinical product candidates, we are in
the process of identifying several other potential candidates from our engineered hematopoietic stem cell platform.
The following chart summarizes the status and
development plan for the product candidates in our pipeline. We own worldwide rights to each of our programs.
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JSP191
We
believe JSP191 is a unique, humanized, monoclonal antibody that targets the underlying biology of hematopoietic stem cells to potentially
improve the efficacy and safety of hematopoietic stem cell transplantation. JSP191 is in clinical development as a conditioning agent
to clear hematopoietic stem cells from the bone marrow prior to transplant. JSP191 binds to human CD117, a receptor for SCF, which is
expressed on the surface of hematopoietic stem and progenitor cells. The interaction of SCF and CD117 is required for stem cells to survive.
By blocking SCF from binding to CD117 and disrupting critical survival signals, JSP191 leads to the depletion of stem cells and creates
an open space in the bone marrow for donor or gene-edited stem cells to engraft. JSP191 is in clinical development both as a single conditioning
agent and in combination with existing conditioning agents depending on the need in a particular indication.
Engineered
Hematopoietic Stem Cells
Our eHSCs are designed to overcome key limitations of allogeneic donor
and autologous gene-edited stem cell transplants. By delivering mRNA or modifying DNA, leading to expression of a modified receptor or
protein, we can reprogram donor or gene-edited stem cells to have a transient proliferative and survival advantage over the patient’s
existing cells to permit higher levels of engraftment without the need for toxic conditioning of the patient. eHSCs have the potential
to eliminate the need for donor T-cells, B-cells and NK-cells which are needed in unmodified donor HSC grafts to permit robust engraftment
but can lead to GvHD, where the donor cells attack the patient’s tissues, resulting in the need for long-term immunosuppression
therapies.
Our Strategy
Our
goal is to bring curative allogeneic and autologous HSCT and gene therapy to more people by developing compounds that can make it safer
and more effective. As part of our strategy, we aim to:
Build
a leading HSCT biotechnology company to enable cures via immune modulation, graft engineering and cell and gene therapies. We
are bringing together a team of biotech veterans, leading academic institutions and a strong syndicate of healthcare-focused investors
to achieve our vision of developing an improved end-to-end stem cell transplantation process and associated therapies, starting with
safer and more effective conditioning agents and engineered stem cell therapies.
Continue to develop JSP191 as a novel, targeted
pre-transplant conditioning agent enabling more efficacious and safer HSCT. Starting with our lead product candidate, JSP191,
we are advancing the field of HSCT to address effective and safe pre-transplant conditioning in hematologic monogenic and malignant disorders
as well as in autoimmune disease and gene therapy. Our initial focus is on severe combined immunodeficiency, acute myeloid leukemia,
myelodysplastic syndrome and autologous gene-edited stem cell transplants.
Advance our eHSC platform to overcome the
limitations of current allogeneic and autologous gene-edited stem cell transplants. We are developing enhanced stem cell therapies
with transient proliferative advantages, which we believe may translate to superior efficacy and reduced GvHD compared to current standard
of care therapies in allogenic and autologous gene therapy transplants.
Commercialize
our product candidates to expand the use of effective and safe stem cell therapies for patients and physicians in our target markets.
If approved, we plan to bring our product candidates to the United States, European and Japanese markets, focusing on the top
50% of accredited transplant centers and hospital-based prescribers who administer approximately 80% of stem cell therapies. Our strong
network and relationships with key stakeholders at these centers will enable a targeted and collaborative commercial approach.
Form
and strengthen strategic collaborations with leading industry and academic organizations to further develop our pipeline, unlock the
commercial potential of our portfolio and provide enabling technologies for gene therapy collaborators. We intend to continue
collaborations with our existing partners and enter new strategic partnerships to develop additional candidates, generate evidence, and
commercialize new products in the field of stem cell therapy.
Our History
and Team
Old
Jasper was founded by Dr. Judith Shizuru, Professor of Medicine and Pediatrics at Stanford University, and Dr. Susan Prohaska, a Stanford-trained
immunologist, stem cell biologist and drug developer, with the goal of bringing curative hematopoietic stem cell transplantation to more
people by making it safer and more effective. We unite technologies from Stanford University and Amgen via expertise in stem cell transplantation,
stem cell biology and drug development. Building on bone marrow niche-clearing technology from Stanford and with our lead compound JSP191,
Dr. Shizuru initiated a clinical program funded by the California Institute for Regenerative Medicine (“CIRM”) to safely
condition patients with SCID prior to hematopoietic cell transplantation.
We
have assembled a management team of experienced biopharma industry veterans. With this leadership, we believe we are well positioned
to achieve our vision of revolutionizing hematopoietic cell transplantation with safer conditioning regimens. Ron Martell, our Chief
Executive Officer, is an experienced biopharma veteran who has extensive experience in cellular therapies and oncology drug development.
Prior to joining Jasper, Mr. Martell served as the President and CEO of MorphImmune, Inc., a private platform company advancing a highly
specific targeting technology that uses a ligand-linked payload to reprogram the immune system. Previously, he was President and CEO
of Nuvelution Pharma. He was also Co- Founder and Executive Chairman of Indapta, Orca Bio and Co-Founder and CEO of Achieve Life Sciences,
where he led the merger of the company with Oncogenex. Mr. Martell has served as the CEO of three public biopharmaceutical companies,
including Sevion and NeurogesX, and has overseen billions of dollars in industry transactions. Earlier in his career, Martell served
as Senior Vice President of Commercial Operations at ImClone Systems, where he was instrumental in deals with Bristol-Myers Squibb and
Merck KGaA and built ImClone Systems’ worldwide operations to market and commercialize Erbitux®. He also served in various leadership
positions with Genentech where, as Group Manager, Oncology, he was responsible for building the company’s oncology franchise, including
the launch of Herceptin® and Rituxan®.
Members
of our management team have held leadership positions at companies that have successfully discovered, developed, and commercialized therapies
for various cancers and devastating rare diseases. These companies include Roche, Johnson & Johnson, Genentech, Bristol-Myers Squibb,
Imclone, Incyte, Allergan, Sanofi, Amgen, Portola, Alexion and many others.
Background
on Hematopoietic Stem Cell Therapy
HSCT
is among the most widely practiced forms of cellular therapy and has the potential to cure a wide variety of diseases. Currently, its
use is limited to patients with severe disease burden due to the toxicities of current non-targeted conditioning regimens and the limitations
of the transplant grafts themselves.
Stem
cell transplants first require identification of a suitable donor and collection of the donor’s stem cells, typically from blood.
Then chemotherapy or radiation-based conditioning is used to clear the patient’s bone marrow of existing diseased stem cells in
order to make space to receive new transplanted stem cells. Finally, the donor or gene corrected stem cells are infused into the patient
where they engraft into the bone marrow and produce new blood and immune cells that form the basis of a reset and rebuilt blood and immune
system. All transplants are categorized as either autologous or allogeneic, depending on the source of the new stem cells for the transplant.
In
an autologous transplant, which is used for conditions such as multiple myeloma, non-Hodgkin’s lymphoma and certain autoimmune
diseases, the patient’s own stem cells are used. Autologous transplants also include stem cell gene therapies, in which cells are
collected from the patient, edited to either insert a functioning gene into, or correct a defective gene within, such cells and then
such cells are transplanted into the patient via infusion.
In
an allogeneic transplant, used for conditions such as acute leukemias, myelodysplastic syndromes, genetic diseases and certain autoimmune
diseases, patients receive cells from a stem cell donor. The preferred donor is a biological relative who has a well-matched immune system.
The second option is a matched unrelated donor identified through a bone marrow donor registry. Transplant outcomes are not optimal with
mismatched donors.
![](https://content.edgar-online.com/edgar_conv_img/2022/03/18/0001213900-22-013592_image_003.jpg)
Current
State of Conditioning Regimens
Currently, patients must receive highly toxic,
potentially life-threatening and non-specific conditioning agents to prepare their bone marrow for transplantation with either donor
stem cells or their own gene-edited stem cells. Current conditioning agents are genotoxic and are associated with major toxicities and
adverse events such as oral mucositis, sepsis, veno-occlusive disease, bacteremia, pulmonary fibrosis, and GvHD in the near term. In
the long term, patients must be counseled against risk of infertility of up to 70% and risk of secondary cancers of 5-10% after chemotherapy
conditioning. Additionally, there is a treatment-related mortality risk associated with current conditioning regimens that ranges from
10% to more than 50% in older patients. Other limitations of chemotherapy-based conditioning include incomplete engraftment, transplant
ineligibility and prolonged hospitalization.
Current
State of Hematopoietic Stem Cell Grafts
Hematopoietic stem cell grafts currently have limitations
around failed or poor engraftment with the risk of clinical relapse. Furthermore, GvHD is a high-risk short- and long-term adverse event
associated with HSCT as a result of donor T-cells, B-cells and NK-cells which are needed in unmodified donor HSC grafts to permit robust
engraftment. Donor immune cells may react to the patient’s tissues as foreign leading to GvHD whereas newly produced immune cells
are trained by the patient’s body to not act against the patient’s own cells. Due to this risk, patients also need to undergo
long-term immunosuppression.
Our Solution
and Product Candidates
We
are developing a conditioning agent that could significantly expand the eligible patient population for both allogeneic and autologous
gene edited hematopoietic stem cell therapies in addition to engineered hematopoietic stem cells that could result in better transplant
efficacy with reduced complications. Currently, approximately 20,000 patients receive allogeneic and autologous gene therapy transplants
each year in the major global markets (the United States, the United Kingdom, France, Germany, Spain, Italy and Japan), and we believe
this may grow to 80,000 patients with safe conditioning and more effective grafts.
JSP191
is a targeted anti-CD117 (stem cell factor receptor) antibody which we are currently evaluating in two clinical trials for conditioning
prior to stem cell transplant in patients with SCID, MDS or AML. JSP191 is designed to bind to CD117 with a greater affinity than SCF.
By blocking signaling of the stem cell factor receptor, JSP191 leads to depletion of stem cell from the bone marrow. JSP191 was also
designed to minimize any interaction with the immune system thereby reducing the risk of immune activation via mast cells or other pathways
normally activated by antibodies.
We
believe these attributes will allow JSP191 to potentially be used as a monotherapy or in combination to deplete normal and diseased stem
cells. The blocking of SCF by JSP191 may remove a critical survival signal on stem cells that leads to their depletion in the bone marrow.
Other cells (mast cells, Cajal cells, germ cells, melanocytes) that express CD117 are less dependent on SCF signaling for survival and
do not appear to be significantly affected by a single administration of JSP191. Furthermore, the mechanism of action (“MOA”)
of JSP191 on stem cells may be synergistic with other disruptors of stem cell survival such as radiation, azacytidine, and CD47. Our
MDS/AML clinical strategy aims to exploit this biology to safely clear both diseased and normal stem cells prior to transplantation of
donor cells.
The
monoclonal antibody isotype and other modifications of JSP191 were also chosen carefully to retain high affinity binding to the CD117
receptor and SCF signal blockade without recruiting other immune cells that could lead to receptor activation, mast cell degranulation
or other off-target toxicities. For example, simply changing JSP191 from an IgG1 isotype to an IgG2 isotype would result in less potent
inhibition of CD117, potentially decreasing the effect on stem cell depletion. This finding and other data demonstrate that not all anti-CD117
antibodies behave equally or have the same MOA.
Other
known approaches to target CD117, such as anti-CD117 antibodies linked to a toxin, may have off-target toxicity. In contrast to JSP191,
which provides a transient SCF signal blockade, a toxin linked anti-CD117 antibody requires internalization by CD117 expressing cells
leading to cell death. Any CD117 expressing cell including stem cells, mast cells, germ cells and melanocytes may be affected by this
mechanism. Furthermore, the complexity of an antibody-drug conjugate molecule adds to the manufacturing, clinical and regulatory risks
of the drug development process, especially for a novel linker/payload combination that may be subject to different regulatory and Chemistry,
Manufacturing and Controls (“CMC”) reviews.
![](https://content.edgar-online.com/edgar_conv_img/2022/03/18/0001213900-22-013592_image_004.jpg)
Preclinical
Data for JSP191 — General
We
conducted a preclinical study to determine if non-human primate (“NHP”) HSCs are sufficiently similar to human HSCs to allow
use of the same phenotype assays used in human studies to evaluate the effect of JSP191 on NHP hematopoiesis. This study tested, by flow
cytometry, a technique used to measure physical and chemical characteristics of a population of cells, whether homologous subsets of
NHP bone marrow express the same cellular markers as human HSCs (CD34, CD90, and CD117), and if the human antibody reagents used to identify
these markers could also be used for NHP HSCs. Bone marrow samples (or bone marrow aspirates) of NHPs and humans were stained with the
antibody reagents directed against human CD34, CD90, and CD117. HSCs in both human and NHP bone marrow were phenotypically identified
using the anti-human antibodies against CD34 and CD90. A high percentage of human and NHP cells expressing CD34 and CD90 (also CD34+
and CD90+) also express CD117. Overall, we believe these data support the use of human antibody reagents for CD34 and CD90 to assess
the effect of JSP191 on hematopoiesis in NHP in vitro and in vivo studies.
Figure
1: JSP191 binds CD117 on CD34+CD90- and CD34+CD90+ cells in human and NHP bone marrow. Left panel: flow cytometric analysis of HSCs fluorescently
labelled for CD34 and CD90. Right panel: the identified CD34+CD90- and CD34+CD90+ cells are then fluorescently labelled with 104D2 and
JSP191. JSP191 and 104D2 non-competitively labeled the same population suggesting these antibodies bind different epitopes of NHP and
human CD117.
![](https://content.edgar-online.com/edgar_conv_img/2022/03/18/0001213900-22-013592_image_005.jpg)
Non-clinical
studies in NHPs conducted at Stanford by Hye-Sook Kwon, Ph.D., now Principal Scientist at Jasper, demonstrated JSP191’s ability
to deplete bone marrow HSCs in a large animal model (Figure 2). Non-clinical studies in “humanized” mice demonstrated both
depletion of human HSCs and engraftment of allogeneic donor HSCs. These studies supported the potential for JSP191 to deplete human stem
cells prior to stem cell transplant in the IND filings for the ongoing clinical trials designed to assess the safety and efficacy of
JSP191 in HSC transplant for SCID and MDS/AML.
Figure
2: Representative flow cytometry analysis for cells fluorescently labeled with CD34 and CD90 on days 0, 10, and 42 post administration
of 1.0 mg/kg JSP191. CD34+ stem cells in the bone marrow of this NHP are transiently depleted. HSC depletion lasted up to 21 days in
most animals and more than 42 days in one NHP receiving the highest dose.
![](https://content.edgar-online.com/edgar_conv_img/2022/03/18/0001213900-22-013592_image_006.jpg)
JSP191
for Acute Myeloid Leukemia and Myelodysplastic Syndrome
AML
is a cancer of the blood and bone marrow, diagnosed in about 42,000 patients annually within the major global markets. It is primarily
a disease of the elderly and is the most common type of acute leukemia diagnosed in adults. Patients with AML are deemed eligible for
stem cell transplantation based on criteria which includes patient fitness (age and comorbidities) and response to initial treatment,
comprising of about 40% of newly diagnosed AML patients. However, stem cell transplants are administered to approximately 40% of the
eligible patient population due to current challenges with highly toxic conditioning regimens. Currently, approximately 8,000 patients
with AML receive a stem cell transplant annually in the major global markets.
MDS
is a group of disorders of the bone marrow where hematopoietic stem cells fail to properly differentiate into mature blood cells, leading
to low blood cell count. Approximately 29,000 patients are diagnosed with MDS annually in the major global markets. Of all newly diagnosed
MDS patients, about 35% have mid to high-risk disease and about 30% of those are eligible for HSCT based on age, comorbidities and blast
count. However, about 60% of MDS patients who are otherwise eligible receive a transplant due to the current challenges with highly toxic
conditioning regimens. Currently, approximately 2,500 patients with MDS receive HSCT each year.
Hematopoietic
stem cell transplantation offers the only known potentially curative therapy for many forms of AML and for MDS. Standard of care conditioning
regimens can be divided into three groups: myeloablative conditioning, reduced intensity conditioning and non-myeloablative conditioning.
Myeloablative conditioning with high dose busulfan, high dose melphalan or high dose radiation is the most aggressive approach and is
associated with the lowest rates of disease relapse. However, due to significant toxicities, including treatment related mortality, this
approach is reserved for the most fit and younger patients. Reduced intensity conditioning with lower dose busulfan or lower dose melphalan
can be used for a wider group of patients, but due to substantial toxicities, many patients remain ineligible. Non-myeloablative conditioning
with low dose radiation (200 – 450 cGy, or centigray, a unit of radiation of exposure) is well tolerated but is associated with
lower rates of successful donor chimerism and increased relapse rates compared to myeloablative or reduced-intensity conditioning.
Due
to their age and co-morbidities, older (60 years and older) and less fit MDS and AML patients are typically unable to tolerate more intensive
therapy and the toxicities associated with such treatments, and thus, have a worse prognosis than younger, fitter patients. Thus, safe
and effective conditioning prior to HSCT represents an unmet medical need for MDS and AML patients.
Preclinical
Data for JSP191 for Myelodysplastic Syndrome
Preclinical
studies of immune deficient mice engrafted with MDS HSCs from patients with “high-risk and very high-risk disease” per Revised
International Prognostic Scoring System (“R-IPSS”) criteria conducted at Stanford by Wendy Pang, M.D., Ph.D., now Vice President
of Research and Translational Medicine at Jasper, demonstrate the utility of anti-CD117 antibodies in the treatment of MDS. Mice xenografted
with high-risk MDS HSCs were treated with anti-human CD117 monoclonal antibody (“mAb”), SR-1 (the parent clone to JSP191).
Initial studies showed administration of either SR-1 or JSP191 resulted in well-tolerated and sustained depletion of MDS cells obtained
from low-risk MDS patients. Treatment of mice xenografted with high-risk MDS HSCs cells resulted in transient depletion (Figure 3). Given
the transient depletion of high-risk MDS cells, studies were conducted to determine whether an anti-CD117 antibody followed by a normal
human HSC allograft would lead to long-term disease amelioration of high-risk disease. Results showed greater than 95% cytogenetically
normal CD45+ cells 12 weeks after allograft transplant (Figure 3).
Figure
3: (A) CD117 mAb depletes MDS stem cells as demonstrated by decreasing HSC chimerism over time. (B) Normal stem cell engraftment occurs
after stem cell depletion as shown by greater than 95% cytogenetically normal CD45+ cells 12 weeks after transplant in four high-risk
MDS-xenografted mice. (C) Normal blood formation results after stem cell engraftment with human cell lineages for T cells (CD3+), B cells
(CD19+) and myeloid cells (CD13/33+) in the bone marrow of the four high-risk mice.
![](https://content.edgar-online.com/edgar_conv_img/2022/03/18/0001213900-22-013592_image_007.jpg)
Mice
xenografted with MDS HSCs from low-risk or high-risk patients were treated with SR-1 concurrently with an anti-mouse CD117 mAb, ACK2,
to suppress endogenous mouse HSCs, and then transplanted with normal human UCB. Twelve weeks after this UCB HSC transplantation, both
human myeloid and lymphoid cells like T cells and B cells were observed in the bone marrow (Figure 3), indicative of successful engraftment
and sustained hematopoiesis by healthy UCB HSCs for both risk categories. Fluorescence in situ hybridization studies assessing clonal
cytogenetic abnormalities confirmed that human CD45+ cells in both groups were predominantly (greater than 95%) cytogenetically normal
in all SR-1 treated and UCB HSC engrafted mice. In contrast, MDS xenografted mice treated with the control antibody showed a persistence
of high levels of MDS cells (greater than 95%) and were without second donor HSC engraftment.
Clinical
Data for JSP191 for Acute Myeloid Leukemia and Myelodysplastic Syndrome
We
have an ongoing open label Phase 1 clinical trial to evaluate the safety and tolerability of JSP191 conditioning, in combination with
low dose radiation (200-300 cGy) and fludarabine, in patients with AML or MDS undergoing blood stem cell transplantation. At clinical
trial entry for the dose finding portion, all patients were transplant eligible but most still had evidence of measurable residual disease
(MRD positive) as detected by cytogenetics, flow cytometry or next-generation sequencing. The starting dose of JSP191 is 0.6 mg/kg with
potential escalation up to 1.0 mg/kg, fludarabine is administered at 30 mg/m2/day on transplant days -4, -3, and -2 and total body irradiation
(“TBI”) is delivered at 200 or 300 cGy on the day of transplant. The primary endpoints are to evaluate the safety, tolerability
and pharmacokinetic parameters of JSP191. Secondary endpoints include depletion of host HSCs, donor engraftment, donor chimerism, MRD
clearance, non-relapse mortality, event-free survival and overall survival. Enrolled patients will be followed for one year. The overall
study duration is anticipated to be approximately two years.
In
the initial dose finding Phase 1a portion of this clinical trial, 0.6 mg/kg JSP191-based conditioning was well tolerated in all six MDS/AML
patients as of December 31, 2021. All six patients demonstrated evidence of successful depletion of host HSCs, observed by a reduction
of neutrophil counts (“ANC”) below 500/uL following a single infusion of JSP191 (0.6 mg/kg) in combination with 200 cGy TBI
and three days of 30 mg/m2/day fludarabine. Neutrophils are the most common type of white blood cell and are the first cells to engraft.
Following transplant, all six patients showed successful donor engraftment as evidenced by a recovery of neutrophil counts exceeding
500/uL in 19 to 26 days (Figure 4).
Figure
4: Neutrophil depletion and recovery in the first six patients of the Phase 1 MDS/AML clinical trial. All six of these initial patients
demonstrated ANC greater than 500/uL within 19 to 26 days after transplant.
![](https://content.edgar-online.com/edgar_conv_img/2022/03/18/0001213900-22-013592_image_008.jpg)
At
90 days following transplant, five of six patients demonstrated 95% or greater total donor chimerism levels as measured by CD15,
CD3 and CD56 assays. In addition, five of six patients no longer had evidence of MRD at day 90. Total donor chimerism of 95% or greater
and change in MRD status from positive to negative are both associated with reduced risk of disease relapse.
The next portion of the clinical trial,
a Phase 1b dose expansion cohort, has recently completed enrollment. Initial results from the first seventeen Phase 1a and Phase 1b patients
show that 0.6 mg/kg JSP191-based conditioning was well tolerated with all seventeen patients achieving successful engraftment. As of Day
90, each of the fourteen evaluable Phase 1a and 1b subjects achieved full myeloid donor chimerism (mean 98.4 ± 1.2%). Ten of twelve Phase 1a and 1b patients with MRD prior to transplant
no longer had evidence of MRD at Day 90. As of reporting of these initial Phase 1a and 1b results, four patients have come off study,
two due to relapse or disease progression, one due to late onset Grade 3 acute GvHD and one due to secondary graft failure (Figure 5).
Figure
5: JSP191 MDS/AML Phase 1 preliminary clinical results in the first seventeen patients. The clinical trial cohorts consisted AML/MDS
patients not eligible for standard myeloablative regimens (HCT-Cl greater than 2).
![](https://content.edgar-online.com/edgar_conv_img/2022/03/18/0001213900-22-013592_image_009.jpg)
No JSP191 related SAEs have been reported, including
no cases of oral mucositis, no cases of veno-occlusive disease. One case of grade 3 late onset GI GvHD and only two cases of chronic
GvHD of any grade have been reported, one mild and one moderate case. Since starting the study in July 2020, SAEs have been reported
in seven patients, including infections, cardiovascular events, headache, hyperkalemia and secondary graft failure, which is loss of
a previously functioning graft. None were related to treatment as determined by the investigator.
Additional data will be presented as a late-breaking
oral abstract at the 2022 Transplant and Cellular Therapy (TCT) Meetings of ASTCT and CIBMTR to be held April 23-26, 2022.
JSP191
for Severe Combined Immunodeficiency (SCID)
SCID
is a genetically heterogeneous group of over 20 monogenic conditions of the immune system characterized by the lack of normal T lymphocyte
development, in addition to deficiencies of B cells, NK cells, or both in some forms which is currently curable only by hematopoietic
cell transplant. The incidence of SCID is estimated at one in 80,000 live births across all ethnic groups. Due to the toxicities associated
with the chemotherapy regimens used in standard allogeneic hematopoietic cell transplantation (“HCT”) to deplete endogenous
HSC, some centers do not use conditioning regimens. SCID patients who undergo unconditioned HCT have relatively improved overall survival
but often experience incomplete immune reconstitution characterized by inadequate T cell numbers and/or ongoing deficiency of B cell
humoral immunity. This issue occurs more frequently in those patients who do not have a human leukocyte antigen-matched donor and who
therefore receive T cell depleted haploidentical donor grafts.
Patients
who receive full or reduced doses of busulfan tend to engraft well and have full lymphocyte reconstitution. However, due to busulfan’s
off-target toxic effects, these patients experience both short- and long-term complications. Since these patients receive busulfan (a
DNA damaging drug) as infants, they experience chronic complications such as growth retardation, cognitive defects, craniofacial abnormalities,
liver toxicity, seizure, endocrine defects including infertility and increased cancer risk.
Pre-clinical
Data for JSP191 for Severe Combined Immunodeficiency
The
ability of JSP191 to deplete human hematopoiesis was evaluated in humanized immune deficient mice that were stably engrafted with human
hematopoietic grafts at Stanford by Aaron Logan, M.D., Ph.D., et al. The mice were treated with a single dose of either 0.5 or 3.0 mg/kg
JSP191. No significant differences in depletion of human cells and HSCs after six weeks of treatment were noted between the two dose
levels of JSP191. After a single treatment with JSP191, mice were depleted of human cells in peripheral blood and bone marrow. Human
HSCs and progenitor cells (CD45+CD34+CD117+) in the bone marrow were substantially decreased for six weeks after treatment with JSP191.
To
model human transplantation with a JSP191-based conditioning regimen, humanized immune deficient mice that had been stably engrafted
with human hematopoietic cells underwent a second transplant using conditioning with JSP191 with or without the addition of an anti-CD52
antibody (Campath) that depletes human lymphocytes. The second human HSC graft was from a different donor, hence was allogeneic to the
first human graft. This second donor graft was transduced with a lentiviral vector to express the marker green fluorescence protein (“GFP”)
to allow assessment of its engraftment. CD34+ GFP marked cells were injected into untreated control mice or mice that had been treated
23 – 25 days previously with JSP191 with or without anti-CD52. After six weeks, the blood of these secondarily transplanted mice
was evaluated for evidence of GFP-marked second donor cells.
Figure
6: JSP191 in addition to an anti-CD52 antibody demonstrated the highest level of engraftment. Engraftment was demonstrated by human CD45+
cells marked to express GFP.
![](https://content.edgar-online.com/edgar_conv_img/2022/03/18/0001213900-22-013592_image_010.jpg)
Mice
pre-treated with JSP191 and anti-CD52 demonstrated the highest level of engraftment, with 67% (six of nine) of human CD45+ cells also
expressing GFP. In mice treated only with JSP191, 43% (three of seven) were GFP positive. In control mice pre-treated with anti-CD52
alone, no mice (zero of seven) showed GFP expression, while one of ten (10%) control mice not given any pre-treatment showed GFP expression
(Figure 6).
We
believe that this study can serve as a preclinical proof of concept of JSP191 conditioning enhanced engraftment with CD34+ progenitor
cells in mice, suggesting it may be efficacious in an analogous clinical setting. JSP191 appeared to be particularly effective in this
setting when used along with an anti-CD52 antibody, which was used a separate lymphodepleting agent to suppress rejection by the immune
competent first allograft.
Clinical
Data for JSP191 for Severe Combined Immunodeficiency
We have an ongoing Phase 1/2 dose escalation open
label clinical trial to evaluate JSP191 as the sole conditioning agent to achieve HSC engraftment in patients undergoing transplant for
SCID. The primary endpoint in Phase 1 is to assess the safety and tolerability of JSP191 as a conditioning agent in SCID patients. The
two primary efficacy endpoints in Phase 2 are the proportion of patients achieving adequate donor HSC engraftment and the proportion
of patients achieving naïve CD4+ T cell production greater than or equal to 85 cells/uL, a level expected to provide immune reconstitution,
during weeks 36 to 104 post-transplant. Secondary endpoints include durability of naïve T cell production, incidence and severity
of GvHD, hematopoietic recovery and pharmacokinetic properties of JSP191. Patients receive a single IV infusion of JSP191 on study day
0 in one of four dose cohorts: 0.1 mg/kg, 0.3 mg/kg, 0.6mg/kg or 1.0 mg/kg. Patients will be followed for five years following transplant.
This trial is currently open for enrollment at multiple clinical trial sites in the United States.
Other
studies of SCID patients have shown functional T and B cell reconstitution in patients achieving long-term myeloid donor chimerism of
at least 3%. SCID patients who fail to achieve durable donor cell engraftment from a first transplant may not be candidates for a second
transplant using current conditioning agents due to the toxicity of the conditioning regimen and fragile nature of most SCID patients.
These patients may remain on medically supportive immune therapies such as intravenous immunoglobulin (“IVIG”) or receive
an unconditioned “boost” transplant of donor cells which does not lead to sustained production of new immune cells.
We believe JSP191 has enabled immune reconstitution for patients based
on naïve CD4+ T-cell levels and has shown clinical benefit in SCID patients in a re-transplant and first transplant setting. Patients
have shown resolution of chronic infections, independence from or reduction of IVIG therapy and antibody response to vaccine challenge.
Through December 31, 2021 in this open label clinical trial, fifteen re-transplant patients and three first transplant patients have been
treated in the ongoing SCID Phase 1/2 study. Most of the transplanted patients have shown engraftment of donor cells and production of
functional immune cells over up to three years of follow up (Figure 7). No JSP191 treatment related SAEs have been reported through December
31, 2021 in this clinical trial. Since starting the study in March 2017, SAEs in seven patients have been reported, including fever, infections
and hypocalcemia. None were related to treatment as determined by the investigator. Based on initial efficacy and safety results, we opened
the clinical trial to a cohort of newly diagnosed infants undergoing stem cell transplant.
We expect to complete enrollment in the Phase 1/2 clinical trial by
mid-2023.
Figure
7: Naïve CD4 T cell production post-transplant was monitored over time in (A) a matched cohort of patients receiving no conditioning
and (B) patients receiving JSP191 single agent conditioning. JSP191 conditioning in SCID patients demonstrated durable naïve T cell
production and T cell levels consistent with immune reconstitution in five out of the first six patients by two years post-transplant.
![](https://content.edgar-online.com/edgar_conv_img/2022/03/18/0001213900-22-013592_image_011.jpg)
JSP191 as a Primary Therapeutic for Proliferative Disorders of
the Stem Cell
A transforming event in hematopoietic stem cells
can produce several different malignancies. Cancer stem cells possess qualities of self-renewal, prolonged survival, and the ability
to give rise to cells with more differentiated characteristics. The idea that cancer is primarily driven by a smaller population of stem
cells has important implications. For instance, many chemotherapies can shrink tumors or deplete downstream differentiated cells, but
if the therapies do not kill cancer stem cells, the tumor will grow back.
It has been shown that HSCs are the disease-initiating
cells in cancers like MDS, and that these pathogenic MDS HSCs outcompete normal HSCs present in the bone marrow of affected patients.
Furthermore, these disease-initiating HSCs express CD117, and anti-CD117 antibodies can target and eradicate these pathogenic cells.
This is especially significant in a disease like MDS where available therapies either lack disease-modifying activity or possess off-target
toxicity, preventing their use in older and/or fragile individuals who comprise most of the patients affected by MDS. Development of
anti-CD117 monoclonal antibodies, which might be safely used for targeting MDS clones, would represent a major step forward for this
disease.
We plan to evaluate JSP191 as a therapeutic for
certain MDS patients. The Revised International Prognostic Scoring System (“IPSS-R”) is a clinical assessment tool used to
evaluate risk and prognosis of newly diagnosed patients. Patients with IPSS-R scores of low or very low are not typically referred to
stem cell transplant due to the risk of transplant-related toxicities from current conditioning regiments, infection and GvHD outweighing
the patient’s expected survival with drug therapies. These patients typically suffer from anemia, thrombocytopenia or neutropenia
and are given drug therapies such as an erythropoiesis stimulating agent (“ESA”) to stimulate production of new cells to
correct their blood deficiency. However, these agents do not target the diseased hematopoietic stem cell and patients who become refractory
to ESA are dependent on routine blood transfusions, which is associated with poor survival. ESA refractory low or very low risk MDS patients
have few treatment options and are a clinical unmet need.
JSP191 and other anti-CD117 monoclonal antibodies
have been shown to deplete normal and diseased MDS human hematopoietic stem cells in clinical and pre-clinical studies. In studies in
non-human primates and healthy volunteers, administration of a single dose of JSP191 resulted in depletion of healthy hematopoietic stem
cells followed by recovery in approximately six weeks. Dr. Wendy Pang demonstrated at Stanford that our anti-CD117 monoclonal antibody
called JSP191 is capable of depleting MDS HSCs in vivo in a xenografted mouse model. New data from our MDS/AML trial of JSP191 as a conditioning
agent have revealed that the antibody can have a direct depletion effect on CD34+CD45-CD117+ cells prior to administration of fludarabine
or radiation. By depleting diseased and healthy hematopoietic stem cells, we believe that JSP191 may allow for preferential recovery
of healthy hematopoietic stem cells and restoration of normal hematopoiesis.
We intend to study JSP191 monotherapy in low-risk
MDS patients with documented cytopenia who are refractory to ESA therapy. We plan to run the primary treatment study under the existing
NDA for MDS/AML and anticipate enrollment to begin in this single arm clinical trial in early 2023.
JSP191
for Sickle Cell Disease (“SCD”)
SCD is an inherited blood disorder that affects
the hemoglobin protein in red blood cells that delivers oxygen to tissues and organs. Approximately 300,000 infants are born with SCD
annually worldwide, and the number of cases is expected to significantly increase. Currently, HSCT is the only cure available for SCD.
Allogeneic transplants as well as new autologous gene-edited transplants both currently rely on myeloablative conditioning with either
busulfan or melphalan. We believe JSP191 could be a significant advance for patients, replacing these current agents which are known
to be genotoxic and associated with limited efficacy and serious adverse effects, including veno-occlusive disease, infertility and secondary
malignancies. JSP191 for SCD patients will be evaluated in a clinical trial collaboration with the National Heart, Lung, and Blood Institute
(“NHLBI”). We expect this study to start enrollment in 2022.
JSP191
for Chronic Granulomatous Disease (“CGD”)
CGD is a rare, inherited disease of the immune
system that develops in infancy or early childhood and results in severe and sometimes life-threatening infections. Allogeneic hematopoietic
stem cell transplant is a proven cure for CGD. However, its use is limited because of the associated serious adverse effects and limited
efficacy of current conditioning agents used to deplete stem cells in preparation for transplantation. JSP191 for CGD patients will be
evaluated in a clinical trial collaboration with the National Institute of Allergy and Infectious Diseases (“NIAID”). We
expect this study to start enrollment in 2022.
JSP191 for GATA-2 MDS
GATA-2 MDS is a type of MDS characterized by mutations
in the GATA-2 gene resulting in complex phenotypes including increased risk of infection, deficiencies of immune cells such as B- and
NK-cells and overall poor prognosis. Allogeneic stem cell transplant may be used to cure these patients; however, use of current conditioning
agents can be difficult due to the fragile health status of these patients. JSP191-based conditioning for GATA-2 MDS patients will be
evaluated in a clinical trial collaboration with the National Cancer Institute (“NCI”). We expect this study to start enrollment
in 2022.
JSP191
for Fanconi Anemia (“FA”)
FA is a rare but serious blood disorder that prevents
the bone marrow from making sufficient new red blood cells. It can also cause the bone marrow to make abnormal blood cells. FA typically
presents at birth or early in childhood between five and ten years of age. Ultimately, it can lead to serious complications, including
bone marrow failure and severe aplastic anemia. Cancers such as AML and MDS are other possible complications. Treatment may include blood
transfusions or medicine to create more red blood cells, but HSCT is the only cure. JSP191 for FA patients will be evaluated in a clinical
trial collaboration with Stanford University. This study has started patient enrollment.
JSP191
for Gene Therapy
Every
gene therapy in academia or industry that modifies HSCs also requires pre-transplant conditioning to make space in the patient’s
bone marrow for the gene therapy to engraft. These types of gene therapies address a broad range of disease including heme disorders
(e.g., SCD, beta thalassemia, FA), immune disorders (e.g., SCID, CGD, leukocyte adhesion deficiency), lysosomal storage disorders (e.g.,
Fabry, Gaucher, Pompe), neurologic disorders (e.g., frontotemporal dementia, amyotrophic lateral sclerosis) and bone disorders (e.g.,
infant malignant osteoporosis) to name a few. Toxic alkylators like busulfan are still the standard conditioning regimens on which these
gene therapies rely. As a result, their curative benefit is limited to patients that can tolerate the conditioning. Furthermore, gene
therapy trials have also been halted by the FDA due to secondary malignancies discovered in study patients, which is a well-known risk
of genotoxic conditioning.
![](https://content.edgar-online.com/edgar_conv_img/2022/03/18/0001213900-22-013592_image_012.jpg)
We are collaborating with corporate
partners, including Graphite Bio, Aruvant Sciences and Avrobio, to study JSP191 as targeted, non-toxic conditioning for investigational
gene therapies. With Graphite Bio, JSP191 is being studied as conditioning prior to GPH201 gene replacement therapy for patients with
X-SCID. X-SCID is a severe, inherited disorder of the immune system with symptoms often presenting in early infancy, including persistent
infections and failure to thrive. Without treatment, X-SCID is typically fatal to patients in the first two years of life. With Aruvant
Sciences, JSP191 is being studied as conditioning prior to ARU-1801 gene therapy for patients with SCD. With Avrobio, JSP191 is being
studied as conditioning prior to gene therapy for patients with Gaucher disease.
JSP191 for Autoimmune Disorders
Autologous stem cell transplantation for inducing
remission and curing severe and refractory autoimmune diseases is relatively well established, but limitations still exist around toxicity
and transplanted-related death. We believe JSP191 can address current challenges through targeted and safer conditioning for autoimmune
disease patients. We are evaluating options for a clinical study of a JSP191-based conditioning regimen for patients with severe refractor
autoimmune diseases.
Engineered
Hematopoietic Stem Cell (eHSC) Therapy
Our eHSC platform includes multiple approaches
to developing product candidates that are currently in preclinical development and are designed to overcome key limitations of allogeneic
and autologous gene-edited stem cell grafts. By using mRNA delivery or gene editing we believe we can reprogram allogeneic donor or gene-edited
stem cells to have a transient proliferative and survival advantage, potentially leading to higher engraftment rates and reduced or eliminated
GvHD by elimination of co-transplanted donor immune cells in allogeneic transplants.
We
are evaluating multiple approaches to use mRNA to increase engraftment of HSCs. One approach is to increase expression of CXCR4, a cell
surface protein involved in cellular homing to the bone marrow. Another approach is to use mRNA to transiently increase expression of
known variants of the stem cell factor receptor that signal independent of ligand (stem cell factor) concentration. Another approach
in preclinical development is to use mRNA delivery or gene editing to express a variant of the stem cell factor receptor that is resistant
to JSP191. We are also working on other approaches to increase stem cell competitiveness that are not related to stem cell factor receptor
signaling or cellular homing.
Initial in vitro experimental results in human
cell lines show that expression of a constitutively active variant of the stem cell factor receptor can lead to cell line proliferation
independent of stem cell factor concentration. In addition, these variant cells are not affected by JSP191 since the engineered cells
proliferate independent of receptor signaling. Other in vitro experiments have shown that mRNA can be used to express these receptor
variants and other target proteins, such as CXCR4, transiently on the cell surface. We have also identified potential receptor modifications
that will keep stem cell factor binding intact but decrease or eliminate JSP191 binding.
In
the setting of autologous gene edited stem cells, these technologies could lead to faster and more complete engraftment of edited
cells without the need for toxic conditioning. Depending on the Jasper technology used, additional infusions of gene modified cells may
potentially be given to patients with low or fading responses to target protein production.
In the setting of allogeneic transplant, pure
stem cell grafts can be used in place of today’s replete or modified grafts. Similar to the autologous setting, we believe these
technologies can lead to faster and more complete engraftment of donor stem cells without the need for toxic conditioning. In addition,
by eliminating the need for donor passenger lymphocytes to drive engraftment, we can potentially eliminate the risk of GvHD and the need
for long-term immune suppression. If approved, this approach may also increase the potential for use of partially matched grafts and
expand the potential donor pool available for any given patient.
We are planning to present in-vivo data on the
eHSC program in 2022 and plan to file an IND in 2023.
![](https://content.edgar-online.com/edgar_conv_img/2022/03/18/0001213900-22-013592_image_013.jpg)
Opportunity
Areas
There
are other conditions and potential applications for JSP191 and the eHSC program. We have assessed the existing stem cell transplant market
and potential eligible patient population on a per-indication basis to estimate the potential number of patients that could benefit from
our product candidates.
Hematopoietic
Stem Cell-Based Gene Therapies
The
combination of stem cell transplantation and gene therapy has shown the potential to correct pathological genetic mutations but also
the same limitations as unmodified stem cell transplantation, which include the toxicities of current conditioning agents. Furthermore,
stem cell gene therapy requires larger doses of genetically modified stem cells for proper engraftment. We believe our product candidates
can improve the field of stem cell gene therapy and address currently identified challenges.
In
the United States alone, over 100,000 patients suffer from SCD, while about 52,000 patients are affected in the major markets in Europe.
Approximately 58,000 patients from this pool are eligible for HSCT or gene therapy as they have severe SCD.
Approximately
2,700 patients in the United States suffer from beta-thalassemia and about 16,000 in the European Union suffer from it annually. Approximately
70% of these patients can be classified to have beta-thalassemia major and, of that patient population, about 20%, or 2,600 patients,
are eligible for stem cell transplant.
License
Agreements with Amgen
In
November 2019, we entered into a worldwide exclusive license agreement with Amgen for JSP191 (formerly AMG 191) that also includes translational
science and materials from Stanford University. We were assigned and accepted Amgen’s rights and obligations, effective November
21, 2019, for the Investigator Sponsored Research Agreement (“ISRA”), entered into in June 2013, between Amgen and The
Board of Trustees of the Leland Stanford Junior University (“Stanford”) and Quality Agreement between Amgen and Stanford,
effective as of October 7, 2015. Under the ISRA, we received an option to negotiate a definitive license with Stanford for rights to
certain Stanford intellectual property related to the study of JSP191 in exchange for an option exercise fee of $1.0 million, payable
over a two-year period (the “Option”). We exercised the Option to Stanford docket S06-265 “Antibody-based clearance
of endogenous stem cell niches prior to transplantation of bone marrow or hematopoietic stem cells (c-kit)” granted by Stanford
under the ISRA on June 2, 2020. As a result, we have worldwide exclusive rights to develop and commercialize JSP191. The issued U.S.
patents would be expected to expire in 2027, absent any applicable patent term extensions.
License
Agreements with Stanford
In
March 2021, we entered into an exclusive license agreement with respect to the use of JSP191 from the Stanford Office of Technology Licensing
to license U.S. Patent Application Serial Number 60/856,435, filed Nov. 3, 2006, and U.S. Patent Application Serial Number 12/447,634
(publication number US 2010/0226927 Al) and Know How for the purpose of depleting endogenous blood stem cells in patients for whom hematopoietic
cell transplantation is indicated.
Intellectual
Property
Our
success depends in part on our ability to obtain and maintain proprietary protection for our product candidates and other discoveries,
inventions, trade secrets and know-how that are critical to our business operations. It also depends in part on our ability to operate
without infringing the proprietary rights of others, and in part, on our ability to prevent others from infringing our proprietary rights.
We have a series of in-licensed patents outlined below with an additional pending patent application in the United States.
In-licensed
Amgen Portfolio
We have exclusively licensed a patent family from Amgen applicable
to our targeted conditioning program that contains patents and applications directed to humanized c-kit antibody. As of March 8, 2022,
this patent portfolio includes three issued U.S. patents and one European patent, as well as granted patents in Australia, Canada, Japan,
and Mexico, and pending patent applications in Europe and Hong Kong. The issued U.S. and European patents would be expected to expire
in 2027, absent any applicable patent term extensions.
In-licensed
Stanford Portfolio
We have an exclusive license in the field of use of
depleting endogenous blood stem cells in patients for whom hematopoietic cell transplantation is indicated to a patent family from Stanford
University applicable to targeted conditioning that contains patents and applications directed to immunodepletion of endogenous stem cell
niche prior to hematopoietic stem cell transplantation. As of March 8, 2022, this patent portfolio includes one issued U.S. patent and
two European patents, as well as pending U.S. and European patent applications. The issued U.S. and European patents would be expected
to expire in 2027, absent any applicable patent term extensions.
Jasper Portfolio
We own four patent families directed to compositions
and/or methods for hematopoietic stem cell transplantation, and one patent family directed to other methods of treating certain hematopoietic
malignancies. These patent families include U.S. provisional applications and one PCT application. Any patents that grant from these applications
would be expected to expire in 2042 or 2043, absent any applicable patent term extensions.
Additional
Intellectual Property
We
also rely on trade secrets, including know-how, confidential information, unpatented technologies and other proprietary information,
to strengthen or enhance our competitive position, and prevent competitors from reverse engineering or copying our technologies. We maintain,
as trade secrets, information relating our product candidates currently in development, as well as information related to our business
strategy and business methods. However, trade secrets and confidential know-how are difficult to protect. To avoid inadvertent and improper
disclosure of trade secrets, and to avoid the risks of former employees using these trade secrets to gain future employment, it is our
policy to require employees, consultants and independent contractors to assign to us all rights to intellectual property they develop
in connection with their employment with or services for us. We also protect our existing and developing intellectual property expressly
through confidentiality provisions in agreements with third parties. There can be no assurance, however, that these agreements will be
self-executing or otherwise provide meaningful protection for our trade secrets or other intellectual property or proprietary information,
or adequate remedies in the event of unauthorized use or disclosure of such trade secrets or other intellectual property or proprietary
information. We also seek to preserve the integrity and confidentiality of our trade secrets and other confidential information by maintaining
physical security of our premises and physical and electronic security of our information technology systems. While we have confidence
in the measures we take to protect and preserve our trade secrets, such measures can be breached, and we may not have adequate remedies
for any such breach. In addition, our trade secrets may otherwise become known or be independently discovered by competitors.
We
intend to pursue additional intellectual property protection to the extent we believe it would advance our business objectives, which
may include objectives within and outside the United States. Despite our efforts to protect our intellectual property rights these rights
may not be respected in the future or may be circumvented or challenged (and potentially invalidated) in a legal proceeding in any jurisdiction
where we have intellectual property rights. In addition, the laws of various foreign countries may not afford the same protections or
assurances to the same extent as the laws in the United States. See the section titled “Risk Factors — Risks Related to Our
Intellectual Property” for additional information regarding these and other risks related to intellectual property.
Competition
The
industry we operate is in highly competitive and dynamic, subject to rapid technological change. We have competition in the market for
both our product candidates and may face competition from large pharmaceutical and biotechnology companies, smaller pharmaceutical and
biotechnology companies, specialty pharmaceutical companies, generic drug companies, academic institutions, government agencies, research
institutions and others. We believe that our intellectual property, proprietary scientific knowledge, development experience and partnerships
will provide us with competitive advantages in the market we operate in.
We
are aware of competing stem cell transplant and conditioning products and adjacent therapies, not limited to small molecules, biologics
and cell therapies, that address the same domain of conditions we are targeting. The following list of competitors indicate companies
that are directly competing with our two product candidates.
Competitors
for our JSP191 CD117 targeted conditioning program include the following:
| ● | Magenta
Therapeutics, Inc., which is developing an antibody drug conjugate with an antibody to CD117
linked to an amanitin toxic payload; |
| ● | Gilead
Sciences, Inc., which is developing an antibody to CD117 that may be used in combination
with an antibody to CD47; |
| ● | Actinium
Pharmaceuticals, Inc., which is developing an antibody to CD45 that is fused to iodine-131
radioisotope; |
| ● | Celldex
Therapeutics, Inc., which is developing an antibody to inhibit tyrosine kinase KIT found
in mast cells and is being studied in mast cell diseases; and |
| ● | Molecular
Templates Inc., which is developing an antibody to CD45 that is fused to an engineered Shiga-like
toxin. |
Competitors
for our engineered stem cell therapy program include the following:
| ● | Vor
Biopharma, Inc., which is developing treatment-resistant marrow cells that enable CD33 targeted
therapy; |
| ● | Sana
Biotechnology, Inc., which is developing hypoimmune cells designed to evade rejection and
enable persistence of differentiated cells; |
| ● | Ensoma
Inc., which is developing viral vectors for delivery of cell modification payload in vivo; |
| ● | Orca
Bio, which is developing precision allogeneic cell therapy products meant to safely and effectively
replace a patient’s blood and immune system; and |
| ● | Talaris
Therapeutics, Inc., which aims to remove the need for immunosuppression for solid organ transplantation
recipient with a facilitated allogeneic stem cell therapy. |
Sales
and Marketing
We
do not currently have sales and marketing infrastructure to support commercial launch of our product candidates, if approved. We may
build such capabilities in North America prior to potential launch of JSP191. Outside of North America, we may rely on licensing, co-sale
and co-promotion agreements with strategic partners for the commercialization of our product candidates. If we build a commercial infrastructure
to support marketing in North America, such commercial infrastructure could be expected to include a targeted sales force supported by
sales management, internal sales support, an internal marketing group and distribution support. To develop the appropriate commercial
infrastructure internally, we would have to invest financial and management resources, some of which would have to be deployed prior
to any confirmation that JSP191 will be approved.
Research
and Development
We
invest significantly in our research and development efforts, to discover and validate therapeutics while improving our processes and
approach to drug making. We strive to progress candidates that can address unmet or underserved clinical needs and favor programs with
well-validated targets and defined regulatory approval paths. Our R&D team has played key roles in discovering and developing a number
of promising candidates over the past 20 plus years while at Jasper, and while at Johnson & Johnson, AstraZeneca, Bristol-Myers Squibb,
Portola, Allergan, Sanofi, Amgen, Alexion and others. They have leveraged experience, insights and capabilities to optimize development,
along with fostering collaboration with external partners to innovate and expand into potential additional indications. Our current development-stage
portfolio consists of two product candidates discovered through collaboration and our internal research efforts.
Manufacturing
We
do not currently own or operate any manufacturing facility. We rely on contract manufacturing organizations (“CMOs”) to produce
our drug candidates in accordance with cGMP regulations for use in our clinical studies. The manufacture of pharmaceuticals is subject
to extensive cGMP regulations, which impose various procedural and documentation requirements and govern all areas of record keeping,
production processes and controls, personnel and quality control. Under our license agreement with Amgen, we have received a substantial
amount of drug product to support initiation of our planned clinical trials of JSP191. In November 2019, we entered into development
and manufacturing agreements with Lonza relating to the manufacturing of JSP191 and product quality testing. The facility of Lonza in
Slough, United Kingdom is responsible for production and testing of drug substance. The facility of Lonza in Stein, Switzerland is responsible
for production and testing of drug product. Labelling, packaging and storage of finished drug product is provided by PCI Pharma Services,
in San Diego, California.
Government
Regulation
Government
authorities in the United States, at the federal, state and local level, and in other countries and jurisdictions, including the European
Union, extensively regulate, among other things, the research, development, testing, manufacture, pricing, reimbursement, sales, quality
control, approval, packaging, storage, recordkeeping, labeling, advertising, promotion, distribution, marketing, post-approval monitoring
and reporting, and import and export of pharmaceutical products, including biological products. The processes for obtaining marketing
approvals in the United States and in foreign countries and jurisdictions, along with subsequent compliance with applicable statutes
and regulations and other regulatory authorities, require the expenditure of substantial time and financial resources.
Licensure
and Regulation of Biologics in the United States
In
the United States, our product candidates are regulated as biological products, or biologics, under the Public Health Service Act (“PHSA”)
and the Food, Drug, and Cosmetic Act (“FDCA”) and its implementing regulations and guidance. The failure to comply with the
applicable U.S. requirements at any time during the product development process, including preclinical testing, clinical testing, the
approval process, or post-approval process, may subject an applicant to delays in the conduct of the study, regulatory review, and approval,
and/or administrative or judicial sanctions.
An
applicant seeking approval to market and distribute a new biologic in the United States generally must satisfactorily complete each of
the following steps:
| ● | preclinical
laboratory tests, animal studies, and formulation studies all performed in accordance with
the FDA’s good laboratory practice (“GLP”) regulations; |
| ● | completion
of the manufacture, under cGMP conditions, of the drug substance and drug product that the
sponsor intends to use in human clinical trials along with required analytical and stability
testing; |
| ● | submission
to the FDA of an IND application for human clinical testing, which must become effective
before human clinical trials may begin; |
| ● | approval
by an IRB representing each clinical site before each clinical trial may be initiated; |
| ● | performance
of adequate and well-controlled human clinical trials to establish the safety, potency, and
purity of the product candidate for each proposed indication, in accordance with cGCPs; |
| ● | preparation
and submission to the FDA of a biologics license application (“BLA”) for a biologic
product requesting marketing for one or more proposed indications, including submission of
detailed information on the manufacture and composition of the product in clinical development
and proposed labelling; |
| ● | review
of the product by an FDA advisory committee, where appropriate or if applicable; |
| ● | satisfactory
completion of one or more FDA inspections of the manufacturing facility or facilities, including
those of third parties, at which the product, or components thereof, are produced to assess
compliance with cGMP requirements and to assure that the facilities, methods, and controls
are adequate to preserve the product’s identity, strength, quality, and purity; |
| ● | satisfactory
completion of any FDA audits of the preclinical studies and clinical trial sites to assure
compliance with GLP, as applicable, and good clinical practices (“GCP”), and
the integrity of clinical data in support of the BLA; |
| ● | payment
of user Prescription Drug User Fee Act (“PDUFA”) securing FDA approval of the
BLA and licensure of the new biologic product; and |
| ● | compliance
with any post-approval requirements, including the potential requirement to implement a Risk
Evaluation and Mitigation Strategy (“REMS”) and any post-approval studies or
other post-marketing commitments required by the FDA. |
Preclinical
Studies and Investigational New Drug Application
Before
testing any biologic product candidate in humans, the product candidate must undergo preclinical testing. Preclinical tests include laboratory
evaluations of product chemistry, formulation and stability, as well as studies to evaluate the potential for efficacy and toxicity in
animal studies. The conduct of the preclinical tests and formulation of the compounds for testing must comply with federal regulations
and requirements. The results of the preclinical tests, together with manufacturing information and analytical data, are submitted to
the FDA as part of an IND application.
An
IND is an exemption from the FDCA that allows an unapproved product candidate to be shipped in interstate commerce for use in an investigational
clinical trial and a request for FDA authorization to administer such investigational product to humans. The IND automatically becomes
effective 30 days after receipt by the FDA, unless before that time the FDA raises concerns or questions about the product or conduct
of the proposed clinical trial, including concerns that human research subjects will be exposed to unreasonable health risks. In that
case, the IND sponsor and the FDA must resolve any outstanding FDA concerns before the clinical trials can begin or recommence.
As
a result, submission of the IND may result in the FDA not allowing the trials to commence or allowing the trial to commence on the terms
originally specified by the sponsor in the IND. If the FDA raises concerns or questions either during this initial 30-day period, or
at any time during the IND review process, it may choose to impose a partial or complete clinical hold. Clinical holds are imposed by
the FDA whenever there is concern for patient safety, may be a result of new data, findings, or developments in clinical, preclinical,
and/or chemistry, manufacturing, and controls or where there is non-compliance with regulatory requirements. This order issued by the
FDA would delay either a proposed clinical trial or cause suspension of an ongoing trial, until all outstanding concerns have been adequately
addressed and the FDA has notified the company that investigations may proceed. This could cause significant delays or difficulties in
completing our planned clinical trial or future clinical trials in a timely manner.
Human
Clinical Trials in Support of a BLA
Clinical
trials involve the administration of the investigational product candidate to healthy volunteers or patients with the disease or condition
to be treated under the supervision of a qualified principal investigator in accordance with GCP requirements. Clinical trials are conducted
under protocols detailing, among other things, the objectives of the trial, inclusion and exclusion criteria, the parameters to be used
in monitoring safety, and the effectiveness criteria to be evaluated. A protocol for each clinical trial and any subsequent protocol
amendments must be submitted to the FDA as part of the IND.
A
sponsor who wishes to conduct a clinical trial outside the United States may, but need not, obtain FDA authorization to conduct the clinical
trial under an IND. When a foreign clinical trial is conducted under an IND, all FDA IND requirements must be met unless waived. When
a foreign clinical trial is not conducted under an IND, the sponsor must ensure that the trial complies with certain regulatory requirements
of the FDA in order to use the trial as support for an IND or application for marketing approval. Specifically, the FDA requires that
such trials be conducted in accordance with GCP, including review and approval by an independent ethics committee and informed consent
from participants. The GCP requirements encompass both ethical and data integrity standards for clinical trials. The FDA’s regulations
are intended to help ensure the protection of human subjects enrolled in non-IND foreign clinical trials, as well as the quality and
integrity of the resulting data. They further help ensure that non-IND foreign trials are conducted in a manner comparable to that required
for clinical trials in the United States.
Further,
each clinical trial must be reviewed and approved by an IRB either centrally or individually at each institution at which the clinical
trial will be conducted. The IRB will consider, among other things, clinical trial design, patient informed consent, ethical factors,
the safety of human subjects, and the possible liability of the institution. An IRB must operate in compliance with FDA regulations.
The FDA, IRB, or the clinical trial sponsor may suspend or discontinue a clinical trial at any time for various reasons, including a
finding that the clinical trial is not being conducted in accordance with FDA requirements or that the participants are being exposed
to an unacceptable health risk. Clinical testing also must satisfy extensive GCP rules and the requirements for informed consent.
Additionally,
some clinical trials are overseen by an independent group of qualified experts organized by the clinical trial sponsor, known as a data
safety monitoring board (“DSMB”). This group may recommend continuation of the trial as planned, changes in trial conduct,
or cessation of the trial at designated check points based on certain available data from the trial to which only the DSMB has access.
Clinical
trials typically are conducted in three sequential phases, but the phases may overlap or be combined. Additional studies may be required
after approval.
| ● | Phase
1 clinical trials are initially conducted in a limited population to test the product candidate
for safety, including adverse effects, dose tolerance, absorption, metabolism, distribution,
excretion, and pharmacodynamics in healthy humans or, on occasion, in patients, such as cancer
patients. |
| ● | Phase
2 clinical trials are generally conducted in a limited patient population to identify possible
adverse effects and safety risks, evaluate the efficacy of the product candidate for specific
targeted indications and determine dose tolerance and optimal dosage. Multiple Phase 2 clinical
trials may be conducted by the sponsor to obtain information prior to beginning larger and
more costly Phase 3 clinical trials. |
| ● | Phase
3 clinical trials proceed if the Phase 2 clinical trials demonstrate that a dose range of
the product candidate is potentially effective and has an acceptable safety profile. Phase
3 clinical trials are undertaken within an expanded patient population to further evaluate
dosage, provide substantial evidence of clinical efficacy, and further test for safety in
an expanded and diverse patient population at multiple, geographically dispersed clinical
trial sites. A well-controlled, statistically robust Phase 3 trial may be designed to deliver
the data that regulatory authorities will use to decide whether or not to approve, and, if
approved, how to appropriately label a biologic; such Phase 3 studies are referred to as
“pivotal.” |
In
some cases, the FDA may approve a BLA for a product but require the sponsor to conduct additional clinical trials to further assess the
product’s safety and effectiveness after licensure. Such post-approval trials are typically referred to as Phase 4 clinical trials.
These studies are used to gain additional experience from the treatment of patients in the intended therapeutic indication and to document
a clinical benefit in the case of biologics approved under accelerated approval regulations. If the FDA approves a product while a company
has ongoing clinical trials that were not necessary for approval, a company may be able to use the data from these clinical trials to
meet all or part of any Phase 4 clinical trial requirement or to request a change in the product labeling. The failure to exercise due
diligence with regard to conducting Phase 4 clinical trials could result in withdrawal of approval for products.
Information
about applicable clinical trials must be submitted within specific timeframes to the NIH for public dissemination on its ClinicalTrials.gov
website.
Compliance
with cGMP Requirements
Before
approving a BLA, the FDA typically will inspect the facility or facilities where the product is manufactured. The FDA will not approve
an application unless it determines that the manufacturing processes and facilities are in full compliance with cGMP requirements and
adequate to assure consistent production of the product within required specifications. The PHSA emphasizes the importance of manufacturing
control for products like biologics whose attributes cannot be precisely defined.
Manufacturers
and others involved in the manufacture and distribution of products must also register their establishments with the FDA and certain
state agencies. Both domestic and foreign manufacturing establishments must register and provide additional information to the FDA upon
their initial participation in the manufacturing process. Any product manufactured by or imported from a facility that has not registered,
whether foreign or domestic, is deemed misbranded under the FDCA. Establishments may be subject to periodic unannounced inspections by
government authorities to ensure compliance with cGMPs and other laws. Inspections must follow a “risk-based schedule” that
may result in certain establishments being inspected more frequently. Manufacturers may also have to provide, on request, electronic
or physical records regarding their establishments. Delaying, denying, limiting, or refusing inspection by the FDA may lead to a product
being deemed to be adulterated.
Review
and Approval of a BLA
The
results of product candidate development, preclinical testing, and clinical trials, including negative or ambiguous results as well as
positive findings, are submitted to the FDA as part of a BLA requesting a license to market the product. The BLA must contain extensive
manufacturing information and detailed information on the composition of the product and proposed labeling as well as payment of a user
fee. Under federal law, the submission of most BLAs is subject to an application user fee. The sponsor of a licensed BLA is also subject
to an annual program fee. Certain exceptions and waivers are available for some of these fees, such as an exception from the application
fee for products with orphan designation and a waiver for certain small businesses.
The
FDA has 60 days after submission of the application to conduct an initial review to determine whether it is sufficient to accept for
filing based on the agency’s threshold determination that it is sufficiently complete to permit substantive review. Once the submission
has been accepted for filing, the FDA begins an in-depth review of the application. Under the goals and policies agreed to by the FDA
under the PDUFA, the FDA has ten months in which to complete its initial review of a standard application and respond to the applicant,
and six months for a priority review of the application. The FDA does not always meet its PDUFA goal dates for standard and priority
BLAs. The review process may often be significantly extended by FDA requests for additional information or clarification. The review
process and the PDUFA goal date may be extended by three months if the FDA requests or if the applicant otherwise provides additional
information or clarification regarding information already provided in the submission within the last three months before the PDUFA goal
date.
Under
the PHSA, the FDA may approve a BLA if it determines that the product is safe, pure, and potent, and the facility where the product will
be manufactured meets standards designed to ensure that it continues to be safe, pure, and potent. On the basis of the FDA’s evaluation
of the application and accompanying information, including the results of the inspection of the manufacturing facilities and any FDA
audits of preclinical and clinical trial sites to assure compliance with GCPs, the FDA may issue an approval letter or a complete response
letter. An approval letter authorizes commercial marketing of the product with specific prescribing information for specific indications.
If the application is not approved, the FDA will issue a complete response letter, or CRL, which will contain the conditions that must
be met in order to secure final approval of the application, and when possible will outline recommended actions the sponsor might take
to obtain approval of the application. Sponsors that receive a CRL may submit to the FDA information that represents a complete response
to the issues identified by the FDA.
The
FDA may also refer the application to an advisory committee for review, evaluation, and recommendation as to whether the application
should be approved. In particular, the FDA may refer applications for novel biologic products or biologic products that present difficult
questions of safety or efficacy to an advisory committee. Typically, an advisory committee is a panel of independent experts, including
clinicians and other scientific experts, that reviews, evaluates, and provides a recommendation as to whether the application should
be approved and under what conditions. The FDA is not bound by the recommendations of an advisory committee, but it considers such recommendations
carefully when making decisions.
If
the FDA approves a new product, it may limit the approved indication(s) for use of the product. It may also require that contraindications,
warnings, or precautions be included in the product labeling. In addition, the FDA may call for post-approval studies, including Phase
4 clinical trials, to further assess the product’s efficacy and/or safety after approval. The agency may also require testing and
surveillance programs to monitor the product after commercialization, or impose other conditions, including distribution restrictions
or other risk management mechanisms, including REMS, to help ensure that the benefits of the product outweigh the potential risks. REMS
can include medication guides, communication plans for healthcare professionals, and elements to assure safe use.
Expedited
Review Programs
The
FDA is authorized to expedite the review of BLAs in several ways. Under the Fast Track program, the sponsor of a product candidate may
request the FDA to designate the product for a specific indication as a Fast Track product concurrent with or after the filing of the
IND. Candidate products are eligible for Fast Track designation if they are intended to treat a serious or life-threatening condition
and demonstrate the potential to address unmet medical needs for the condition. Fast Track designation applies to the combination of
the product candidate and the specific indication for which it is being studied. In addition to other benefits, such as the ability to
have greater interactions with the FDA, the FDA may initiate review of sections of a Fast Track application before the application is
complete, a process known as rolling review.
Any
product candidate submitted to the FDA for marketing, including under a Fast Track program, may be eligible for other types of FDA programs
intended to expedite development and review, such as breakthrough therapy designation, priority review and accelerated approval.
| ● | Breakthrough
therapy designation. To qualify for the breakthrough therapy program, product candidates
must be intended to treat a serious or life-threatening disease or condition and preliminary
clinical evidence must indicate that such product candidates may demonstrate substantial
improvement on one or more clinically significant endpoints over existing therapies. The
FDA will seek to ensure the sponsor of a breakthrough therapy product candidate receives
intensive guidance on an efficient drug development program, intensive involvement of senior
managers and experienced staff on a proactive, collaborative and cross-disciplinary review
and rolling review. |
| ● | Priority
review. A product candidate is eligible for priority review if it treats a serious condition
and, if approved, it would be a significant improvement in the safety or effectiveness of
the treatment, diagnosis or prevention compared to marketed products. The FDA aims to complete
its review of priority review applications within six months as opposed to 10 months for
standard review. |
| ● | Accelerated
approval. Drug or biologic products studied for their safety and effectiveness in treating
serious or life-threatening illnesses and that provide meaningful therapeutic benefit over
existing treatments may receive accelerated approval. Accelerated approval means that a product
candidate may be approved on the basis of adequate and well controlled clinical trials establishing
that the product candidate has an effect on a surrogate endpoint that is reasonably likely
to predict a clinical benefit, or on the basis of an effect on a clinical endpoint other
than survival or irreversible morbidity or mortality or other clinical benefit, taking into
account the severity, rarity and prevalence of the condition and the availability or lack
of alternative treatments. As a condition of approval, the FDA may require that a sponsor
of a drug or biologic product candidate receiving accelerated approval perform adequate and
well controlled post-marketing clinical trials. In addition, the FDA currently requires as
a condition for accelerated approval pre-approval of promotional materials. |
| ● | Regenerative
advanced therapy. With passage of the 21st Century Cures Act (the “Cures Act”)
in December 2016, Congress authorized the FDA to accelerate review and approval of products
designated as regenerative advanced therapies. A product is eligible for this designation
if it is a regenerative medicine therapy that is intended to treat, modify, reverse or cure
a serious or life-threatening disease or condition and preliminary clinical evidence indicates
that the product candidate has the potential to address unmet medical needs for such disease
or condition. The benefits of a regenerative advanced therapy designation include early interactions
with the FDA to expedite development and review, benefits available to breakthrough therapies,
potential eligibility for priority review and accelerated approval based on surrogate or
intermediate endpoints. |
None
of these expedited programs change the standards for approval but they may help expedite the development or approval process of product
candidates.
Post-Approval
Regulation
If
regulatory approval for marketing of a product or new indication for an existing product is obtained, the sponsor will be required to
comply with all regular post-approval regulatory requirements as well as any post-approval requirements that the FDA have imposed as
part of the approval process. The sponsor will be required to report certain adverse reactions and production problems to the FDA, provide
updated safety and efficacy information and comply with requirements concerning advertising and promotional labeling requirements. Manufacturers
and certain of their subcontractors are required to register their establishments with the FDA and certain state agencies and are subject
to periodic unannounced inspections by the FDA and certain state agencies for compliance with ongoing regulatory requirements, including
cGMP regulations, which impose certain procedural and documentation requirements upon manufacturers. Accordingly, the sponsor and its
third-party manufacturers must continue to expend time, money, and effort in the areas of production and quality control to maintain
compliance with cGMP regulations and other regulatory requirements.
A
product may also be subject to official lot release, meaning that the manufacturer is required to perform certain tests on each lot of
the product before it is released for distribution. If the product is subject to official lot release, the manufacturer must submit samples
of each lot, together with a release protocol showing a summary of the history of manufacture of the lot and the results of all of the
manufacturer’s tests performed on the lot, to the FDA. The FDA may in addition perform certain confirmatory tests on lots of some
products before releasing the lots for distribution. Finally, the FDA will conduct laboratory research related to the safety, purity,
potency, and effectiveness of pharmaceutical products.
Once
an approval is granted, the FDA may withdraw the approval if compliance with regulatory requirements and standards is not maintained
or if problems occur after the product reaches the market. Later discovery of previously unknown problems with a product, including adverse
events of unanticipated severity or frequency, or with manufacturing processes, or failure to comply with regulatory requirements, may
result in revisions to the approved labeling to add new safety information; imposition of post-market studies or clinical trials to assess
new safety risks; or imposition of distribution or other restrictions under a REMS program. Other potential consequences include, among
other things:
| ● | restrictions
on the marketing or manufacturing of the product, complete withdrawal of the product from
the market or product recalls; |
| ● | fines,
warning letters or holds on post-approval clinical trials; |
| ● | refusal
of the FDA to approve pending applications or supplements to approved applications, or suspension
or revocation of product license approvals; |
| ● | product
recall, seizure or detention, or refusal to permit the import or export of products; or |
| ● | injunctions
or the imposition of civil or criminal penalties. |
Pharmaceutical
products may be promoted only for the approved indications and in accordance with the provisions of the approved label. Although healthcare
providers may prescribe products for uses not described in the drug’s labeling, known as off-label uses, in their professional
judgment, drug manufacturers are prohibited from soliciting, encouraging or promoting unapproved uses of a product. The FDA and other
agencies actively enforce the laws and regulations prohibiting the promotion of off-label uses, and a company that is found to have improperly
promoted off-label uses may be subject to significant liability.
The
FDA strictly regulates the marketing, labeling, advertising, and promotion of prescription drug products placed on the market. This regulation
includes, among other things, standards and regulations for direct-to-consumer advertising, communications regarding unapproved uses,
industry-sponsored scientific and educational activities, and promotional activities involving the Internet and social media. Promotional
claims about a drug’s safety or effectiveness are prohibited before the drug is approved. After approval, a drug product generally
may not be promoted for uses that are not approved by the FDA, as reflected in the product’s prescribing information.
If
a company is found to have promoted off-label uses, it may become subject to adverse public relations and administrative and judicial
enforcement by the FDA, the Department of Justice or the Office of the Inspector General of the Department of Health and Human Services,
as well as state authorities. This could subject a company to a range of penalties that could have a significant commercial impact, including
civil and criminal fines and agreements that materially restrict the manner in which a company promotes or distributes drug products.
The federal government has levied large civil and criminal fines against companies for alleged improper promotion and has also requested
that companies enter into consent decrees or permanent injunctions under which specified promotional conduct is changed or curtailed.
Regulation
and Procedures Governing Approval of Medicinal Products in the European Union
In
order to market any product outside of the United States, a company must also comply with numerous and varying regulatory requirements
of other countries and jurisdictions regarding quality, safety, and efficacy, and governing, among other things, clinical trials, marketing
authorization, commercial sales, and distribution of drug products. Whether or not it obtains FDA approval for a product, an applicant
will need to obtain the necessary approvals by the comparable foreign regulatory authorities before it can commence clinical trials or
marketing of the product in those countries or jurisdictions. Specifically, the process governing approval of medicinal products in the
European Union generally follows the same lines as in the United States. It entails satisfactory completion of preclinical studies and
adequate and well-controlled clinical trials to establish the safety and efficacy of the product for each proposed indication. It also
requires the submission to the relevant competent authorities of a marketing authorization application (“MAA”) and granting
of a marketing authorization by these authorities before the product can be marketed and sold in the European Union.
Clinical
Trial Approval
Pursuant
to Clinical Trials Directive 2001/20/EC and the Directive 2005/28/EC on GCP, a system for the approval of clinical trials in the European
Union was implemented through national legislation of the member states. Under this system, an applicant must obtain approval from the
competent national authority of a European Union member state in which the clinical trial is to be conducted, or in multiple member states
if the clinical trial is to be conducted in a number of member states. Furthermore, the applicant may only start a clinical trial at
a specific site after the competent ethics committee has issued a favorable opinion. The clinical trial application must be accompanied
by an investigational medicinal product dossier with supporting information prescribed by Directive 2001/20/EC and Directive 2005/28/EC
and corresponding national laws of the member states and further detailed in applicable guidance documents.
In
April 2014, the European Union adopted a new Clinical Trials Regulation (EU) No 536/2014, which became effective on January 31, 2022.
It overhauled the current system of approvals for clinical trials in the European Union. Specifically, the new legislation, which is
directly applicable in all member states, is aimed at simplifying and streamlining the approval of clinical trials in the European Union.
For instance, the new Clinical Trials Regulation provides for a streamlined application procedure via a single-entry point, the Clinical
Trials Information System (“CTIS”), and strictly defined deadlines for the assessment of clinical trial applications.
The
conduct of all clinical trials commenced in the European Union prior to January 31, 2022 will continue to be bound by the previously
applicable provisions. However, if a clinical trial continues for more than three years after January 31, 2022, the Clinical Trials Regulation
will at that time begin to apply to the clinical trial. In addition, through January 31, 2023, clinical trial sponsors may apply for
a new trial authorization under the previously applicable provisions (posting clinical trial information at the EudraCT website) or the
Clinical Trials Regulation (posting clinical trial information at CTIS website), at the sponsor’s choice. After that date, new
trial authorizations must be applied for under the Clinical Trials Regulation and utilize CTIS.
Marketing
Authorization
To
obtain a marketing authorization for a product under the European Union regulatory system, an applicant must submit an MAA, either under
a centralized procedure administered by the EMA or one of the procedures administered by competent authorities in European Union Member
States (decentralized procedure, national procedure, or mutual recognition procedure). A marketing authorization may be granted only
to an applicant established in the European Union. Regulation (EC) No 1901/2006 provides that prior to obtaining a marketing authorization
in the European Union, an applicant must demonstrate compliance with all measures included in an EMA approved Pediatric Investigation
Plan (“PIP”) covering all subsets of the pediatric population, unless the EMA has granted a product specific waiver, class
waiver, or a deferral for one or more of the measures included in the PIP.
The
centralized procedure provides for the grant of a single marketing authorization by the European Commission that is valid for all European
Union member states. Pursuant to Regulation (EC) No. 726/2004, the centralized procedure is compulsory for specific products, including
for medicines produced by certain biotechnological processes, products designated as orphan medicinal products, advanced therapy products
and products with a new active substance indicated for the treatment of certain diseases, including products for the treatment of cancer.
For products with a new active substance indicated for the treatment of other diseases and products that are highly innovative or for
which a centralized process is in the interest of patients, the centralized procedure may be optional. Manufacturers must demonstrate
the quality, safety, and efficacy of their products to the EMA, which provides an opinion regarding the MAA. The European Commission
grants or refuses marketing authorization in light of the opinion delivered by the EMA.
Under
the centralized procedure, the CHMP established at the EMA is responsible for conducting an initial assessment of a product. Under the
centralized procedure in the European Union, the maximum timeframe for the evaluation of an MAA is 210 days, excluding clock stops when
additional information or written or oral explanation is to be provided by the applicant in response to questions of the CHMP. Accelerated
evaluation may be granted by the CHMP in exceptional cases, when a medicinal product is of major interest from the point of view of public
health and, in particular, from the viewpoint of therapeutic innovation. If the CHMP accepts such a request, the time limit of 210 days
will be reduced to 150 days, but it is possible that the CHMP may revert to the standard time limit for the centralized procedure if
it determines that it is no longer appropriate to conduct an accelerated assessment.
Coverage,
Pricing, and Reimbursement
Significant
uncertainty exists as to the coverage and reimbursement status of any product candidates for which we may seek regulatory approval by
the FDA or other government authorities. In the United States and markets in other countries, patients who are prescribed treatments
for their conditions and providers performing the prescribed services generally rely on third-party payors to reimburse all or part of
the associated healthcare costs. Patients are unlikely to use any product candidates we may develop unless coverage is provided and reimbursement
is adequate to cover a significant portion of the cost of such product candidates. Even if any product candidates we may develop are
approved, sales of such product candidates will depend, in part, on the extent to which third-party payors, including government health
programs in the United States such as Medicare and Medicaid, commercial health insurers, and managed care organizations, provide coverage,
and establish adequate reimbursement levels for, such product candidates. The process for determining whether a payor will provide coverage
for a product may be separate from the process for setting the price or reimbursement rate that the payor will pay for the product once
coverage is approved. Third-party payors are increasingly challenging the prices charged, examining the medical necessity, and reviewing
the cost-effectiveness of medical products and services and imposing controls to manage costs. Third-party payors may limit coverage
to specific products on an approved list, also known as a formulary, which might not include all of the approved products for a particular
indication.
In
order to secure coverage and reimbursement for any product that might be approved for sale, a company may need to conduct expensive pharmacoeconomic
studies in order to demonstrate the medical necessity and cost-effectiveness of the product, in addition to the costs required to obtain
FDA or other comparable marketing approvals. Nonetheless, product candidates may not be considered medically necessary or cost-effective.
A decision by a third-party payor not to cover any product candidates we may develop could reduce physician utilization of such product
candidates once approved and have a material adverse effect on our sales, results of operations and financial condition. Additionally,
a payor’s decision to provide coverage for a product does not imply that an adequate reimbursement rate will be approved. Further,
one payor’s determination to provide coverage for a product does not assure that other payors will also provide coverage and reimbursement
for the product, and the level of coverage and reimbursement can differ significantly from payor to payor. Third-party reimbursement
and coverage may not be available to enable us to maintain price levels sufficient to realize an appropriate return on our investment
in product development. In addition, any companion diagnostic tests require coverage and reimbursement separate and apart from the coverage
and reimbursement for their companion pharmaceutical or biological products. Similar challenges to obtaining coverage and reimbursement
applicable to pharmaceutical or biological products will apply to any companion diagnostics.
The
containment of healthcare costs also has become a priority of federal, state and foreign governments and the prices of pharmaceuticals
have been a focus in this effort. Governments have shown significant interest in implementing cost-containment programs, including price
controls, restrictions on reimbursement, and requirements for substitution of generic products. Adoption of price controls and cost-containment
measures, and adoption of more restrictive policies in jurisdictions with existing controls and measures, could further limit a company’s
revenue generated from the sale of any approved products. Coverage policies and third-party reimbursement rates may change at any time.
Even if favorable coverage and reimbursement status is attained for one or more products for which a company or its collaborators receive
marketing approval, less favorable coverage policies and reimbursement rates may be implemented in the future.
If
we obtain approval in the future to market in the United States any product candidates we may develop, we may be required to provide
discounts or rebates under government healthcare programs or to certain government and private purchasers in order to obtain coverage
under federal healthcare programs such as Medicaid. Participation in such programs may require us to track and report certain drug prices.
We may be subject to fines and other penalties if we fail to report such prices accurately.
Outside
the United States, ensuring adequate coverage and payment for any product candidates we may develop will face challenges. Pricing of
prescription pharmaceuticals is subject to governmental control in many countries. Pricing negotiations with governmental authorities
can extend well beyond the receipt of regulatory marketing approval for a product and may require us to conduct a clinical trial that
compares the cost-effectiveness of any product candidates we may develop to other available therapies. The conduct of such a clinical
trial could be expensive and result in delays in our commercialization efforts.
In
the European Union, pricing and reimbursement schemes vary widely from country to country. Some countries provide that products may be
marketed only after a reimbursement price has been agreed. Some countries may require the completion of additional studies that compare
the cost-effectiveness of a particular product candidate to currently available therapies (so called health technology assessments) in
order to obtain reimbursement or pricing approval. For example, the European Union provides options for its member states to restrict
the range of products for which their national health insurance systems provide reimbursement and to control the prices of medicinal
products for human use. European Union member states may approve a specific price for a product, or they may instead adopt a system of
direct or indirect controls on the profitability of the company placing the product on the market. Other member states allow companies
to fix their own prices for products but monitor and control prescription volumes and issue guidance to physicians to limit prescriptions.
Recently, many countries in the European Union have increased the amount of discounts required on pharmaceuticals and these efforts could
continue as countries attempt to manage healthcare expenditures, especially in light of the severe fiscal and debt crises experienced
by many countries in the European Union. The downward pressure on healthcare costs in general, particularly prescription products, has
become intense. As a result, increasingly high barriers are being erected to the entry of new products. Political, economic, and regulatory
developments may further complicate pricing negotiations, and pricing negotiations may continue after reimbursement has been obtained.
Reference pricing used by various European Union member states, and parallel trade (arbitrage between low-priced and high-priced member
states), can further reduce prices. There can be no assurance that any country that has price controls or reimbursement limitations for
pharmaceutical products will allow favorable reimbursement and pricing arrangements for any of our products, if approved in those countries.
Healthcare
Law and Regulation
Healthcare
providers and third-party payors play a primary role in the recommendation and prescription of drug products that are granted marketing
approval. Arrangements with providers, consultants, third-party payors, and customers are subject to broadly applicable fraud and abuse,
anti-kickback, false claims laws, patient privacy laws and regulations and other healthcare laws and regulations that may constrain our
business and/or financial arrangements. Restrictions under applicable federal and state healthcare laws and regulations, include the
following:
| ● | the
U.S. federal Anti-Kickback Statute, which prohibits, among other things, persons and entities
from knowingly and willfully soliciting, offering, paying, receiving, or providing remuneration,
directly or indirectly, in cash or in kind, to induce or reward either the referral of an
individual for, or the purchase, order or recommendation of, any good or service, for which
payment may be made, in whole or in part, under a federal healthcare program such as Medicare
and Medicaid; |
| ● | the
federal civil and criminal false claims laws, including the civil False Claims Act, and civil
monetary penalties laws, which prohibit individuals or entities from, among other things,
knowingly presenting, or causing to be presented, to the federal government, claims for payment
that are false, fictitious, or fraudulent or knowingly making, using, or causing to made
or used a false record or statement to avoid, decrease, or conceal an obligation to pay money
to the federal government; |
| ● | the
FCPA, which prohibits companies and their intermediaries from making, or offering or promising
to make improper payments to non-U.S. officials for the purpose of obtaining or retaining
business or otherwise seeking favorable treatment; and |
| ● | the
federal transparency requirements known as the federal Physician Payments Sunshine Act, which
requires certain manufacturers of drugs, devices, biologics and medical supplies to report
annually to the CMS within the U.S. Department of Health and Human Services, information
related to payments and other transfers of value made by that entity to physicians, as defined
by such law, and teaching hospitals, as well as ownership and investment interests held by
physicians and their immediate family members. |
Further,
some state laws require pharmaceutical companies to comply with the pharmaceutical industry’s voluntary compliance guidelines and
the relevant compliance guidance promulgated by the federal government in addition to requiring pharmaceutical manufacturers to report
information related to payments to physicians and other healthcare providers or marketing expenditures. In addition, certain state and
local laws require the registration of pharmaceutical sales representatives in the jurisdiction. State and foreign laws also govern the
privacy and security of health information in some circumstances, many of which differ from each other in significant ways and often
are not preempted by the federal Health Insurance Portability and Accountability Act of 1996 (“HIPAA”), thus complicating
compliance efforts.
Employees
and Human Capital
As of December 31, 2021, we employed 25 full-time
employees. The 25 full-time employees were engaged in research and development, operations, finance, and business development. Nine employees
held Ph.D. degrees; two held M.D. degrees; and one held a VMD. Our employees are not represented by labor unions or covered under any
collective bargaining agreements. We consider our relationship with our employees to be good.
Our
human capital resources objectives include, as applicable, identifying, recruiting, retaining, incentivizing and integrating our existing
and additional employees. The principal purposes of our equity incentive plans are to attract, retain and motivate selected employees,
consultants and directors through the granting of stock-based compensation awards.
Facilities
We
lease approximately 13,392 square feet of space for our headquarters in Redwood City, California under an agreement that expires in August
2026. Thereafter, at our option, we may extend the term for an additional five years to August 2031. We believe that our existing
facilities are adequate to meet our current needs, and that suitable additional alternative spaces will be available in the future
on commercially reasonable terms.
Indemnification
and Insurance
Our
business exposes us to potential liability including, but not limited to, potential liability for (i) non-compliance with applicable
laws and regulations, and (ii) employment-related claims. In certain circumstances, we may also be liable for the acts or omissions of
others, such as suppliers of goods or services.
We
attempt to manage our potential liability to third parties through contractual protection (such as indemnification and limitation of
liability provisions) in our contracts and through insurance. The contractual indemnification provisions vary in scope and generally
do not protect us against all potential liabilities. In addition, in the event that we seek to enforce such an indemnification provision,
the indemnifying party may not have sufficient resources to fully satisfy its indemnification obligations or may otherwise not comply
with its contractual obligations.
We
currently maintain insurance coverage with limits we believe to be appropriate. The coverage provided by such insurance may not be adequate
for all claims made, and such claims may be contested by applicable insurance carriers.
Organization
We were organized as a corporation under the laws
of the State of Delaware on August 13, 2019 under the name “Amplitude Healthcare Acquisition Corporation”. On September 24,
2021, we consummated the previously announced Business Combination (pursuant to the Business Combination Agreement, dated May 5, 2021,
by and among AMHC, Merger Sub and Old Jasper). Pursuant to the terms of the Business Combination Agreement, a Business Combination or
Reverse Recapitalization for accounting purposes between AMHC and Old Jasper was effected through the merger of Merger Sub with and into
Old Jasper with Old Jasper surviving as AMHC’s wholly-owned subsidiary. In connection with the Business Combination, AMHC changed
its name from Amplitude Healthcare Acquisition Corporation to Jasper Therapeutics, Inc.
Website
Access to SEC Filings
We
file annual, quarterly and special reports, proxy statements and other information with the SEC. The SEC maintains an Internet website
at http://www.sec.gov that contains reports, proxy and information statements, and other information regarding issuers that file electronically
with the SEC, including Jasper. We maintain an Internet website at www.jaspertherapeutics.com. The information contained on our website
or that can be accessed through our website does not constitute a part of this report. We make available, free of charge through our
Internet website, our Annual Reports on Form 10-K, Quarterly Reports on Form 10-Q, Current Reports on Form 8-K and amendments
to those reports filed or furnished pursuant to Section 13(a) or 15(d) of the Exchange Act, as soon as reasonably practicable after
we electronically file or furnish this information to the SEC.
ITEM
1A. RISK FACTORS
Investing
in our common stock involves a high degree of risk. Before making an investment decision, you should carefully consider the risks described
below before deciding whether to invest in our common stock. Before you make a decision to buy our securities, in addition to the risks
and uncertainties discussed above under “Cautionary Note Regarding Forward-Looking Statements”, you should carefully
consider the specific risks set forth herein. If any of these risks actually occur, it may materially harm our business, financial condition,
liquidity and results of operations. As a result, the market price of our securities could decline, and you could lose all or part of
your investment. Additionally, the risks and uncertainties described below are not the only risks and uncertainties that we face. Additional
risks and uncertainties not presently known to us or that we currently believe to be immaterial may become material and adversely affect
our business.
Risk
Factor Summary
Below
is a summary of the principal factors that make an investment in our common stock speculative or risky. This summary does not address
all of the risks that we face. Additional discussion of the risks summarized in this risk factor summary, and other risks that we face,
can be found below and should be carefully considered, together with other information in this Annual Report on Form 10-K and our other
filings with the SEC before making an investment decision regarding our common stock.
|
● |
Risks Related to Our Financial Position and Need for
Additional Capital, including, among others, that: |
|
● |
We have incurred significant net losses and negative
operating cash flows since our inception. We expect to incur net losses for the foreseeable future and may never achieve or maintain
profitability. |
|
● |
We will need substantial additional funding. If we
are unable to raise capital when needed, we would be forced to delay, reduce or eliminate our research and product development programs
or future commercialization efforts. |
|
● |
As a result of our history of losses and negative cash
flows from operations, our consolidated financial statements contain a statement regarding a substantial doubt about our ability
to continue as a going concern. |
|
● |
Risks Related to Discovery, Development, Manufacturing
and Commercialization, including, among others, that: |
|
● |
We are substantially dependent on the success of our
most advanced product candidate, JSP191. If we are unable to complete development of, obtain approval for and commercialize our product
candidates, including JSP191, in a timely manner or at all, our business will be harmed. |
|
● |
We may not be successful in our efforts to identify,
develop and commercialize additional product candidates. If these efforts are unsuccessful, we may never become a commercial stage
company or generate any revenues. |
|
● |
eHSCs are a novel technology that is not yet clinically
validated for human use. The approaches we are taking to create eHSCs are unproven and may never lead to marketable products. |
|
● |
If any of our product candidates cause serious adverse
events, undesirable side effects or unexpected characteristics, such events, side effects or characteristics could delay or prevent
regulatory approval of the product candidate, limit our commercial potential or result in significant negative consequences following
any potential marketing approval. |
|
● |
Results of preclinical studies and early clinical trials
may not be predictive of results of future clinical trials, and such results do not guarantee approval of a product candidate by
regulatory authorities. In addition, our clinical trials to date have been limited in scope, and results received to date may not
be replicated in expanded or additional future clinical trials. |
|
● |
We have never obtained regulatory approval for a drug,
may never receive regulatory approval for any of our product candidates, and may therefore never generate revenues from product sales. |
|
● |
We face significant competition in an environment of
rapid technological change, and there is a possibility that our competitors may achieve regulatory approval before us or develop
therapies that are safer or more advanced or effective than ours, which may harm our financial condition and our ability to successfully
market or commercialize our product candidates. |
|
● |
Risks
Related to Regulatory Review, including, among others, that: |
|
● |
If clinical trials of our product
candidates fail to demonstrate safety and efficacy to the satisfaction of regulatory authorities or do not otherwise produce positive
results, we may incur additional costs or experience delays in completing, or ultimately be unable to complete, the development and
commercialization of such product candidates. |
|
● |
Stem cell transplant is a high-risk procedure
with curative potential that may result in complications or adverse events for patients in our clinical trials or for patients that
use any of our product candidates, if approved. |
|
● |
Risks Related to Our Relationships
with Third Parties, including, among others, that: |
|
● |
We rely on third parties to
conduct our preclinical and clinical trials and will rely on them to perform other tasks for us. If these third parties do not successfully
carry out their contractual duties, meet expected deadlines or comply with regulatory requirements, we may not be able to obtain
regulatory approval for or commercialize our product candidates and our business could be substantially harmed. |
|
● |
We currently rely on a single
manufacturer for our clinical supply of our product candidates. In the event of a loss of this manufacturer, or a failure by
such manufacturer to comply with the U.S. Food and Drug Administration (“FDA”) regulations, we may not be able to
find an alternative source on commercially reasonable terms, or at all. |
|
● |
Risks Related to Our Intellectual
Property, including, among others, that: |
|
● |
We are highly dependent on
intellectual property licensed from third parties, and termination of any of these licenses could result in the loss of significant
rights, which would harm our business. |
|
● |
Our commercial success depends
on our ability to obtain, maintain and protect our intellectual property and proprietary technology. |
|
● |
Risks Related to Ownership
of Our Common Stock and Warrants, including, among others, that we will incur significant increased expenses and administrative burdens
as a public company, which could negatively impact our business, financial condition and results of operations. |
Risks
Related to Our Financial Position and Need for Additional Capital
We
have incurred significant net losses and negative operating cash flows since our inception. We expect to incur net losses for the foreseeable
future and may never achieve or maintain profitability.
We are a clinical-stage biotechnology company
dedicated to enabling cures through hematopoietic stem cell therapy and have a limited operating history. Investment in biopharmaceutical
product development is highly speculative because it entails substantial upfront capital expenditures and significant risk that any potential
product candidate will fail to demonstrate adequate effect or an acceptable safety profile, gain regulatory approval and become commercially
viable. We have no products approved for commercial sale and have not generated any revenue from product sales to date, and we continue
to incur significant research and development and other expenses related to our ongoing operations. As a result, we are not profitable
and have incurred losses and negative operating cash flows in each period since our inception. For the years ended December 31,
2021 and 2020, we reported net losses of $30.6 million and $31.7 million, respectively. For the years ended December 31,
2021 and 2020, we reported negative operating cash flows of $33.7 million and $18.3 million, respectively. As of December 31,
2021, we had an accumulated deficit of $67.5 million. We have devoted all of our efforts to organizing and staffing our company, business
and scientific planning, raising capital, acquiring and developing technology, identifying potential product candidates, undertaking
research and preclinical studies of potential product candidates, developing manufacturing capabilities and evaluating a clinical path
for our pipeline programs. We expect to continue to incur significant expenses and increasing operating losses for the foreseeable future,
and we expect these losses to increase as we continue our research and development of, and seek regulatory approvals for, our product
candidates.
The
net losses we incur may fluctuate significantly from quarter to quarter. We anticipate that our expenses will increase substantially
if and as we:
| ● | continue
the open label Phase 1/2 clinical trial for JSP191 for SCID, and the open label Phase 1
clinical trial for JSP191 in patients with MDS or AML; |
| ● | continue
the clinical development of JSP191 in autoimmune diseases and other indications; |
| ● | continue
our current research programs and development of other potential product candidates from
our current research programs; |
| ● | seek
to identify additional product candidates and research programs; |
| ● | initiate
preclinical testing and clinical trials for any other product candidates we identify and
develop; |
| ● | maintain,
expand, enforce, defend and protect our intellectual property portfolio, and provide reimbursement
of third-party expenses
related to our patent portfolio; |
| ● | seek
marketing approvals for any product candidates that successfully complete clinical trials; |
| ● | ultimately
establish a sales, marketing and distribution infrastructure to commercialize any product
candidates for which we may obtain marketing approval; |
| ● | adapt
our regulatory compliance efforts to incorporate requirements applicable to any approved
product candidates; |
| ● | further
develop our genome engineering capabilities; |
| ● | hire
additional research and development and clinical personnel; |
| ● | hire
commercial personnel and advance market access and reimbursement strategies; |
| ● | add
operational, financial and management information systems and personnel, including personnel
to support our product development; |
| ● | acquire
or in-license product
candidates, intellectual property and technologies; |
| ● | develop
or in-license manufacturing
and distribution technologies; |
| ● | should
we decide to do so and receive approval for any of our product candidates, build and maintain,
or purchase and validate, commercial-scale manufacturing
facilities designed to comply with current Good Manufacturing Practices (“cGMP”)
requirements; and |
| ● | incur
additional legal, accounting and other expenses in operating as a public company. |
As
a company, we have not completed clinical development of any product candidate and expect that it will be several years, if ever,
before we have a product candidate ready for commercialization. To become and remain profitable, we must develop and, either directly
or through collaborators, eventually commercialize a product or products with significant market potential. This will require us to be
successful in a range of challenging activities, including identifying product candidates, completing preclinical testing and clinical
trials of product candidates, obtaining marketing approval for these product candidates, manufacturing, marketing and selling those products
for which we may obtain marketing approval and satisfying any post-marketing requirements.
We
may never succeed in these activities and, even if we do, may never generate revenues that are significant or large enough to achieve
profitability. Our product candidates and research programs are currently only in the early stages of development. Because of the numerous
risks and uncertainties associated with developing product candidates, we are unable to predict the extent of any future losses or when
we will become profitable, if at all. If we do achieve profitability, we may not be able to sustain or increase profitability on a quarterly
or annual basis. Our failure to become and remain profitable would decrease the value of our company and could impair our ability to
raise capital, maintain our research and development efforts, expand our business or continue our operations. A decline in the value
of our company could also cause you to lose all or part of your investment.
We
will need substantial additional funding, which may not be available on acceptable terms, or at all. If we are unable to raise capital
when needed, we would be forced to delay, reduce or eliminate our research and product development programs or future commercialization
efforts.
We
expect to spend substantial amounts of cash to conduct further research and development and preclinical testing and clinical trials of
our product candidates, to seek regulatory approvals for our product candidates and to launch and commercialize any product candidates
for which we receive regulatory approval. Furthermore, we expect to incur additional costs associated with operating as a public company.
Accordingly, we will need to obtain substantial additional funding in order to maintain our continuing operations. If we are unable to
raise capital when needed or on attractive terms, we would be forced to delay, reduce or eliminate our research and product development
programs or future commercialization efforts. As of December 31, 2021, our cash and cash equivalents were $84.7 million and we had an
accumulated deficit of $67.5 million. Our future financing requirements will depend on many factors, including:
| ● | the
initiation, progress, timing, costs and results of preclinical studies and clinical trials
for our product candidates, including any COVID-19-related delays or other effects on
our development programs; |
| | |
| ● | the
costs of continuing to build our technology platform, including in-licensing additional
genome engineering technologies for use in developing our product candidates; |
| | |
| ● | the
costs of developing, acquiring or in-licensing additional targeted therapies to use
in combination with JSP191 and other product candidates we may develop; |
| | |
| ● | the
costs of preparing, filing and prosecuting patent applications, maintaining and enforcing
our intellectual property and proprietary rights and defending intellectual property-related claims
in the United States and internationally; |
| | |
| ● | the
number and characteristics of product candidates that we develop or may in-license; |
| | |
| ● | our
ability to establish and maintain collaborations on favorable terms, if at all; |
| | |
| ● | the
achievement of milestones or occurrence of other developments that trigger payments under
any collaboration agreements we enter into; |
| | |
| ● | the
outcome, timing and cost of meeting regulatory requirements established by the FDA, the European
Medical Agency (the “EMA”) and other comparable foreign regulatory authorities; |
| | |
| ● | the
cost and timing of completion of commercial-scale outsourced manufacturing activities; |
| | |
| ● | the
cost of establishing sales, marketing and distribution capabilities for any product candidates
for which we may receive regulatory approval in regions where we choose to commercialize
our products on our own; and |
| | |
| ● | the
costs of operating as a public company. |
Conducting
preclinical testing and clinical trials is a time-consuming, expensive and uncertain process that takes years to complete, and we
may never generate the necessary data or results required to obtain marketing approval and achieve product sales. In addition, even if
we successfully develop product candidates and those are approved, we may not achieve commercial success. Our commercial revenues, if
any, will be derived from sales of products that we do not expect to be commercially available for several years, if at all. Accordingly,
we will need to continue to rely on additional financing to achieve our business objectives.
Any
additional fundraising efforts may divert our management from our day-to-day activities, which may adversely affect our ability
to develop and commercialize product candidates. We cannot be certain that additional funding will be available on acceptable terms,
or at all. We have no committed source of additional capital and, if we are unable to raise additional capital in sufficient amounts
or on terms acceptable to us, we may have to significantly delay, scale back or discontinue the development or commercialization of product
candidates or other research and development initiatives. Our license agreements and any future collaboration agreements may also be
terminated if we are unable to meet the payment or other obligations under the agreements. We could be required to seek collaborators
for product candidates at an earlier stage than otherwise would be desirable or on terms that are less favorable than might otherwise
be available or relinquish or license on unfavorable terms our rights to product candidates in markets where we otherwise would seek
to pursue development or commercialization ourselves.
In
addition, as AMHC was a shell company prior to the completion of the Business Combination, we are currently ineligible to new short form
registration statements on Form S-3 and will not be eligible to file such a registration statement until, among other things, at least
12 calendar months have lapsed since September 29, 2021, the date we filed a Current Report on Form 8-K disclosing that we ceased to
be a shell company. Our inability to use Form S-3 may significantly impair our ability to raise necessary capital to run our operations
and progress our product development programs. If we seek to access the capital markets through a registered offering during the period
of time that we are unable to use Form S-3, we may be required to publicly disclose the proposed offering and the material terms thereof
before the offering commences, we may experience delays in the offering process due to SEC review of a Form S-1 registration statement
and we may incur increased offering and transaction costs and other considerations. Disclosing a public offering prior to the formal
commencement of an offering may result in downward pressure on our stock price. If we are unable to raise capital through a registered
offering, we would be required to conduct our equity financing transactions on a private placement basis, which may be subject to pricing,
size and other limitations imposed under the rules of The Nasdaq Stock Market LLC, or seek other sources of capital.
As a result of our recurring losses from operations and recurring negative
cash flows from operations, our management concluded that there is a substantial doubt about our ability to maintain liquidity sufficient
to operate our business effectively, which raise substantial doubt about our ability to continue as a going concern. See the risk factor
below titled, “As a result of our history of losses and negative cash flows from operations, our consolidated financial statements
contain a statement regarding a substantial doubt about our ability to continue as a going concern.” Based on our current operating
plan, we will need to raise additional financing to continue our products’ development for the foreseeable future, and until we
become profitable. If we are unable to obtain funding when and as needed on a timely basis, we may be required to significantly curtail,
delay or discontinue one or more of our research or development programs or the commercialization of any product candidate, or be unable
to expand our operations or otherwise capitalize on our business opportunities, as desired, which could materially affect our business,
financial condition and results of operations. Any of the above events could significantly harm our business, prospects, financial condition
and results of operations and cause the price of our common stock to decline.
We
have a limited operating history and no history of commercializing pharmaceutical products, which may make it difficult to evaluate the
prospects for our future viability.
We
are a clinical stage company. Old Jasper was founded and commenced operations in March 2018. Our operations to date have been limited
to organizing and staffing our company, business planning, raising capital, acquiring and developing our technology, identifying potential
product candidates and undertaking preclinical studies and clinical trials. Although we have initiated clinical trials for JSP191, we
have not yet demonstrated an ability to successfully complete clinical trials of our product candidates; obtained marketing approvals;
manufactured a commercial-scale medicine or therapy, or arranged for a third party to do so on our behalf; or conducted sales and marketing
activities necessary for successful commercialization. Typically, it takes about 10 to 15 years to develop a new
medicine from the time it is discovered to when it is available for treating patients. Consequently, any predictions we make about our
future success or viability may not be as accurate as they could be if we had a longer operating history.
In
addition, as a young business, we may encounter unforeseen expenses, difficulties, complications, delays and other known and unknown
factors. We will need to transition at some point from a company with a research and development focus to a company capable of supporting
commercial activities. We may not be successful in such a transition.
We
have never generated revenue from product sales and may never be profitable.
Our
ability to generate revenue from product sales and achieve profitability depends on our ability, alone or with collaborators, to successfully
complete the development of, and obtain the regulatory approvals necessary to commercialize, product candidates. We do not anticipate
generating revenues from product sales for the next several years, if ever. Our ability to generate future revenue from product
sales depends heavily on our, or our future collaborators’, ability to successfully:
| ● | identify
product candidates and complete research and preclinical and clinical development of any
product candidates we may identify; |
| | |
| ● | seek
and obtain regulatory and marketing approvals for any product candidates for which we complete
clinical trials; |
| | |
| ● | launch
and commercialize any product candidates for which we obtain regulatory and marketing approval
by establishing a sales force, marketing and distribution infrastructure or, alternatively,
collaborating with a commercialization partner; |
| | |
| ● | qualify
for coverage and adequate reimbursement by government and third-party payors for any
product candidates for which we obtain regulatory and marketing approval; |
| ● | develop,
maintain, and enhance a sustainable, scalable, reproducible, and transferable manufacturing
process for the product candidates we may develop; |
| ● | establish
and maintain supply and manufacturing relationships with third parties that can provide adequate,
in both amount and quality, products and services to support clinical development and the
market demand for any product candidates for which we obtain regulatory and marketing approval; |
| ● | obtain
market acceptance of product candidates as viable treatment options; |
| ● | address
competing technological and market developments; |
| ● | implement
internal systems and infrastructure, as needed; |
| ● | negotiate
favorable terms in any collaboration, licensing or other arrangements into which we may enter,
and perform our obligations in such arrangements; |
| ● | maintain,
protect, enforce, defend and expand our portfolio of intellectual property rights, including
patents, trade secrets and know-how, in the United States and internationally; |
| ● | avoid
and defend against third-party interference, infringement and other intellectual property
claims in the United States and internationally; and |
| ● | attract,
hire and retain qualified personnel. |
Even
if one or more of the product candidates we develop are approved for commercial sale, we anticipate incurring significant costs associated
with commercializing any approved product candidate. Our expenses could increase beyond expectations if we are required by the FDA, the
EMA or other regulatory authorities to perform clinical and other studies in addition to those that we currently anticipate.
Many
of the factors listed above are beyond our control, and could cause us to experience significant delays or prevent us from completing
the development of our product candidates, obtaining regulatory approvals or commercializing our product candidates. Even if we do achieve
profitability, we may not be able to sustain or increase profitability on a quarterly or annual basis. A failure to become or remain
profitable could result in a decline in the value of our company and could also cause you to lose all or part of your investment.
As
a result of our history of losses and negative cash flows from operations, our consolidated financial statements contain a statement
regarding a substantial doubt about our ability to continue as a going concern.
Our
history of operating losses and negative cash flows from operations combined with our anticipated use of cash to fund operations raises
substantial doubt about our ability to continue as a going concern beyond the 12-month period from the issuance date of our
consolidated financial statements included in Part II, Item 8 of this Annual Report on Form 10-K. Based on our current operating plan,
we will need to raise additional financing to continue our products’ development for the foreseeable future, and until we become
profitable. Our future viability as an ongoing business is dependent on our ability to generate cash from our operating activities or
to raise additional capital to finance our operations.
The
perception that we might be unable to continue as a going concern may also make it more difficult to obtain financing for the continuation
of our operations on terms that are favorable to us, or at all, and could result in the loss of confidence by investors and employees.
Our consolidated financial statements do not include any adjustments that might result from the outcome of this uncertainty. If we are
unable to continue as a going concern, we may have to liquidate our assets and may receive less than the value at which those assets
are carried on our consolidated financial statements, and it is likely that our investors will lose all or a part of their investment.
Our
ability to utilize our net operating loss carryforwards and certain other tax attributes to offset taxable income or taxes may be limited.
As of December 31, 2021, we had net operating loss carryforwards
for federal income tax purposes of $53.1 million that can be carried forward indefinitely. As of December 31, 2021, we
had net operating loss carryforwards for state income tax purposes of $45.4 million that begin to expire in 2038. Portions
of these net operating loss carryforwards could expire unused and be unavailable to offset future income tax liabilities. Under the legislation
enacted in 2017, informally titled the Tax Cuts and Jobs Act (the “Tax Act”), as modified by the Coronavirus Aid, Relief,
and Economic Security Act (the “CARES Act”), U.S. federal net operating losses incurred in taxable years beginning
after December 31, 2017 may be carried forward indefinitely, but the deductibility of such federal net operating losses in taxable years
beginning after December 31, 2020 is limited. It is uncertain how various states will respond to the Tax Act and the CARES Act. For
state income tax purposes, there may be periods during which the use of net operating loss carryforwards is suspended or otherwise limited,
which could accelerate or permanently increase state taxes owed. In addition, under Sections 382 and 383 of the Internal Revenue
Code of 1986, as amended (the “Code”), and corresponding provisions of state law, if a corporation undergoes an “ownership
change,” which is generally defined as a greater than 50% change, by value, in its equity ownership over a three-year period,
the corporation’s ability to use its pre-change net operating loss carryforwards and other pre-change tax attributes to offset its
post-change income or taxes may be limited. Our existing net operating loss carryforwards may be subject to limitations arising out of
previous ownership changes and we may be limited as to the amount that can be utilized each year as a result of such previous ownership
changes, including the Business Combination and related transactions. In addition, future changes in our stock ownership, including future
offerings, as well as other changes that may be outside of our control, could result in additional ownership changes. We have completed
a Section 382 analysis covering taxable periods from its inception through the year ended December 31, 2021. We experienced
an ownership change on November 21, 2019 for both federal and California tax purposes related to its Series A redeemable convertible
preferred stock financing. Any net operating loss generated for taxable periods in 2018 and through November 21, 2019 in excess of
$2.87 million will be permanently limited for California tax purposes. We reduced our California net operating loss deferred tax
assets balance by the permanently limited amount of $0.6 million. There would be no permanent loss of federal net operating loss
based on the limits. We experienced an additional ownership change on September 24, 2021. However, we do not expect there are additional
tax attributes that will expire unused before the expiration periods. There is a full valuation allowance for net deferred tax assets,
including net operating loss carryforwards for the year ended December 31, 2021.
Our
business could be adversely affected by the effects of health pandemics or epidemics, including the current COVID-19 pandemic and future
outbreaks of the disease, in regions where we or third parties on which we rely have concentrations of clinical trial sites or other
business operations.
Our
business could be adversely affected by the effects of health pandemics or epidemics, including the current COVID-19 pandemic and future
outbreaks of the disease, including any variants thereof. For example, enrollment in clinical trials may be delayed. Although we have
reopened our offices and some employees have transitioned back to working on site, there is a lack of uniformity of restrictions and
requirements among our clinical trial sites, and future shelter-in-place or similar types of restrictions could be imposed. We are subject
to risk of outbreaks at our facilities, and potential exposure to employee claims regarding workplace safety, and unanticipated shutdowns
or quarantines could be imposed in the future, which would disrupt our operations. This uncertainty and the evolving nature of policies
and restrictions may negatively impact productivity, disrupt our business and further delay clinical programs and timelines, the magnitude
of which will depend, in part, on the length and severity of the restrictions and other limitations on our ability to conduct our business
in the ordinary course, which could negatively impact our business, operating results and financial condition.
The
spread of COVID-19, which has caused a broad impact globally, may affect us economically. While the potential economic impact brought
by, and the duration of, the COVID-19 pandemic may be difficult to assess or predict, it has resulted in significant disruption of global
financial markets. This disruption, if sustained or recurrent, could make it more difficult for us to access capital, which could in
the future negatively affect our liquidity. In addition, a recession or market correction resulting from the spread of COVID-19 or the
global impacts thereof could materially affect our business and the value of our common stock. The global COVID-19 pandemic continues
to evolve, and its ultimate impact or that of any similar health pandemic or epidemic is highly uncertain. We do not yet know the full
extent of potential delays or impacts on our business, our planned and ongoing clinical trials, the hospitals and healthcare systems
or the global economy as a whole. These effects could have an adverse impact on our operations, and we will continue to monitor the COVID-19
situation closely.
Business disruptions caused by natural or man-made disasters, acts
of war or other hostilities could seriously harm our future revenues and financial condition and increase our costs and expenses generally.
Our corporate headquarters are located in the San Francisco Bay Area,
a region known for seismic activity. Our suppliers may also experience a disruption in their business as a result of natural or man-made
disasters. A significant natural or man-made disaster, such as an earthquake, prolonged or repeated power outage, hurricane, flood, fire,
drought or other extreme weather events and changing weather patterns, which are increasing in frequency due to the impacts of climate
change, could severely damage or destroy our headquarters or facilities or the facilities of our manufacturers or suppliers, which could
have a material and adverse effect on our business, financial condition and results of operations. In addition, terrorist acts, acts of
war or the outbreak of hostilities against the U.S. or other countries globally, could cause damage or disruption to us, our employees,
facilities, partners and suppliers, which could have a material adverse effect on our business, financial condition and results of operations.
Risks
Related to Discovery, Development, Manufacturing and Commercialization
We
are substantially dependent on the success of our most advanced product candidate, JSP191. If we are unable to complete development of,
obtain approval for and commercialize our product candidates, including JSP191, in a timely manner or at all, our business will be harmed.
Our
future success is dependent on our ability to timely advance and complete clinical trials, obtain marketing approval for and successfully
commercialize our product candidates. We are not permitted to market or promote JSP191 or any other product candidate before we receive
marketing approval from the FDA and comparable foreign regulatory authorities, and we may never receive such marketing approvals.
The
success of our product candidates will depend on several factors, including the following:
| ● | the
acceptance of individual investigational review boards (“IRBs”) and scientific
review committees at each clinical trial site as to the adequacy of the preclinical data
package to support clinical development of JSP191 and their overall general agreement with
the use of JSP191 in the intended patient population in the intended manner; |
| ● | the
willingness of clinical investigators to place patients in the clinical trials, and the willingness
of patients to enroll in a clinical trial studying a first-in-human cell therapy; |
| ● | the
initiation and successful patient enrollment and completion of additional clinical trials
of JSP191 on a timely basis; |
| ● | the
frequency and severity of adverse events in the clinical trials; |
| ● | the
successful and timely completion of our ongoing Phase 1/2 clinical trial of JSP191 for the
treatment of SCID and the ongoing Phase 1 clinical trial of JSP191 for AML or MDS; |
| ● | maintaining
and establishing relationships with contract research organizations (“CROs”)
and clinical sites for the clinical development of JSP191 both in the United States and internationally; |
| ● | successful
completion of toxicology studies, biodistribution studies and minimally efficacious dose
studies in animals, where applicable; |
| ● | successful
completion of clinical trials, under the FDA’s current Good Clinical Practices (“cGCPs”)
and the FDA’s current Good Laboratory Practices; |
| ● | effective
investigational new drug (“IND”) applications or Clinical Trial Authorizations
that allow commencement of our planned clinical trials or future clinical trials for our
product candidates; |
| ● | the
results of clinical trials conducted by third parties in hematopoietic stem cell transplant
(“HSCT”) if such trials result in changes to the standard of care for HSCT or
otherwise cause us to change our clinical trial protocols; |
| ● | the
efficacy, safety and tolerability profiles that are satisfactory to the FDA, EMA or any comparable
foreign regulatory authority for marketing approval; |
| ● | the
timely receipt of marketing approvals for our product candidates from applicable regulatory
authorities; |
| ● | the
extent of any required post-marketing approval commitments to applicable regulatory authorities; |
| ● | the
maintenance of existing or the establishment of new supply arrangements with third-party
suppliers and manufacturers for clinical development of JSP191; |
| ● | the
maintenance of existing, or the establishment of new, scaled production arrangements with
third-party manufacturers to obtain finished products that are appropriate for commercial
sale of JSP191, if it is approved; |
| ● | obtaining
and maintaining patent protection, trade secret protection and regulatory exclusivity, both
in the United States and internationally; |
| ● | a
continued acceptable safety profile following any marketing approval; |
| ● | commercial
acceptance by patients, the medical community and third-party payors; |
| ● | our
ability to obtain coverage and adequate reimbursement from third-party payors for our products,
and patients’ willingness to pay out-of-pocket in the absence of such coverage and
adequate reimbursement; and |
| ● | our
ability to compete with other treatments. |
We
do not have complete control over many of these factors, including certain aspects of clinical development and the regulatory submission
process, potential threats to our intellectual property rights and the manufacturing, marketing, distribution and sales efforts of any
future collaborator. If we are not successful with respect to one or more of these factors in a timely manner or at all, we could experience
significant delays or an inability to successfully commercialize JSP191, which would materially harm our business. If we do not receive
marketing approvals for JSP191, we may not be able to continue our operations.
We
may not be successful in our efforts to identify, develop and commercialize additional product candidates. If these efforts are
unsuccessful, we may never become a commercial stage company or generate any revenues.
The
success of our business depends primarily upon our ability to identify, develop and commercialize additional product candidates based
on, or complementary with, our technology platform. While we are currently conducting a Phase 1/2 clinical trial of JSP191 as a
conditioning agent prior to allogenic transplant for SCID patients, a Phase 1 clinical trial of JSP191 as a conditioning agent prior
to allogenic transplant for patients with AML or MDS, and are planning a Phase 1 clinical trial of JSP191 as a conditioning agent
prior to allogenic transplant, all of our other product development programs, including our eHSC program, are still in the research or
preclinical stage of development. Our research programs may fail to identify additional product candidates for clinical development for
a number of reasons. Our research methodology may be unsuccessful in identifying potential product candidates, our potential product
candidates may be shown to have harmful side effects in preclinical in vitro experiments or animal model studies, they may not show promising
signals of efficacy in such experiments or studies or they may have other characteristics that may make the product candidates impractical
to manufacture, unmarketable or unlikely to receive marketing approval. The historical failure rate for product candidates is high due
to risks relating to safety, efficacy, clinical execution, changing standards of medical care and other unpredictable variables. In addition,
although we believe our technology platform will position us to rapidly expand our portfolio of product candidates beyond our current
product candidates, our ability to expand our portfolio may never materialize.
If
any of these events occur, we may be forced to abandon our research or development efforts for a program or programs, which would have
a material adverse effect on our business, financial condition, results of operations and prospects. Research programs to identify new
product candidates require substantial technical, financial and human resources. We may focus our efforts and resources on potential
programs or product candidates that ultimately prove to be unsuccessful, which would be costly and time-consuming.
eHSCs
are a novel technology that is not yet clinically validated for human use. The approaches we are taking to create eHSCs are unproven
and may never lead to marketable products.
We
are developing eHSCs for transplant into the human body. Although there have been significant advances in the field of use of RNA or
DNA to edit cells ex vivo prior to transplant in recent years, these technologies have only more recently been applied to HSCs,
and our approach is new and unproven. The scientific evidence to support the feasibility of developing eHSCs is both preliminary and
limited. Successful development of eHSCs by us will require solving a number of challenges, including:
| ● | obtaining
regulatory authorization from the FDA and other regulatory authorities; |
| ● | identifying
appropriate molecular or genetic targets for modification within HSCs; |
| ● | developing
and deploying consistent and reliable processes for procuring cells from consenting third-party
donors, isolating HSCs from such donor cells, modifying target molecules within such HSCs,
storing and transporting the resulting eHSCs for therapeutic use and finally infusing these
eHSCs into patients; |
| ● | utilizing
these eHSC product candidates in combination or in sequence with companion therapeutics,
which may increase the risk of adverse side effects; |
| ● | avoiding
potential complications of eHSC transplants, including failure to engraft, rejection by host
or lack of functionality, any of which could result in serious side effects or death; |
| ● | educating
medical personnel regarding the potential side effect profile of our product candidates,
particularly those that may be unique to our eHSCs; |
| ● | understanding
and addressing variability in the quality of a donor’s cells, which could ultimately
affect our ability to manufacture product in a reliable and consistent manner; |
| ● | developing
processes for the safe administration of eHSC products, including long-term follow-up and
registries, for all patients who receive these product candidates; |
| ● | relying
on third parties to find suitable healthy donors; |
| ● | manufacturing
product candidates to our specifications and in a timely manner to support our clinical trials
and, if approved, commercialization; |
| ● | sourcing
clinical and, if approved by applicable regulatory authorities, commercial supplies for the
materials used to manufacture and process product candidates; |
| ● | developing
a manufacturing process and distribution network that can provide a stable supply with a
cost of goods that allows for an attractive return on investment; and |
| ● | establishing
sales and marketing capabilities ahead of and after obtaining any regulatory approval to
gain market acceptance, and obtaining coverage, adequate reimbursement and pricing by third-party
payors and governmental healthcare programs. |
We
may decide to alter or abandon our initial eHSC programs as new data become available and we gain experience in developing eHSCs. We
cannot be sure that our programs will yield satisfactory products that are safe and effective, scalable or profitable in our initial
indication or any other indication we pursue.
Moreover,
actual or perceived safety issues, including as a result of adverse developments in our eHSC programs or in genome engineering programs
undertaken by third parties or of the adoption of novel approaches to treatment, may adversely influence the willingness of subjects
to participate in our clinical trials, or, if one of our product candidates is approved by applicable regulatory authorities, of physicians
to subscribe to the novel treatment mechanics or of patients to provide consent to receive a novel treatment despite its regulatory approval.
The FDA or other applicable regulatory authorities may require specific post-market studies or additional information that communicates
the benefits or risks of our products. New data may reveal new risks of our product candidates at any time prior to or after regulatory
approval.
If
any of our product candidates cause serious adverse events, undesirable side effects or unexpected characteristics, such events, side
effects or characteristics could delay or prevent regulatory approval of the product candidate, limit our commercial potential or result
in significant negative consequences following any potential marketing approval.
Undesirable
side effects or adverse events caused by JSP191 and our other product candidates, and our eHSCs or other cell-based companion therapeutics
we may develop, could cause us or regulatory authorities to interrupt, delay or halt clinical trials and could result in a more restrictive
label or the delay or denial of regulatory approval by the FDA or comparable foreign regulatory authorities. Results of our clinical
trials could reveal a high and unacceptable severity and prevalence of side effects or unexpected characteristics. Treatment-related
side effects could also affect patient recruitment or the ability of enrolled patients to complete the trials or result in potential
product liability claims.
There
have been no clinical trials of eHSCs. In the genetic medicine field, there have been several significant adverse events from genetically
engineered treatments in the past, including reported cases of leukemia and death. There can be no assurance that our eHSCs will not
cause undesirable side effects, as improper modification of a patient’s DNA could lead to lymphoma, leukemia or other cancers,
or other aberrantly functioning cells.
A
significant risk in any genetically engineered product candidate is that “off-target” gene alterations may occur, which could
cause serious adverse events, undesirable side effects or unexpected characteristics. Although we and others have demonstrated the ability
to improve the specificity of gene alterations in a laboratory setting, we cannot be certain that off-target alterations will not occur
in any of our planned or future clinical trials, and the lack of observed side effects in preclinical studies does not guarantee that
such side effects will not occur in human clinical trials.
If
any product candidates we develop are associated with serious adverse events, undesirable side effects or unexpected characteristics,
we may need to abandon their development or limit development to certain uses or subpopulations in which the serious adverse events,
undesirable side effects or other characteristics are less prevalent, less severe or more acceptable from a risk-benefit perspective,
any of which would have a material adverse effect on our business, financial condition, results of operations, and prospects. Many product
candidates that initially showed promise in early stage testing have later been found to cause side effects that prevented further clinical
development of the product candidates.
Results
of preclinical studies and early clinical trials may not be predictive of results of future clinical trials, and such results do not
guarantee approval of a product candidate by regulatory authorities. In addition, our clinical trials to date have been limited in scope,
and results received to date may not be replicated in expanded or additional future clinical trials.
The
outcome of preclinical studies and early clinical trials may not be predictive of the success of later clinical trials, and interim results
of clinical trials do not necessarily predict success in the results of completed clinical trials. There can be no assurance that any
of our current or future preclinical and clinical trials will ultimately be successful or support further preclinical or clinical development
of any of our product candidates. Many companies in the pharmaceutical and biotechnology industries have suffered significant setbacks
in late-stage clinical trials after achieving positive results in earlier development, and we could face similar setbacks. The design
of a clinical trial can determine whether its results will support approval of a product, and flaws in the design of a clinical trial
may not become apparent until the clinical trial is well advanced. Many companies that believed their product candidates performed satisfactorily
in preclinical studies and clinical trials have nonetheless failed to obtain regulatory approval for their product candidates. In addition,
preclinical and clinical data are often susceptible to varying interpretations and analyses, which may delay, limit or prevent regulatory
approval. In addition, regulatory delays or rejections may be encountered as a result of many factors, including changes in regulatory
policy during the period of product development. Any such adverse events may cause us to delay, limit or terminate planned clinical trials,
any of which would have a material adverse effect on our business, financial condition, results of operations and prospects.
In
some instances, there can be significant variability in safety or efficacy results between different clinical trials of the same product
candidate due to numerous factors, including changes in trial procedures set forth in protocols, differences in the size and type of
the patient populations, changes in and adherence to the dosing regimen and other clinical trial procedures and the rate of dropout among
clinical trial participants. If we fail to receive positive results in clinical trials of our product candidates, the development timeline
and regulatory approval and commercialization prospects for our most advanced product candidate, and, correspondingly, our business and
financial prospects would be negatively impacted.
If
we experience delays or difficulties in the enrollment of patients in clinical trials, the cost of developing product candidates could
increase and our receipt of necessary regulatory approvals could be delayed or prevented.
Patient
enrollment is a significant factor in the timing of clinical trials. The timing of our clinical trials depends, in part, on the speed
at which we can recruit patients to participate in our trials. We or our collaborators may not be able to continue clinical trials for
JSP191 or any other product candidates we identify or develop if we are unable to locate and enroll a sufficient number of eligible patients
to participate in these trials as required by the FDA, the EMA or other analogous regulatory authorities outside the United States,
or as needed to provide appropriate statistical power for a given trial. Patients may be unwilling to participate in our clinical trials
because of negative publicity from adverse events related to the biotechnology, gene therapy or genome engineering fields, competitive
clinical trials for similar patient populations, clinical trials in competing products or for other reasons. As a result, the timeline
for recruiting patients, conducting trials and obtaining regulatory approval of product candidates may be delayed.
Patient
enrollment is also affected by other factors, including:
| ● | severity
of the disease under investigation; |
| ● | size
of the patient population and process for identifying patients; |
| ● | design
of the trial protocol; |
| ● | availability
and efficacy of approved medications for the disease under investigation; |
| ● | availability
of genetic testing for potential patients; |
| ● | ability
to obtain and maintain patient informed consent; |
| ● | risk
that enrolled patients will drop out before completion of the trial; |
| ● | eligibility
and exclusion criteria for the trial in question; |
| ● | perceived
risks and benefits of the product candidate under trial; |
| ● | perceived
risks and benefits of genome engineering as a treatment approach; |
| ● | perceived
risks and benefits of the companion therapeutics that may be administered in combination
or in sequence with JSP191; |
| ● | efforts
to facilitate timely enrollment in clinical trials; |
| ● | potential
disruptions caused by the COVID-19 pandemic, including difficulties in initiating clinical
sites, enrolling and retaining participants, diversion of healthcare resources away from
clinical trials, travel or quarantine policies that may be implemented, and other factors; |
| ● | patient
referral practices of physicians; |
| ● | ability
to monitor patients adequately during and after treatment; |
| ● | proximity
and availability of clinical trial sites for prospective patients, especially for those conditions
that have small patient pools; |
| ● | the
requirement for HSCT to be performed in centers that specialize in this procedure; and |
| ● | changes
to diagnostic technologies, methodologies or criteria used to identify HSCT patients at high
risk for relapse. |
In
addition, our clinical trials will compete with other clinical trials for product candidates that are in the same therapeutic areas as
our product candidates, and this competition will reduce the number and types of patients available to us because some patients who have
opted to enroll in our trials may instead opt to enroll in a trial being conducted by a competitor. We may conduct some of our clinical
trials at the same clinical trial sites that some of our competitors use, which will reduce the number of patients who are available
for our clinical trials at such clinical trial sites.
Enrollment
delays in our clinical trials may result in increased development costs for JSP191 or any other product candidates we may develop, which
would cause the value of our company to decline and limit our ability to obtain additional financing. If we or our collaborators have
difficulty enrolling a sufficient number of patients to conduct our clinical trials as planned, we may need to delay, limit or terminate
ongoing or planned clinical trials, any of which would have an adverse effect on our business, financial condition, results of operations
and prospects.
We
have never obtained regulatory approval for a drug, may never receive regulatory approval for any of our product candidates, and may
therefore never generate revenues from product sales.
As
a company, we have never obtained regulatory approval for, or commercialized, a drug. It is possible that the FDA may refuse to accept
any or all future product candidates for substantive review or may conclude after review of our data that our application is insufficient
to obtain regulatory approval for any current or future product candidates. If the FDA does not approve any future product candidates,
it may require that we conduct additional costly clinical, preclinical or manufacturing validation studies before the FDA will reconsider
one or more of our applications. Depending on the extent of these or any other FDA-required studies, approval of any product candidates
or other application that we submit may be significantly delayed, possibly for several years, or may require us to expend more resources
than we have available. Any failure or delay in obtaining regulatory approvals would prevent us from commercializing JSP191 or any other
product candidate, generating revenues and achieving and obtaining or sustaining profitability. It is also possible that additional studies,
if performed and completed, may not be considered sufficient by the FDA to approve any new drug application or other application we submit.
If any of these outcomes occur, we may be forced to abandon the development of our product candidates, which would materially adversely
affect our business and could potentially cause us to cease operations. We face similar risks for our applications in foreign jurisdictions.
Our
commercial success depends upon attaining significant market acceptance of our product candidates, if approved, among physicians, patients,
healthcare payers and operators of major clinics, and we may not be successful in attaining such market acceptance.
Even
with the requisite approvals from the FDA in the U.S., the EMA in the European Union and other regulatory authorities internationally,
the commercial success of our product candidates will depend, in part, upon the degree of market acceptance by physicians, patients,
third-party payors and others in the medical community. Any product that we commercialize may not gain acceptance by physicians, patients,
health care payors and others in the medical community. If these products do not achieve an adequate level of acceptance, we may not
generate significant product revenue and may not become profitable. Efforts to educate the medical community and third-party payors on
the benefits of our product candidates may require significant resources, including our management’s time and financial resources,
and may not be successful. Ethical, social and legal concerns about genetic medicines generally and genome engineering technologies specifically
could result in additional regulations restricting or prohibiting the marketing of our product candidates. Even if any product candidate
we develop receives marketing approval, it may nonetheless fail to gain sufficient market acceptance by physicians, patients, healthcare
payors and others in the medical community. The degree of market acceptance of any product candidate we develop, if approved for commercial
sale, will depend on a number of factors, including:
|
● |
the efficacy and safety of
such product candidate as demonstrated in clinical trials; |
|
● |
the efficacy and safety of
other products that are used in combination or in sequence with our product candidates; |
|
● |
the potential and perceived
advantages of our product candidates compared to alternative treatments; |
|
● |
the limitation to our targeted
patient population and limitations or warnings contained in approved labeling by the FDA or other regulatory authorities; |
|
● |
the ability to offer our products
for sale at competitive prices; |
|
● |
convenience and ease of administration
compared to alternative treatments; |
|
● |
the clinical indications for
which the product candidate is approved by the FDA, the EMA or other regulatory agencies; |
|
● |
public attitudes regarding
genetic medicine generally and genome engineering technologies specifically; |
|
● |
the willingness of the target
patient population to try novel biologics and of physicians to prescribe these treatments, as well as their willingness to accept
an intervention that involves the alteration of the patient’s gene; |
|
● |
product labeling or product
insert requirements of the FDA, the EMA or other regulatory authorities, including any limitations or warnings contained in a product’s
approved labeling; |
|
● |
relative convenience and ease
of administration; |
|
● |
the strength of marketing and
distribution support; |
|
● |
availability of third-party
coverage and sufficiency of reimbursement; and |
|
● |
the prevalence and severity
of any side effects. |
Even
if a product candidate is approved, such product may not achieve an adequate level of acceptance, we may not generate significant product
revenues, and we may not become profitable.
If
we are unable to establish effective marketing and sales capabilities or enter into agreements with third parties to market and sell
our product candidates, if approved, we may not be able to effectively market and sell our product candidates, if approved, or generate
product revenues.
We
have limited marketing capabilities and limited experience in the sale, marketing or distribution of pharmaceutical products. In addition,
we do not have a large sales, promotion and marketing budget. As a result of our limited marketing capabilities, to achieve commercial
success for any approved product for which we retain sales and marketing responsibilities, we must either develop a sales and marketing
organization or outsource these functions to third parties. In the future, we may choose to build a focused sales, marketing and commercial
support infrastructure to sell, or participate in sales activities with our collaborators for, some of our product candidates if and
when they are approved.
Factors
that may inhibit our efforts to commercialize our product candidates on our own include:
|
● |
our inability to recruit and
retain adequate numbers of effective sales, marketing, reimbursement, customer service, medical affairs and other support personnel; |
|
● |
the inability of sales personnel
to obtain access to physicians or educate adequate numbers of physicians on the benefits of prescribing any future products; |
|
● |
the inability of reimbursement
professionals to negotiate arrangements for formulary access, reimbursement and other acceptance by payors; |
|
● |
restricted or closed distribution
channels that make it difficult to distribute our product candidates to segments of the patient population; |
|
● |
the lack of complementary products
to be offered by sales personnel, which may put us at a competitive disadvantage relative to companies with more extensive product
lines; and |
|
● |
unforeseen costs and expenses
associated with creating an independent commercialization organization. |
We
may not be successful in entering into arrangements with third parties to commercialize our product candidates or may be unable to do
so on terms that are favorable to us. We may have little control over such third parties, and any of them may fail to devote the necessary
resources and attention to sell and market our products effectively. If we do not establish commercialization capabilities successfully,
either on our own or in collaboration with third parties, we will not be successful in commercializing our product candidates.
We
face significant competition in an environment of rapid technological change, and there is a possibility that our competitors may achieve
regulatory approval before us or develop therapies that are safer or more advanced or effective than ours, which may harm our financial
condition and our ability to successfully market or commercialize our product candidates.
The
development and commercialization of new drug and biologic products is highly competitive. Moreover, the genome engineering and oncology
fields are characterized by rapidly changing technologies, significant competition and a strong emphasis on intellectual property. We
will face competition with respect to JSP191 and any other product candidates that we develop or commercialize in the future from major
pharmaceutical companies, specialty pharmaceutical companies and biotechnology companies worldwide. Potential competitors also include
academic institutions, government agencies and other public and private research organizations that conduct research, seek patent protection
and establish collaborative arrangements for research, development, manufacturing and commercialization.
There
are a number of large pharmaceutical and biotechnology companies that currently market and sell products or are pursuing the development
of products for the treatment of the disease indications for which we have product candidates and research programs. Some of these competitive
products and therapies are based on scientific approaches that are the same as or similar to our approach, and others are based on entirely
different approaches. Any product candidates that we successfully develop and commercialize will compete with existing therapies and
new therapies that may become available in the future that are approved to treat the same diseases for which we may obtain approval for
our product candidates. This may include other types of therapies, such as small molecule, antibody and/or protein therapies.
Many
of our current or potential competitors, either alone or with their collaboration partners, may have significantly greater financial
resources and expertise in research and development, manufacturing, preclinical testing, conducting clinical trials, obtaining regulatory
approvals and marketing approved products than we do. Mergers and acquisitions in the pharmaceutical, biotechnology and gene therapy
industries may result in even more resources being concentrated among a smaller number of our competitors. Smaller or early-stage companies
may also prove to be significant competitors, particularly through collaborative arrangements with large and established companies. These
competitors also compete with us in recruiting and retaining qualified scientific and management personnel and establishing clinical
trial sites and patient registration for clinical trials, as well as in acquiring technologies complementary to, or necessary for, our
programs. Our commercial opportunity could be reduced or eliminated if our competitors develop and commercialize product candidates that
are safer, more effective, have fewer or less severe side effects, are more convenient or are less expensive than our product candidates
or that would render our product candidates obsolete or non-competitive. Our competitors also may obtain FDA or other regulatory approval
for their product candidates more rapidly than we may obtain approval for ours, which could result in our competitors establishing a
strong market position before we are able to enter the market. Additionally, technologies developed by our competitors may render our
product candidates uneconomical or obsolete, and we may not be successful in marketing any product candidates against competitors.
Competitors of JSP191 for our conditioning program
for CD-117, a receptor for stem cell factor (“SCF”) that is expressed on the surface of hematopoietic stem and progenitor
cells, include the following:
|
● |
Magenta Therapeutics, Inc.,
which is developing an Amanitin Anti-CD117 antibody drug conjugate and is in clinical development; |
|
● |
Gilead Sciences, Inc., which
is developing an antibody to CD117 that is not conjugated to any toxin and is used in combination with an antibody to CD47 and has
started initial Phase I clinical studies; |
|
● |
Actinium Pharmaceuticals, Inc.,
which is developing an antibody to CD45 that is linked to radioisotope iodine-131 and is in Phase III clinical studies; |
|
● |
Molecular Templates Inc., which
is developing an antibody to CD45 that is conjugated to engineered Shiga-toxin and is in preclinical development; and |
|
● |
Celldex Therapeutics, Inc.,
which is developing an antibody to inhibit tyrosine kinase KIT found in mast cells and is in Phase I/II clinical studies in
indications unrelated to conditioning. |
Competitors
for our engineered stem cell therapy program include the following:
|
● |
Gamida Cell Ltd., which is
developing an umbilical cord blood-derived cell product that uses a small molecule to inhibit differentiation and enhance functionality
of ex vivo-expanded HSCs; |
|
● |
ExCellThera Inc., which is
focused on ex vivo expansion of stem cells using a pyrimido-indole derivative small molecule; |
|
● |
Angiocrine Bioscience, Inc.,
which is expanding cord blood and gene-modified HSCs using an endothelial cell feeder layer; |
|
● |
Sana Biotechnology, Inc., which
is developing hypoimmune cells designed to evade rejection and enable persistence of allogeneic cells; |
|
● |
Vor Biopharma, Inc., which
is developing treatment-resistant marrow cells that enable CD33 targeted therapy; and |
|
● |
Ensoma Inc., which is developing
viral vectors for delivery of cell modification payload, in vivo. |
Adverse
public perception of genetic medicines, and genome engineering in particular, may negatively impact regulatory approval of, and/or demand
for, our potential products.
Some
of our eHSCs or other cell-based therapeutics we develop may be created by altering the human genome. The clinical and commercial success
of our potential products will depend in part on public understanding and acceptance of the use of genome engineering for the prevention
or treatment of human diseases. Public attitudes may be influenced by claims that genome engineering is unsafe, unethical or immoral,
and, consequently, our current or future product candidates may not gain the acceptance of the public or the medical community. Adverse
public attitudes may adversely impact our ability to enroll clinical trials. Moreover, our success will depend upon physicians prescribing,
and their patients being willing to receive, treatments that involve the use of product candidates in lieu of, or in addition to, existing
treatments with which they are already familiar and for which greater clinical data may be available.
In
addition, genome engineering technology is subject to public debate and heightened regulatory scrutiny due to ethical concerns relating
to the application of genome engineering technology to human embryos or the human germline. For example, in the United States, germline
alteration for clinical application has been expressly prohibited since enactment of a December 2015 FDA ban on such activity. Prohibitions
are also in place in the United Kingdom, across most of Europe, in China and many other countries around the world. In the United States,
the National Institutes of Health has announced that the agency would not fund any use of gene engineering technologies in human embryos,
noting that there are multiple existing legislative and regulatory prohibitions against such work, including the Dickey-Wicker Amendment,
which prohibits the use of appropriated funds for the creation of human embryos for research purposes or for research in which human
embryos are destroyed. Adverse events in our preclinical studies or clinical trials or those of our competitors or of academic researchers
utilizing genome engineering technologies, even if not ultimately attributable to product candidates we may identify and develop, and
the accompanying publicity could result in increased governmental regulation, unfavorable public perception, potential regulatory delays
in the testing or approval of potential product candidates we may identify and develop, stricter labeling requirements for those product
candidates that are approved and a decrease in demand for any such product candidates.
If
product liability lawsuits are brought against us, we may incur substantial liabilities and may be required to limit commercialization
of our product candidates.
We
face an inherent risk of product liability exposure related to the testing in human clinical trials of our product candidates and will
face an even greater risk if we commercially sell any products that we may develop. For example, we may be sued if our product candidates
cause, or are perceived to cause, injury or are found to be otherwise unsuitable during clinical trials, manufacturing, marketing or
sale. Any such product liability claims may include allegations of defects in manufacturing, defects in design, a failure to warn of
dangers inherent in the product, negligence, strict liability or a breach of warranties. Claims could also be asserted under state consumer
protection acts. If we cannot successfully defend ourselves against claims that our product candidates or products caused injuries, we
could incur substantial liabilities or be required to limit commercialization of our product candidates. Even a successful defense would
require significant financial and management resources. Regardless of merit or eventual outcome, liability claims may result in:
|
● |
the inability to commercialize
any products that we may develop; |
|
● |
decreased demand for our product
candidates or products that we may develop; |
|
● |
injury to our reputation and
significant negative media attention; |
|
● |
withdrawal of clinical trial
participants; |
|
● |
significant time and costs
to defend the related litigation; |
|
● |
substantial monetary awards
to trial participants or patients; and |
Although
we maintain product liability insurance coverage, it may not be adequate to cover all liabilities that we may incur. We anticipate that
we will need to increase our insurance coverage as we continue clinical trials and if we successfully commercializes any product. Insurance
coverage is increasingly expensive. We may not be able to maintain insurance coverage at a reasonable cost or in an amount adequate to
satisfy any liability that may arise.
Our
product candidates are complex and difficult to manufacture. We could experience delays in satisfying regulatory authorities or production
problems that result in delays in our development or commercialization programs, limit the supply of our product candidates, or otherwise
harm our business.
Our
product candidates require processing steps that are more complex than those required for most chemical and other biological pharmaceuticals.
Moreover, unlike chemical and other biological pharmaceuticals, the physical and chemical properties of a gene-engineered cell therapies
cannot be fully characterized. As a result, assays of the finished product candidate may not be sufficient to ensure that the product
candidate will perform in the intended manner. Problems with the manufacturing process, even minor deviations from the normal process,
could result in product defects or manufacturing failures that result in lot failures, product recalls, product liability claims, insufficient
inventory or potentially delay progression of our clinical trials. If we successfully develop product candidates, we may encounter problems
achieving adequate quantities and quality of clinical-grade materials that meet FDA, EMA or other comparable applicable foreign standards
or specifications with consistent and acceptable production yields and costs. In addition, our product candidates will require complicated
delivery modalities, such as electroporation, which will introduce additional complexities into the manufacturing process.
eHSCs
consist of engineered human cells, and the process of manufacturing such product candidates is complex, concentrated with a limited number
of suppliers, highly regulated and subject to numerous risks. Manufacturing such product candidates involves harvesting cells from a
donor or from the patient, altering the cells ex vivo using genome engineering technology, cryopreservation, storage and eventually
shipment and infusing the cell product into the patient’s body. Our manufacturing process will be susceptible to product loss or
failure, or product variation that may negatively impact patient outcomes, due to logistical issues associated with the collection of
starting material from the donor, shipping such material to the manufacturing site, shipping the final product back to the clinical trial
recipient, preparing the product for administration, infusing the patient with the product, manufacturing issues or different product
characteristics resulting from the differences in donor starting materials, variations between reagent lots, interruptions in the manufacturing
process, contamination, equipment or reagent failure, improper installation or operation of equipment, vendor or operator error, inconsistency
in cell growth and variability in product characteristics. our manufacturing process, like that of a number of other cell therapy companies,
is also characterized by limited numbers of suppliers, and in some cases sole source suppliers, with the manufacturing capabilities and
know-how to create or source the materials, such as donor marrow cells and electroporation machines, used in our cell manufacturing.
While we pursue multiple sources for the critical components of our manufacturing process, we may not be successful in securing these
additional sources at all or on a timely basis. If microbial, viral or other contaminations are discovered in our product candidates
or in any of the manufacturing facilities in which our product candidates or other materials are made, such manufacturing facilities
may need to be closed for an extended period of time to investigate and remedy the contamination.
In
addition, the FDA, the EMA and other regulatory authorities may require us to submit samples of any lot of approved product together
with the protocols showing the results of applicable tests at any time. Under some circumstances, the FDA, the EMA or other regulatory
authorities may require that we not distribute a lot until the agency authorizes its release. Slight deviations in the manufacturing
process, including those affecting quality attributes and stability, may result in unacceptable changes in the product that could result
in lot failures or product recalls. Lot failures or product recalls could cause us to delay clinical trials or product launches, which
could be costly to us and otherwise harm our business, financial condition, results of operations and prospects.
Some
of the raw materials that we anticipate will be required in our manufacturing process are derived from biologic sources. Such raw materials
are difficult to procure and may be subject to contamination or recall. A material shortage, contamination, recall or restriction on
the use of biologically derived substances in the manufacture of our product candidates could adversely impact or disrupt the commercial
manufacturing or the production of clinical material, which could materially harm our development timelines and our business, financial
condition, results of operations and prospects.
If
we or any contract research organizations, contract manufacturers or suppliers that we engage fail to comply with environmental, health
and safety laws and regulations, we could become subject to fines or penalties or incur costs that could have a material adverse effect
on the success of our business.
We
and any contract research organizations, contract manufacturers and suppliers we engage are subject to numerous federal, state and local
environmental, health and safety laws, regulations and permitting requirements, including those governing laboratory procedures; the
generation, handling, use, storage, treatment and disposal of hazardous and regulated materials and wastes; the emission and discharge
of hazardous materials into the ground, air and water; and employee health and safety. Our operations involve the use of hazardous and
flammable materials, including chemicals and biological and radioactive materials. Our operations also produce hazardous waste. We generally
contract with third parties for the disposal of these materials and wastes. Although we believe that our and such third parties’
procedures for handling, storing and disposing of these materials and waste comply with legally prescribed standards, we cannot eliminate
the risk of contamination or injury from these materials. In the event of contamination or injury resulting from our use of hazardous
materials, we could be held liable for any resulting damages, and any liability could exceed our resources. Under certain environmental
laws, we could be held responsible for costs relating to any contamination at our current or past facilities and at third-party facilities.
We also could incur significant costs associated with civil or criminal fines and penalties.
Compliance
with applicable environmental laws and regulations may be expensive, and current or future environmental laws and regulations may impair
our product development and research efforts. In addition, we cannot entirely eliminate the risk of accidental injury or contamination
from these materials or wastes. Although we maintain workers’ compensation insurance to cover us for costs and expenses we may
incur due to injuries to our employees resulting from the use of hazardous materials, this insurance may not provide adequate coverage
against potential liabilities. We do not carry specific biological or hazardous waste insurance coverage, and our property, casualty
and general liability insurance policies specifically exclude coverage for damages and fines arising from biological or hazardous waste
exposure or contamination. Accordingly, in the event of contamination or injury, we could be held liable for damages or be penalized
with fines in an amount exceeding our resources, and our clinical trials or regulatory approvals could be suspended, which could have
a material adverse effect on our business, financial condition, results of operations and prospects.
In
addition, we may incur substantial costs in order to comply with current or future environmental, health and safety laws, regulations
and permitting requirements. For example, our products are considered to contain genetically modified organisms or cells, which are regulated
in different ways depending upon the country in which preclinical research or clinical trials are conducted. These current or future
laws, regulations and permitting requirements may impair our research, development or production efforts. Failure to comply with these
laws, regulations and permitting requirements also may result in substantial fines, penalties or other sanctions or business disruption,
which could have a material adverse effect on our business, financial condition, results of operations and prospects.
Any
third-party contract research organizations, contract manufacturers and suppliers we engage will also be subject to these and other environmental,
health and safety laws and regulations. Liabilities they incur pursuant to these laws and regulations could result in significant costs
or an interruption in operations, which could have a material adverse effect on our business, financial condition, results of operations
and prospects.
Risks
Related to Regulatory Review
If
clinical trials of our product candidates fail to demonstrate safety and efficacy to the satisfaction of regulatory authorities or do
not otherwise produce positive results, we may incur additional costs or experience delays in completing, or ultimately be unable to
complete, the development and commercialization of such product candidates.
Before
obtaining marketing approval from regulatory authorities for the sale of JSP191 and any other product candidates we identify and develop,
we must complete preclinical development and then conduct extensive clinical trials to demonstrate the safety and efficacy of such product
candidates in humans. Clinical testing is expensive, difficult to design and implement, can take many years to complete and is uncertain
as to outcome. A failure of one or more clinical trials can occur at any stage of testing. The outcome of preclinical testing and early
clinical trials may not be predictive of the success of later clinical trials, and interim results of a clinical trial do not necessarily
predict final results. Moreover, preclinical and clinical data are often susceptible to varying interpretations and analyses. Many companies
that have believed their product candidates performed satisfactorily in preclinical studies and clinical trials have nonetheless failed
to obtain marketing approval of their product candidates.
We
and our collaborators, if any, may experience numerous unforeseen events during, or as a result of, clinical trials that could delay
or prevent our ability to receive marketing approval or commercialize any product candidates, including:
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● |
delays in reaching a consensus
with regulators on trial design; |
|
● |
regulators, IRBs, independent
ethics committees or scientific review boards may not authorize us or our investigators to commence a clinical trial or conduct a
clinical trial at a prospective trial site; |
|
● |
delays in reaching or failing
to reach agreement on acceptable clinical trial contracts or clinical trial protocols with prospective CROs and clinical trial sites; |
|
● |
clinical trials of product
candidates may produce negative or inconclusive results, and we may decide, or regulators may require us, to conduct additional clinical
trials or abandon product development or research programs; |
|
● |
difficulty in designing well-controlled
clinical trials due to ethical considerations that may render it inappropriate to conduct a trial with a control arm that can be
effectively compared to a treatment arm; |
|
● |
difficulty in designing clinical
trials and selecting endpoints for diseases that have not been well-studied and for which the natural history and course of the disease
is poorly understood; |
|
● |
the number of patients required
for clinical trials of JSP191 and any other product candidates we may develop may be larger than we anticipate; enrollment of suitable
participants in these clinical trials, which may be particularly challenging for some of the rare genetically defined diseases we
are targeting in our most advanced programs, may be delayed or slower than we anticipate; or patients may drop out of these clinical
trials at a higher rate than we anticipate; |
|
● |
our third-party contractors
may fail to comply with regulatory requirements or meet their contractual obligations to us in a timely manner, or at all; |
|
● |
regulators, IRBs or independent
ethics committees may require that we or our investigators suspend or terminate clinical research or clinical trials for various
reasons, including noncompliance with regulatory requirements, a finding of undesirable side effects or other unexpected characteristics,
or that the participants are being exposed to unacceptable health risks or after an inspection of our clinical trial operations or
trial sites; |
|
● |
the cost of clinical trials
may be greater than we anticipate; |
|
● |
the supply or quality of product
candidates or other materials necessary to conduct clinical trials may be insufficient or inadequate, including as a result of delays
in the testing, validation, manufacturing and delivery of product candidates to the clinical sites by us or by third parties with
whom we have contracted to perform certain of those functions; |
|
● |
delays in having patients complete
participation in a trial or return for post-treatment follow-up; |
|
● |
clinical trial sites dropping
out of a trial; |
|
● |
selection of clinical endpoints
that require prolonged periods of clinical observation or analysis of the resulting data; |
|
● |
occurrence of serious adverse
events associated with product candidates that are viewed to outweigh their potential benefits; |
|
● |
occurrence of serious adverse
events in trials of the same class of agents conducted by other sponsors; and |
|
● |
changes in regulatory requirements
and guidance that require amending or submitting new clinical protocols. |
If
we or our collaborators, if any, are required to conduct additional clinical trials or other testing of product candidates beyond those
that we currently contemplate, if we or our collaborators are unable to successfully complete clinical trials or other testing of product
candidates, or if the results of these trials or tests are not positive or are only modestly positive or if there are safety concerns,
we or our collaborators may:
|
● |
be delayed in obtaining marketing
approval for any such product candidates or not obtain marketing approval at all; |
|
● |
obtain approval for indications
or patient populations that are not as broad as intended or desired; |
|
● |
obtain approval with labeling
that includes significant use or distribution restrictions or safety warnings, including boxed warnings; |
|
● |
be subject to changes in the
way the product is administered; |
|
● |
be required to perform additional
clinical trials to support approval or be subject to additional post-marketing testing requirements; |
|
● |
have regulatory authorities
withdraw or suspend their approval of the product or impose restrictions on its distribution in the form of a Risk Evaluation and
Mitigation Strategy (“REMS”) or through modification to an existing REMS; |
|
● |
experience damage to our reputation. |
Product
development costs will also increase if we or our collaborators experience delays in clinical trials or other testing or in obtaining
marketing approvals. We do not know whether any clinical trials will begin as planned, will need to be restructured or will be completed
on schedule, or at all. Significant clinical trial delays also could shorten any periods during which we may have the exclusive right
to commercialize product candidates, could allow our competitors to bring products to market before we do and could impair our ability
to successfully commercialize product candidates, any of which may harm our business, financial condition, results of operations and
prospects.
Further,
disruptions at the FDA and other agencies may prolong the time necessary for new drugs to be reviewed and/or approved by necessary government
agencies, which would adversely affect our business. For example, over the last several years, the U.S. government has shut
down several times and certain regulatory agencies, including the FDA, have furloughed critical employees and stopped critical activities.
If a prolonged government shutdown occurs, it could significantly impact the ability of the FDA to timely review and process our regulatory
submissions, which could have a material adverse effect on our business. The Trump Administration also took several executive actions
that could impose significant burdens on, or otherwise materially delay, the FDA’s ability to engage in routine regulatory and
oversight activities. Certain of these orders were revoked by President Trump on January 20, 2021, and it remains to be seen how
the current administration will address regulatory reform.
Stem
cell transplant is a high-risk procedure with curative potential that may result in complications or adverse events for patients in our
clinical trials or for patients that use any of our product candidates, if approved.
Stem
cell transplant has the potential to cure patients across multiple diseases, but its use carries with it risks of toxicity, serious adverse
events and death. Because many of our therapies are used to prepare or treat patients undergoing stem cell transplant, patients in our
clinical trials or patients that use any of our product candidates may be subject to many of the risks that are currently inherent to
this procedure. In particular, stem cell transplant involves certain known potential post-procedure complications that may manifest several weeks
or months after a transplant and that may be more common in certain patient populations. For example, up to 20% of patients
with inherited metabolic disorders treated with a transplant experience primary engraftment failure, resulting in severe complications,
including death. Another example is autoimmune cytopenia, a known and severe frequent complication of the transplant procedure in patients
with non-malignant diseases, such as inherited metabolic diseases, that can result in death. There is also a risk of graft-versus-host
disease, a potentially serious complication in which the grafted cells attack and damage the patient’s healthy cells, which can
be severe and sometimes life-threatening. If these or other serious adverse events, undesirable side effects, or unexpected characteristics
are identified during the development of any of our product candidates, we may need to limit, delay or abandon our further clinical development
of those product candidates, even if such events, effects or characteristics were the result of stem cell transplant or related procedures
generally, and not directly or specifically caused or exacerbated by our product candidates. All serious adverse events or unexpected
side effects are continually monitored per the clinical trial’s approved protocol. If serious adverse events are determined to
be directly or specifically caused or exacerbated by our product candidates, we would follow the trial protocol’s requirements,
which call for our data safety monitoring committee to review all available clinical data in making a recommendation regarding the trial’s
continuation.
Failure
to obtain marketing approval in foreign jurisdictions would prevent any product candidates we develop from being marketed in such jurisdictions,
which, in turn, would materially impair our ability to generate revenue.
In
order to market and sell any product candidates we develop in the European Union and many other foreign jurisdictions, we or our collaborators
must obtain separate marketing approvals and comply with numerous and varying regulatory requirements. The approval procedure varies
among countries and can involve additional testing. The time required to obtain approval may differ substantially from that required
to obtain FDA approval. The regulatory approval process outside the United States generally includes all of the risks associated
with obtaining FDA approval. In addition, in many countries outside the United States, it is required that the product be approved
for reimbursement before the product can be approved for sale in that country. We or our collaborators may not obtain approvals from
regulatory authorities outside the United States on a timely basis, if at all. Approval by the FDA does not ensure approval by regulatory
authorities in other countries or jurisdictions, and approval by one regulatory authority outside the United States does not ensure
approval by regulatory authorities in other countries or jurisdictions or by the FDA. We may not be able to file for marketing approvals
and may not receive necessary approvals to commercialize our product candidates in any jurisdiction, which would materially impair our
ability to generate revenue.
Additionally,
we could face heightened risks with respect to seeking marketing approval in the United Kingdom as a result of the recent withdrawal
of the United Kingdom from the European Union on December 31, 2020, commonly referred to as Brexit. Pursuant to the formal withdrawal
arrangements agreed between the United Kingdom and the European Union, the United Kingdom withdrew from the European Union, effective
December 31, 2020. On December 24, 2020, the United Kingdom and European Union entered into a Trade and Cooperation Agreement.
The agreement sets out certain procedures for approval and recognition of medical products in each jurisdiction.
Since
the regulatory framework for pharmaceutical products in the United Kingdom covering the quality, safety, and efficacy of pharmaceutical
products, clinical trials, marketing authorization, commercial sales, and distribution of pharmaceutical products is derived from European
Union directives and regulations, Brexit could materially impact the future regulatory regime that applies to products and the approval
of product candidates in the United Kingdom. Any delay in obtaining, or an inability to obtain, any marketing approvals, as a result
of Brexit or otherwise, would prevent us from commercializing any product candidates in the United Kingdom and/or the European Union
and restrict our ability to generate revenue and achieve and sustain profitability. If any of these outcomes occur, we may be forced
to restrict or delay efforts to seek regulatory approval in the United Kingdom and/or the European Union for any product candidates,
which could significantly and materially harm our business.
Even
if we complete the necessary clinical trials, we cannot predict when, or if, we will obtain regulatory approval to commercialize our
product candidates in the United States or any other jurisdiction, and any such approval may be for a more narrow indication than
we seek.
We
cannot commercialize a product candidate until the appropriate regulatory authorities have reviewed and approved the product candidate.
Even if our product candidates meet their safety and efficacy endpoints in clinical trials, the regulatory authorities may not complete
their review processes in a timely manner, or we may not be able to obtain regulatory approval. Additional delays may result if an FDA
Advisory Committee or other regulatory authority recommends non-approval or restrictions on approval. In addition, we may experience
delays or rejections based upon additional government regulation from future legislation or administrative action, or changes in regulatory
authority policy during the period of product development, clinical trials and the review process.
Regulatory
authorities also may approve a product candidate for more limited indications than requested or they may impose significant limitations
in the form of narrow indications, warnings or a REMS. These regulatory authorities may require labeling that includes precautions
or contra-indications with respect to conditions of use, or they may grant approval subject to the performance of costly post-marketing
clinical trials. In addition, regulatory authorities may not approve the labeling claims that are necessary or desirable for the successful
commercialization of our product candidates. Any of the foregoing scenarios could materially harm the commercial prospects for our product
candidates and materially adversely affect our business, financial condition, results of operations and prospects.
Marketing
approval by the FDA in the United States, if obtained, does not ensure approval by regulatory authorities in other countries or
jurisdictions. In addition, clinical trials conducted in one country may not be accepted by regulatory authorities in other countries,
and regulatory approval in one country does not guarantee regulatory approval in any other country. Approval processes vary among countries
and can involve additional product candidate testing and validation and additional administrative review periods. Seeking foreign regulatory
approval could result in difficulties and costs for us and require additional preclinical studies or clinical trials, which could be
costly and time-consuming. Regulatory requirements can vary widely from country to country and could delay or prevent the introduction
of our product candidates we may develop in those countries. The foreign regulatory approval process involves all of the risks associated
with FDA approval. We do not have any product candidates approved for sale in any jurisdiction, including international markets, and
we do not have experience in obtaining regulatory approval in international markets. If we fail to comply with regulatory requirements
in international markets or to obtain and maintain required approvals, or if regulatory approvals in international markets are delayed,
our target market will be reduced and our ability to realize the full market potential of our product candidates will be unrealized.
Even
if we obtain regulatory approval of any of our product candidates, the approved products may be subject to post-approval studies and
will remain subject to ongoing regulatory requirements. If we fail to comply, or if concerns are identified in subsequent studies, our
approval could be withdrawn, and our product sales could be suspended.
If
we are successful at obtaining regulatory approval for JSP191 or any of our other product candidates, regulatory agencies in the U.S. and
other countries where a product will be sold may require extensive additional clinical trials or post-approval clinical trials that are
expensive and time-consuming to conduct. These studies may be expensive and time-consuming to conduct and may reveal side effects or
other harmful effects in patients that use our therapeutic products after they are on the market, which may result in the limitation
or withdrawal of our drugs from the market. Alternatively, we may not be able to conduct such additional trials, which might force us
to abandon our efforts to develop or commercialize certain product candidates. Even if post-approval studies are not requested or required,
after our products are approved and are on the market, there might be safety issues that emerge over time that require a change in product
labeling, additional post-market studies or clinical trials, imposition of distribution and use restrictions under a REMS or withdrawal
of the product from the market, which would cause our revenue to decline.
Additionally,
any products that we may successfully develop will be subject to ongoing regulatory requirements after they are approved. These requirements
will govern the manufacturing, packaging, marketing, distribution, and use of our products. If we fail to comply with such regulatory
requirements, approval for our products may be withdrawn, and product sales may be suspended. We may not be able to regain compliance,
or we may only be able to regain compliance after a lengthy delay, significant expense, lost revenues and/or damage to our reputation.
The
regulatory landscape that will govern our product candidates is uncertain; regulations relating to more established cellular therapy
products are still developing, and changes in regulatory requirements could result in delays or discontinuation of development of our
product candidates or unexpected costs in obtaining regulatory approval. The FDA and other governing bodies may disagree with our regulatory
plan, and we may fail to obtain regulatory approval of our product candidates.
Because
our product candidates and technology platform involve genetic and cellular engineering, we are subject to many of the challenges and
risks that other genetically engineered biologics and cellular therapies face, including:
|
● |
regulatory requirements or
guidance regarding the requirements governing genetic and cellular engineering products have changed and may continue to change in
the future; |
|
● |
to date, only a limited number
of products that involve genetic or cellular engineering have been approved globally; |
|
● |
improper modulation of a gene
sequence, including unintended alterations or insertion of a sequence into certain locations in a patient’s chromosomes, could
lead to cancer, other aberrantly functioning cells or other diseases, as well as death; |
|
● |
corrective expression of a
missing protein, or deletion of an existing protein, in patients’ cells could result in the protein or cell being recognized
as foreign, and lead to a sustained immunological reaction against the expressed protein or expressing cells, which could be severe
or life-threatening; |
|
● |
regulatory agencies may require
extended follow-up observation periods of patients who receive treatment using genetic or cellular engineering products including,
for example, the FDA’s recommended 15-year follow-up observation period for these patients, and we will need to adopt
such observation periods for our product candidates if required by the relevant regulatory agency, which could vary by country or
region; and |
|
● |
the fields of genetic and cellular
engineering are subject to a number of intellectual property disputes. |
The
regulatory requirements that will govern any eHSCs or other novel genetically engineered product candidates we develop may change. Within
the broader genetic medicine field, we are aware of a limited number of gene therapy products that have received marketing authorization
from the FDA and the EMA. Even with respect to more established products that fit into the categories of gene therapies or cell
therapies, the regulatory landscape is still developing. Regulatory requirements governing gene therapy products and cell therapy products
have changed frequently and will likely continue to change in the future. Moreover, there is substantial, and sometimes uncoordinated,
overlap in those responsible for regulation of existing gene therapy products and cell therapy products. For example, in the United States,
the FDA has established the Office of Tissues and Advanced Therapies (“OTAT”) within its Center for Biologics Evaluation
and Research (“CBER”) to consolidate the review of gene therapy and related products, and the Cellular, Tissue and Gene Therapies
Advisory Committee to advise CBER on its review. In addition to FDA oversight and oversight by IRBs under guidelines promulgated by the
National Institutes of Health (“NIH”), gene therapy clinical trials are also subject to review and oversight by an institutional
biosafety committee (“IBC”), a local institutional committee that reviews and oversees research utilizing recombinant or
synthetic nucleic acid molecules at that institution. Before a clinical study can begin at any institution, that institution’s
IRB and its IBC assess the safety of the research and identify any potential risk to public health or the environment. While
the NIH guidelines are not mandatory unless the research in question is being conducted at or sponsored by institutions receiving NIH
funding of recombinant or synthetic nucleic acid molecule research, many companies and other institutions not otherwise subject to the
NIH guidelines voluntarily follow them. Moreover, serious adverse events or developments in clinical trials of gene or cellular therapy
product candidates conducted by others may cause the FDA or other regulatory bodies to initiate a clinical hold on our clinical trials
or otherwise change the requirements for approval of any of our product candidates. Although the FDA decides whether individual gene
or cellular therapy protocols may proceed, the review process and determinations of other reviewing bodies can impede or delay the initiation
of a clinical trial even if the FDA has reviewed the trial and approved its initiation.
The
same applies in the European Union. The EMA’s Committee for Advanced Therapies (“CAT”) is responsible for assessing
the quality, safety and efficacy of advanced-therapy medicinal products. The role of the CAT is to prepare a draft opinion on an application
for marketing authorization for a cell or gene therapy or other novel therapeutic medicinal candidate that is submitted to the Committee
for Medicinal Products for Human Use (“CHMP”) before CHMP adopts its final opinion. In the European Union, the development
and evaluation of an advanced therapeutic medicinal product must be considered in the context of the relevant European Union guidelines.
The EMA may issue new guidelines concerning the development and marketing authorization for these medicinal products and require that
we comply with these new guidelines. As a result, the procedures and standards applied to gene and cell therapy products may be applied
to our eHSCs, but that remains uncertain at this point.
Adverse
developments in post-marketing experience or in clinical trials conducted by others of gene therapy products, cell therapy products or
products developed through the application of a genome engineering technology may cause the FDA, the EMA and other regulatory bodies
to revise the requirements for development or approval of our eHSCs may develop or limit the use of products utilizing genome engineering
technologies, either of which could materially harm our business. In addition, the clinical trial requirements of the FDA, the EMA and
other regulatory authorities and the criteria these regulators use to determine the safety and efficacy of a product candidate vary substantially
according to the type, complexity, novelty and intended use and market of the potential products. The regulatory approval process for
novel product candidates, such as our eHSCs, can be more expensive and take longer than for other, better known or more extensively studied
pharmaceutical or other product candidates. Regulatory agencies administering existing or future regulations or legislation may not allow
production and marketing of products utilizing genome engineering technology in a timely manner or under technically or commercially
feasible conditions. In addition, regulatory action or private litigation could result in expenses, delays or other impediments to our
product candidate development, research programs or the commercialization of resulting products.
The
regulatory review committees and advisory groups described above and the new guidelines they promulgate may lengthen the regulatory review
process, require us to perform additional studies or trials, increase our development costs, lead to changes in regulatory positions
and interpretations, delay or prevent approval and commercialization of these treatment candidates, or lead to significant post-approval
limitations or restrictions. Currently, OTAT requires a 15-year follow-up for each patient who receives a genetically engineered
cell or gene therapy. This requirement applies to all patients treated in trials during clinical development prior to approval. Following
approval, such prolonged follow-up could continue to be required. As we advance our product candidates and research programs, we will
be required to consult with these regulatory and advisory groups and to comply with applicable guidelines. If we fail to do so, we may
be required to delay or discontinue development of our eHSCs and any other product candidates we identify and develop.
Interim
“top-line” and preliminary results from our clinical trials that we may announce or publish from time to time may change
as more patient data become available and are subject to audit and verification procedures that could result in material changes in the
final data.
From
time to time, we may publish interim top-line or preliminary results from our preclinical studies and clinical trials, which are based
on a preliminary analysis of then-available data, and the results and related findings and conclusions are subject to change following
a more comprehensive review of the data related to the particular study or trial. In particular, we have announced, and may in the future
announce, interim results from our ongoing, open label Phase 1/2 and Phase 1 clinical trials of JSP191. Interim results from
clinical trials that we may complete are subject to the risk that one or more of the clinical outcomes may materially change as patient
enrollment continues and more patient data become available. Preliminary or top-line results also remain subject to audit and verification
procedures that may result in the final data being materially different from the preliminary data we previously published. As a result,
interim and preliminary data should be viewed with caution until the final data are available. Differences between preliminary or interim
data and final data could significantly harm our business prospects and may cause the trading price of our common stock to fluctuate
significantly.
Further,
others, including regulatory agencies, may not accept or agree with our assumptions, estimates, calculations, conclusions or analyses
or may interpret or weigh the importance of data differently, which could impact the value of the particular program, the approvability
or commercialization of the particular product candidate or product and us in general. In addition, the information we choose to publicly
disclose regarding a particular study or clinical trial is based on what is typically extensive information, investors or others may
not agree with what we determine is material or otherwise appropriate information to include in our disclosure, and any information we
determine not to disclose may ultimately be deemed significant with respect to future decisions, conclusions, views, activities or otherwise
regarding a particular product, product candidate or our business. If the interim, topline or preliminary data that we report differ
from actual results, or if others, including regulatory authorities, disagree with the conclusions reached, our ability to obtain approval
for, and commercialize, our product candidates may be harmed, which could harm our business, operating results, prospects or financial
condition.
Negative
public opinion of gene therapy and increased regulatory scrutiny of gene therapy and genetic research may adversely impact public perception
of our future product candidates.
Our
potential therapeutic products involve introducing genetic material into patients’ cells. The clinical and commercial success of
our potential products will depend in part on public acceptance of the use of gene therapy and gene regulation for the prevention or
treatment of human diseases. Public attitudes may be influenced by claims that gene therapy and gene regulation are unsafe, unethical
or immoral, and, consequently, our products may not gain the acceptance of the public or the medical community. Adverse public attitudes
may adversely impact our ability to enroll clinical trials. Moreover, our success will depend upon physicians prescribing, and their
patients being willing to receive, treatments that involve the use of product candidates we may develop in lieu of, or in addition to,
existing treatments with which they are already familiar and for which greater clinical data may be available.
More
restrictive government regulations or negative public opinion would have a negative effect on our business or financial condition and
may delay or impair the development and commercialization of our product candidates or demand for any products once approved. For example,
in 2003, trials using early versions of murine gamma-retroviral vectors, which integrate with, and thereby alter, the host cell’s
DNA, have led to several well-publicized adverse events, including reported cases of leukemia. Adverse events in our clinical trials,
even if not ultimately attributable to our product candidates, and the resulting publicity could result in increased governmental regulation,
unfavorable public perception, potential regulatory delays in the testing or approval of our product candidates, stricter labeling requirements
for those product candidates that are approved, and a decrease in demand for any such product candidates. The risk of cancer remains
a concern for gene therapy, and we cannot assure that it will not occur in any of our planned or future clinical trials. In addition,
there is the potential risk of delayed adverse events following exposure to gene therapy products due to persistent biological activity
of the genetic material or other components of products used to carry the genetic material. If any such adverse events occur, commercialization
of our product candidates or further advancement of our clinical trials could be halted or delayed, which would have a negative impact
on our business and operations.
We
may seek Fast Track or other accelerated review designations for some or all of our product candidates. We may not receive such designation,
and even for those product candidates for which we do, it may not lead to a faster development or regulatory review or approval process,
and will not increase the likelihood that product candidates will receive marketing approval.
We
may seek Fast Track or other accelerated review designations for some or all of our other product candidates. If a drug or biologic is
intended for the treatment of a serious or life-threatening condition or disease, and nonclinical or clinical data demonstrate the potential
to address an unmet medical need, the product may qualify for FDA Fast Track designation, for which sponsors must apply. If granted,
a Fast Track or other accelerated review designation makes a product candidate eligible for more frequent interactions with the FDA to
discuss the development plan and clinical trial design, as well as rolling review of the application, which means that we can submit
completed sections of our marketing application for review prior to completion of the entire submission. Marketing applications of product
candidates with a Fast Track or other accelerated review designation may qualify for priority review under the policies and procedures
offered by the FDA, but a Fast Track or other accelerated review designation does not assure any such qualification or ultimate marketing
approval by the FDA. The FDA has broad discretion with respect to whether or not to grant this designation. Thus, even if we believe
a particular product candidate is eligible for this designation, the FDA may decide not to grant it. Moreover, even if we do receive
a Fast Track or another accelerated review designation, we or our collaborators may not experience a faster development process, review
or approval compared to conventional FDA procedures. In addition, the FDA may withdraw a Fast Track or other accelerated review designation
if it believes that the designation is no longer supported by data from our clinical development program.
We
may seek priority review designation for our product candidates, but we might not receive such designation, and even if we do, such designation
may not lead to a faster development or regulatory review or approval process.
If
the FDA determines that a product candidate offers a treatment for a serious condition and, if approved, the product would provide a
significant improvement in safety or effectiveness, the FDA may designate the product candidate for priority review. A priority review
designation means that the goal for the FDA to review an application is six months, rather than the standard review period of ten months.
The FDA has broad discretion with respect to whether or not to grant priority review status to a product candidate, so even if we believe
a particular product candidate is eligible for such designation or status, the FDA may decide not to grant it. Moreover, a priority review
designation does not necessarily mean a faster development or regulatory review or approval process or necessarily confer any advantage
with respect to approval compared to conventional FDA procedures. Receiving priority review from the FDA does not guarantee approval
within the six-month review cycle or at all.
A Breakthrough
Therapy Designation by the FDA, even if granted for any of our product candidates, may not lead to a faster development or regulatory
review or approval process, and it does not increase the likelihood that our product candidates will receive marketing approval.
We
may seek a Breakthrough Therapy Designation for our product candidates if the clinical data support such a designation for one or more
product candidates. A breakthrough therapy is defined as a drug or biologic that is intended, alone or in combination with one or more
other drugs or biologics, to treat a serious or life-threatening disease or condition and preliminary clinical evidence indicates that
the drug, or biologic, may demonstrate substantial improvement over existing therapies on one or more clinically significant endpoints,
such as substantial treatment effects observed early in clinical development. For product candidates that have been designated as breakthrough
therapies, interaction and communication between the FDA and the sponsor of the trial can help to identify the most efficient path for
clinical development while minimizing the number of patients placed in ineffective control regimens. Drugs and biologics designated as
breakthrough therapies by the FDA may also be eligible for accelerated approval.
Designation
as a breakthrough therapy is within the discretion of the FDA. Accordingly, even if we believe one of our product candidates meets
the criteria for designation as a breakthrough therapy, the FDA may disagree and determine not to make such designation. In any event,
the receipt of a Breakthrough Therapy Designation for a product candidate may not result in a faster development process, review or approval
compared to drugs considered for approval under non-expedited FDA review procedures and does not assure ultimate approval by the FDA. In
addition, even if one or more of our product candidates qualify as breakthrough therapies, the FDA may later decide that the product
no longer meets the conditions for such qualification.
The
regenerative medicine advanced therapy (“RMAT”) designation by the FDA for any of our product candidates may not lead to
a faster development or regulatory review or approval process, and it does not increase the likelihood that our product candidates will
receive marketing approval.
We
may seek an RMAT designation for our product candidates if the clinical data support such a designation for one or more product candidates.
An RMAT is defined as cell and gene therapies, therapeutic tissue engineering products, human cell and tissue products, and combination
products using any such therapies or products. Gene therapies, including genetically modified cells that lead to a durable modification
of cells or tissues may meet the definition of a regenerative medicine therapy. The RMAT program is intended to facilitate efficient
development and expedite review of RMATs, which are intended to treat, modify, reverse, or cure a serious or life-threatening disease
or condition and for which preliminary clinical evidence indicates that the drug has the potential to address unmet medical needs for
such disease or condition. A biologics license application for a regenerative medicine therapy that has received RMAT designation may
be eligible for priority review or accelerated approval. An RMAT may be eligible for priority review if it treats a serious condition
and, if approved, would provide a significant improvement in the safety or effectiveness of the treatment of the condition. An RMAT may
be eligible for accelerated approval through surrogate or intermediate endpoints reasonably likely to predict long-term clinical benefit
or reliance upon data obtained from a meaningful number of sites. Benefits of such designation also include early interactions with the
FDA to discuss any potential surrogate or intermediate endpoint to be used to support accelerated approval. A regenerative medicine therapy
with RMAT designation that is granted accelerated approval and is subject to post-approval requirements may fulfill such requirements
through the submission of clinical evidence from clinical trials, patient registries, or other sources of real world evidence, such as
electronic health records; the collection of larger confirmatory data sets; or post-approval monitoring of all patients treated with
such therapy prior to its approval.
Designation
as an RMAT is within the discretion of the FDA. Accordingly, even if we believe one of our product candidates meets the criteria
for designation as a RMAT, the FDA may disagree and instead determine not to make such designation. In any event, the receipt of RMAT
designation for our product candidates may not result in a faster development process, review or approval compared to drugs considered
for approval under conventional FDA procedures and does not assure ultimate approval by the FDA. In addition, even if one or more
of our product candidates qualify for RMAT designation, the FDA may later decide that the biological products no longer meet the conditions
for such qualification.
We
may not be able to obtain orphan drug exclusivity for one or more of our product candidates, and even if we do, that exclusivity may
not prevent the FDA or EMA from approving other competing products.
Under
the Orphan Drug Act of 1983, the FDA may designate a product as an orphan drug if it is a drug or biologic intended to treat
a rare disease or condition. A similar regulatory scheme governs approval of orphan products by the EMA in the European Union. Generally,
if a product candidate with an orphan drug designation subsequently receives the first marketing approval for the indication for which
it has such designation, the product is entitled to a period of marketing exclusivity, which precludes the FDA or EMA from approving
another marketing application for the same product for the same therapeutic indication for that time period. The applicable period is
seven years in the United States and ten years in the European Union. The exclusivity period in the European Union can
be reduced to six years if a product no longer meets the criteria for orphan drug designation, in particular if the product is sufficiently
profitable so that market exclusivity is no longer justified.
In
order for the FDA to grant orphan drug exclusivity to one of our products, the FDA must find that the product is indicated for the treatment
of a condition or disease with a patient population of fewer than 200,000 individuals annually in the United States. The FDA may
conclude that the condition or disease for which we may seek orphan drug exclusivity does not meet this standard. Even if we obtain orphan
drug exclusivity for a product, that exclusivity may not effectively protect the product from competition because different products
can be approved for the same condition. In particular, the concept of what constitutes the “same drug” for purposes of orphan
drug exclusivity remains in flux in the context of gene therapies, and the FDA issued recent draft guidance suggesting that it would
not consider two genetic medicine products to be different drugs solely based on minor differences in the transgenes or vectors within
a given vector class. In addition, even after an orphan drug is approved, the FDA can subsequently approve the same product for the same
condition if the FDA concludes that the later product is clinically superior in that it is shown to be safer, more effective or makes
a major contribution to patient care. Orphan drug exclusivity may also be lost if the FDA or EMA determines that the request for designation
was materially defective or if the manufacturer is unable to assure sufficient quantity of the product to meet the needs of the patients
with the rare disease or condition.
In
2017, Congress passed the FDA Reauthorization Act of 2017 (the “FDARA”). FDARA, among other things, codified the
FDA’s pre-existing regulatory interpretation to require that a drug sponsor demonstrate the clinical superiority of an orphan drug
that is otherwise the same as a previously approved drug for the same rare disease in order to receive orphan drug exclusivity. Under
omnibus legislation signed by President Trump on December 27, 2020, the requirement for a product to show clinical superiority applies
to any drug and biologic that received orphan drug designation before enactment of FDARA in 2017 but has not yet been approved or licensed
by the FDA. We do not know if, when, or how the FDA may change the orphan drug regulations and policies in the future, and it is
uncertain how any changes might affect our business. Depending on what changes the FDA may make to its orphan drug regulations and policies,
our business could be adversely impacted.
Disruptions
at the FDA and other government agencies caused by funding shortages or global health concerns could hinder their ability to hire, retain
or deploy key leadership and other personnel, or otherwise prevent new or modified products from being developed, approved or commercialized
in a timely manner or at all, which could negatively impact our business.
The
ability of the FDA to review and approve new products can be affected by a variety of factors, including government budget and funding
levels, statutory, regulatory, and policy changes, the FDA’s ability to hire and retain key personnel and accept the payment of
user fees, and other events that may otherwise affect the FDA’s ability to perform routine functions. Average review times at the
agency have fluctuated in recent years as a result. In addition, government funding of other government agencies that fund research
and development activities is subject to the political process, which is inherently fluid and unpredictable. Disruptions at the FDA and
other agencies may also slow the time necessary for new biologics or modifications to cleared or approved biologics to be reviewed and/or
approved by necessary government agencies, which would adversely affect our business. For example, over the last several years,
including for 35 days beginning on December 22, 2018, the U.S. government has shut down several times and certain
regulatory agencies, such as the FDA, have furloughed critical FDA employees and stopped critical activities. If a prolonged government
shutdown occurs, it could significantly impact the ability of the FDA to timely review and process our regulatory submissions, which
could have a material adverse effect on our business.
Separately,
in response to the COVID-19 pandemic, on March 10, 2020, the FDA announced its intention to postpone most inspections of foreign
manufacturing facilities, and on March 18, 2020, the FDA temporarily postponed routine surveillance inspections of domestic manufacturing
facilities. Subsequently, on July 10, 2020, the FDA announced its intention to resume certain on-site inspections of domestic manufacturing
facilities subject to a risk-based prioritization system. Regulatory authorities outside the United States may adopt similar restrictions
or other policy measures in response to the COVID-19 pandemic. If a prolonged government shutdown occurs, or if global health concerns
continue to prevent the FDA or other regulatory authorities from conducting their regular inspections, reviews, or other regulatory activities,
it could significantly impact the ability of the FDA or other regulatory authorities to timely review and process our regulatory submissions,
which could have a material adverse effect on our business.
Risks
Related to Our Relationships with Third Parties
We
rely on third parties to conduct our preclinical and clinical trials and will rely on them to perform other tasks for us. If these third
parties do not successfully carry out their contractual duties, meet expected deadlines or comply with regulatory requirements, we may
not be able to obtain regulatory approval for or commercialize our product candidates and our business could be substantially harmed.
Although
we have recruited a team that has experience with clinical trials, as a company, we have limited experience in conducting clinical trials.
Moreover, we do not have the ability to independently conduct preclinical studies and clinical trials, and we have relied upon, and plan
to continue to rely upon, medical institutions, clinical investigators, contract laboratories and other third parties, or our CROs, to
conduct preclinical studies and future clinical trials for our product candidates. We expect to rely heavily on these parties for execution
of preclinical and future clinical trials for our product candidates and control only certain aspects of their activities. Nevertheless,
we will be responsible for ensuring that each of our preclinical and clinical trials is conducted in accordance with the applicable protocol,
legal and regulatory requirements and scientific standards and our reliance on CROs will not relieve us of our regulatory responsibilities.
For any violations of laws and regulations during the conduct of our preclinical studies and clinical trials, we could be subject to
warning letters or enforcement action that may include civil penalties up to and including criminal prosecution.
We
and our CROs will be required to comply with regulations, including cGCPs for conducting, monitoring, recording and reporting the results
of preclinical and clinical trials to ensure that the data and results are scientifically credible and accurate and that the trial patients
are adequately informed of the potential risks of participating in clinical trials and their rights are protected. These regulations
are enforced by the FDA, the Competent Authorities of the Member States of the European Economic Area and comparable foreign regulatory
authorities for any drugs in clinical development. The FDA enforces cGCP regulations through periodic inspections of clinical trial sponsors,
principal investigators and trial sites. If we or our CROs fail to comply with applicable cGCPs, the clinical data generated in our clinical
trials may be deemed unreliable and the FDA or comparable foreign regulatory authorities may require us to perform additional clinical
trials before approving our marketing applications. We cannot assure you that, upon inspection, the FDA will determine that any of our
future clinical trials will comply with cGCPs. In addition, our clinical trials must be conducted with product candidates produced in
accordance with the requirements in the FDA’s current cGMPs requirements. Our failure or the failure of our CROs to comply with
these regulations may require us to repeat clinical trials, which would delay the regulatory approval process and could also subject
us to enforcement action.
Although
we intend to design our planned clinical trials for our product candidates, for the foreseeable future CROs will conduct all of our planned
clinical trials. As a result, many important aspects of our development programs, including their conduct and timing, will be outside
of our direct control. Our reliance on third parties to conduct future preclinical studies and clinical trials will also result in less day-to-day
control over the management of data developed through preclinical studies and clinical trials than would be the case if we were relying
entirely upon our own staff.
If
any of our relationships with these third-party CROs terminate, we may not be able to enter into arrangements with alternative CROs.
If CROs do not successfully carry out their contractual duties or obligations or meet expected deadlines, if they need to be replaced
or if the quality or accuracy of the clinical data they obtain is compromised due to the failure to adhere to our clinical protocols,
regulatory requirements or for other reasons, any preclinical studies or clinical trials with which such CROs are associated with may
be extended, delayed or terminated. In such cases, we may not be able to obtain regulatory approval for or successfully commercialize
our product candidates. As a result, our financial results and the commercial prospects for our product candidates in the subject indication
could be harmed, our costs could increase and our ability to generate revenue could be delayed.
We
currently rely on a single manufacturer for our clinical supply of our product candidates. In the event of a loss of this manufacturer,
or a failure by such manufacturer to comply with FDA regulations, we may not be able to find an alternative source on commercially reasonable
terms, or at all. In addition, third-party manufacturers and any third-party collaborators may be unable to successfully scale-up manufacturing
of our current or future product candidates in sufficient quality and quantity, which would delay or prevent us from developing our product
candidates and commercializing approved products, if any.
We
do not have any manufacturing facilities at the present time. We currently rely on third-party manufacturers, including Lonza Sales AG
(“Lonza”) as a single source supplier, for the manufacture and supply of our materials for preclinical studies, and expect
to continue to do so for future clinical testing and for commercial supply of JSP191 and any other product candidates that we may develop
and for which we or our collaborators obtain marketing approval. Our agreement with Lonza includes certain limitations on our ability
to enter into supply arrangements with any other supplier without Lonza’s consent. In addition, Lonza has the right to increase
the prices it charges us for certain supplies depending on a number of factors, some of which are outside of our control. We may be unable
to maintain or establish any agreements with third-party manufacturers or suppliers or to do so on acceptable terms. Even if we are able
to establish agreements with third-party manufacturers or suppliers, reliance on third-party manufacturers entails additional risks,
including:
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the possible breach of the
manufacturing or supply agreement by the third party; |
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the possible termination or
nonrenewal of the agreement by the third party at a time that is costly or inconvenient for us; and |
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reliance on the third party
for regulatory compliance, quality assurance, safety and pharmacovigilance and related reporting. |
In
addition, pursuant to our Exclusive License Agreement with Amgen Inc., Lonza Biologics, Inc. has been engaged to manufacture JSP191 for
us. The agreement provides that in the event we wish to change the manufacturer of JSP191 to a different party, we must obtain Amgen
Inc.’s prior consent. As a result, our ability to obtain any alternative supplier of JSP191 may be further limited.
Third-party
manufacturers may not be able to comply with cGMP regulations or similar regulatory requirements outside the United States. Our
failure, or the failure of our third-party manufacturers or suppliers, to comply with applicable regulations could result in sanctions
being imposed on us, including fines, injunctions, civil penalties, delays, suspension or withdrawal of approvals, license revocations,
seizures or recalls of product candidates or products, operating restrictions and criminal prosecutions, any of which could significantly
and adversely affect supplies of our products and harm our business, financial condition, results of operations and prospects.
Our
product candidates may compete with other product candidates and products for access to manufacturing facilities and other supplies.
There are a limited number of manufacturers that operate under cGMP regulations and that might be capable of manufacturing for us. Also,
prior to the approval of our product candidates, we would need to identify a contract manufacturer that could produce our products at
a commercial scale and that could successfully complete FDA pre-approval inspection and inspections by other health authorities. Agreements
with such manufacturers or suppliers may not be available to us at the time we would need to have that capability and capacity.
Any
performance failure on the part of our existing or future manufacturers or suppliers, or any decision by a manufacturer or supplier to
remove our products from the market or restrict access to our products, could delay clinical development or marketing approval. We do
not currently have arrangements in place for redundant or guaranteed supply for many of the materials we currently use in our clinical
trials or preclinical studies, and we may have difficulty or be unable to establish alternative sources of these materials.
We
may enter into collaborations with third parties for the research, development and commercialization of certain product candidates we
may develop. If any such collaborations are not successful, we may not be able to capitalize on the market potential of those product
candidates.
We
may seek third-party collaborators for the research, development and commercialization of certain product candidates we may develop.
If we enter into any such arrangements with any third parties, we will likely have limited control over the amount and timing of resources
that our collaborators dedicate to the development or commercialization our product candidates. Our ability to generate revenues from
these arrangements will depend on our collaborators’ abilities to successfully perform the functions assigned to them in these
arrangements. We cannot predict the success of any collaboration that we enter into.
Collaborations
involving our current or future product candidates or research programs pose numerous risks to us, including the following:
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Collaborators may not pursue
development and commercialization of our product candidates or may elect not to continue or renew development or commercialization
programs based on clinical trial results, changes in the collaborator’s strategic focus or available funding or external factors
such as an acquisition that diverts resources or creates competing priorities. |
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Collaborators may delay clinical
trials, provide insufficient funding for a clinical trial program, stop a clinical trial or abandon a product candidate, repeat or
conduct new clinical trials or require a new formulation of a product candidate for clinical testing. |
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Collaborators could independently
develop, or develop with third parties, products that compete directly or indirectly with our product candidates if the collaborators
believe that competitive products are more likely to be successfully developed or can be commercialized under terms that are more
economically attractive than ours. |
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Collaborators with marketing
and distribution rights to one or more products may not commit sufficient resources to the marketing and distribution of such products. |
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Collaborators may not properly
obtain, maintain, enforce or defend our intellectual property or proprietary rights or may use our proprietary information in such
a way as to invite litigation that could jeopardize or invalidate our proprietary information or expose us to potential litigation. |
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Disputes may arise between
the collaborators and us that result in the delay or termination of the research, development or commercialization of our products
or product candidates or that result in costly litigation or arbitration that diverts management attention and resources. |
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We may lose certain valuable
rights under circumstances identified in our collaborations, including if we undergo a change of control. |
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Collaboration agreements may
not lead to development or commercialization of product candidates in the most efficient manner or at all. If a present or future
collaborator of ours were to be involved in a business combination, the continued pursuit and emphasis on our product development
or commercialization program under such collaboration could be delayed, diminished or terminated. |
If
our collaborations do not result in the successful development and commercialization of product candidates, or if one of our collaborators
terminates our agreement with us, we may not receive any future research funding or milestone or royalty payments under the collaboration.
If we do not receive the funding we expect under these agreements, our development of product candidates could be delayed, and we may
need additional resources to develop product candidates. In addition, if one of our collaborators terminates its agreement with us, we
may find it more difficult to find a suitable replacement collaborator or attract new collaborators, and our development programs may
be delayed or the perception of us in the business and financial communities could be adversely affected. All of the risks relating to
product development, regulatory approval and commercialization described in this Annual Report on Form 10-K apply to the activities of
our collaborators.
These
relationships, or those like them, may require us to incur non-recurring and other charges, increase our near- and long-term expenditures,
issue securities that dilute our existing stockholders, or disrupt our management and business.
If
we are not able to establish collaborations on commercially reasonable terms, we may have to alter our development and commercialization
plans.
Our
product development and research programs and the potential commercialization of JSP191 or any other product candidates we may develop
will require substantial additional cash to fund expenses. For some of the product candidates we may develop, we may decide to collaborate
with other pharmaceutical and biotechnology companies for the development and potential commercialization of those product candidates.
We
would face significant competition in seeking appropriate collaborators. Whether we reach a definitive agreement for a collaboration
will depend, among other things, upon our assessment of the collaborator’s resources and expertise, the terms and conditions of
the proposed collaboration, and the proposed collaborator’s evaluation of a number of factors. Those factors may include the design
or results of clinical trials, the likelihood of approval by the FDA, the EMA or similar regulatory authorities outside the United States,
the potential market for the subject product candidate, the costs and complexities of manufacturing and delivering such product candidate
to patients, the potential of competing products, the existence of uncertainty with respect to our ownership of technology, which can
exist if there is a challenge to such ownership without regard to the merits of the challenge, and industry and market conditions generally.
The collaborator may also consider alternative product candidates or technologies for similar indications that may be available to collaborate
on and whether such a collaboration could be more attractive than the one with us.
We
may also be restricted under existing collaboration agreements from entering into future agreements on certain terms with potential collaborators.
Collaborations are complex and time-consuming to negotiate and document. In addition, there have been a significant number of recent
business combinations among large pharmaceutical companies that have resulted in a reduced number of potential future collaborators.
We
may not be able to negotiate collaborations on a timely basis, on acceptable terms, or at all. If we are unable to do so, we may have
to curtail the development of the product candidate for which we are seeking to collaborate, reduce or delay our development program
or one or more of our other development programs, delay our potential commercialization or reduce the scope of any sales or marketing
activities, or increase our expenditures and undertake development or commercialization activities at our own expense. If we elect to
increase our expenditures to fund development or commercialization activities on our own, we may need to obtain additional capital, which
may not be available to us on acceptable terms or at all. If we do not have sufficient funds, we may not be able to develop product candidates
or bring them to market and generate product revenue.
Risks
Related to Our Intellectual Property
We
are highly dependent on intellectual property licensed from third parties, and termination of any of these licenses could result in the
loss of significant rights, which would harm our business.
We
are dependent on the patents, know-how and proprietary technology licensed from third parties for the development and, if approved, commercialization
of JSP191. Any termination of these licenses, or a finding that such intellectual property lacks legal effect, could result in the loss
of significant rights and could harm our ability to commercialize our current or future product candidates.
For
example, we rely on our worldwide exclusive license agreement with Amgen Inc., whereby we license a patent portfolio from Amgen Inc.
applicable to our targeted conditioning program that contains patent families directed to humanized C-kit antibody. We also rely on our
license agreement with Stanford, whereby we license a patent portfolio applicable to our targeted conditioning and stem cell graft programs
that contains patent families directed to immunodepletion of endogenous stem cell niche for engraftment.
Each
of our license agreements with third parties impose certain obligations on us, including obligations to use diligent efforts to meet
development thresholds and payment obligations. Non-compliance with such obligations may result in termination of the respective license
agreement or in legal and financial consequences. If any of our licensors terminates its respective license agreement, we may not be
able to develop or commercialize JSP191 or any other product candidates covered by these agreements. Termination of our license agreements
or reduction or elimination of our rights under them may result in us having to negotiate a new or reinstated agreement, which may not
be available to us on equally favorable terms, or at all, which may mean we are unable to develop, commercialize or sell the affected
product candidate or may cause us to lose our rights under the agreement.
In
addition, our licensors may make decisions in prosecuting, maintaining, enforcing and defending any licensed intellectual property rights
that may not be in our best interest. Moreover, if our licensors take any action with respect to any licensed intellectual property rights,
for example, any licensed patents or patent applications, that results in a successful challenge to the licensed intellectual property
by a third party, such patents may be invalidated or held to be unenforceable, and we may lose our rights under such patents, which could
materially harm our business.
Further,
the agreements under which we currently license intellectual property from third parties are complex, and certain provisions in such
agreements may be susceptible to multiple interpretations. Accordingly, disputes may arise between us and our licensors regarding intellectual
property subject to a license agreement. The resolution of any contract interpretation disagreement that may arise could narrow what
we believe to be the scope of our rights to the relevant intellectual property or technology, or increase what we believe to be our financial
or other obligations under the relevant agreement. If disputes over intellectual property that we have licensed prevent or impair our
ability to maintain our current licensing arrangements on acceptable terms, or are insufficient to provide us with the necessary rights
to use the intellectual property, we may be unable to successfully develop and commercialize the affected product candidates.
Our
commercial success depends on our ability to obtain, maintain and protect our intellectual property and proprietary technology.
Our
commercial success depends in large part on our ability to obtain, maintain and protect intellectual property rights through patents,
trademarks and trade secrets in the United States and other countries with respect to our proprietary product candidates. If we
do not adequately protect our intellectual property rights, competitors may be able to erode, negate or preempt any competitive advantage
we may have, which could harm our business and ability to achieve profitability.
To
protect our proprietary position, we own and have in-licensed certain intellectual property rights, including certain issued patents
and patent applications, and have filed and may file provisional and non-provisional patent applications in the United States or
abroad related to our product candidates that are important to our business. Provisional patent applications are not eligible to become
issued patents until, among other things, we file a non-provisional patent application within 12 months of the filing of one
or more of our related provisional patent applications. If we do not timely file non-provisional patent applications, we may lose our
priority date with respect to our provisional patent applications and any patent protection on the inventions disclosed in our provisional
patent applications. While we intend to timely file non-provisional patent applications relating to our provisional patent applications,
we cannot predict whether any such patent applications will result in the issuance of patents that provide us with any competitive advantage.
Moreover, the patent application and approval process is expensive and time-consuming. We may not be able to file and prosecute all necessary
or desirable patent applications at a reasonable cost or in a timely manner.
The
patent application, prosecution, and enforcement processes are subject to numerous risks and uncertainties, and there can be no assurance
that we, our licensors, or any of our future collaborators will be successful in protecting our product candidates by obtaining, defending,
and/or asserting patent rights. These risks and uncertainties include the following:
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the U.S. Patent and Trademark
Office (the “USPTO”) and various foreign governmental patent agencies require compliance with a number of procedural,
documentary, fee payment and other provisions during the patent process. There are situations in which noncompliance can result in
abandonment or lapse of a patent or patent application, resulting in partial or complete loss of patent rights in the relevant jurisdiction.
In such an event, competitors might be able to enter the market earlier than would otherwise have been the case; |
|
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patent applications may not
result in any patents being issued; |
|
● |
patents that may be issued
or in-licensed may be challenged, invalidated, modified, revoked, circumvented, found to be unenforceable or otherwise may not provide
any competitive advantage; |
|
● |
our competitors, many of whom
have substantially greater resources and many of whom have made significant investments in competing technologies, may seek or may
have already obtained patents that will limit, interfere with or eliminate our ability to make, use, and sell our potential product
candidates; |
|
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there may be significant pressure
on the U.S. government and international governmental bodies to limit the scope of patent protection both inside and outside
the United States for disease treatments that prove successful, as a matter of public policy regarding worldwide health concerns;
and |
|
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countries other than the United States
may have patent laws less favorable to patentees than those upheld by U.S. courts, allowing foreign competitors a better opportunity
to create, develop and market competing product candidates. |
In
some instances, agreements through which we license intellectual property rights may not give us control over patent prosecution or maintenance,
so that we may not be able to control which claims or arguments are presented, how claims are amended, and may not be able to secure,
maintain or successfully enforce necessary or desirable patent protection from those patent rights. We cannot be certain that patent
prosecution and maintenance activities by our licensors have been or will be conducted in compliance with applicable laws and regulations
or will result in valid and enforceable patents.
Moreover,
some of our in-licensed patents and patent applications may be, and some of our future owned and licensed patents may be, co-owned with
third parties. If we are unable to obtain an exclusive license to any such third-party co-owners’ interest in such patents or patent
applications, such co-owners may be able to license their rights to other third parties, including our competitors, and our competitors
could market competing products and technology. In addition, we may need the cooperation of any such co-owners of our patents in order
to enforce such patents against third parties, and such cooperation may not be provided to us.
The
patent protection we obtain for our product candidates may not be sufficient enough to provide us with any competitive advantage or our
patents may be challenged.
Our
owned and licensed patents and pending patent applications, if issued, may not provide us with any meaningful protection or may not prevent
competitors from designing around our patent claims to circumvent our patents by developing similar or alternative technologies or therapeutics
in a non-infringing manner. For example, a third party may develop a competitive product that provides benefits similar to one or more
of our product candidates but falls outside the scope of our patent protection or license rights. If the patent protection provided by
the patents and patent applications we hold or pursue with respect to our product candidates is not sufficiently broad to impede such
competition, our ability to successfully commercialize our product candidates could be negatively affected, which would harm our business.
Currently, a significant portion of our patents and patent applications are in-licensed, though similar risks would apply to any patents
or patent applications that we now own or may own or in-license in the future.
It
is possible that defects of form in the preparation or filing of our patents or patent applications may exist, or may arise in the future,
for example with respect to proper priority claims, inventorship, claim scope or requests for patent term adjustments. If we or our partners,
collaborators, licensees or licensors, whether current or future, fail to establish, maintain or protect such patents and other intellectual
property rights, such rights may be reduced or eliminated. If our partners, collaborators, licensees or licensors, are not fully cooperative
or disagree with us as to the prosecution, maintenance or enforcement of any patent rights, such patent rights could be compromised.
If there are material defects in the form, preparation, prosecution or enforcement of our patents or patent applications, such patents
may be invalid and/or unenforceable, and such applications may never result in valid, enforceable patents. Any of these outcomes could
impair our ability to prevent competition from third parties, which may have an adverse impact on our business.
In
addition, the determination of patent rights with respect to clinical compositions of matter and treatment methods commonly involves
complex legal and factual questions, which are dependent upon the current legal and intellectual property context, extant legal precedent
and interpretations of the law by individuals. As a result, the issuance, scope, validity, enforceability and commercial value of our
patent rights are characterized by uncertainty.
Changes
in either the patent laws or interpretation of the patent laws in the United States and other countries may diminish the value of
our patents or narrow the scope of our patent protection. In addition, the laws of foreign countries may not protect our rights to the
same extent or in the same manner as the laws of the United States. For example, patent laws in various jurisdictions, including
significant commercial markets such as Europe, restrict the patentability of methods of treatment of the human body more than U.S. law
does. If these changes were to occur, they could have a material adverse effect on our ability to generate revenue.
Pending
patent applications cannot be enforced against third parties practicing the technology claimed in such applications unless and until
a patent issues from such applications. Assuming the other requirements for patentability are met, currently, the first party to file
a patent application is generally entitled to the patent. However, prior to March 16, 2013, in the United States, the first
party to invent was entitled to the patent. Publications of discoveries in the scientific literature often lag behind the actual discoveries,
and patent applications in the United States and other jurisdictions are not published until 18 months after filing, or
in some cases not at all. Therefore, we cannot be certain that we were the first to make the inventions claimed in our patents or pending
patent applications, or that we were the first to file for patent protection of such inventions. Similarly, we cannot be certain that
parties from whom we do or may license or purchase patent rights were the first to make relevant claimed inventions, or were the first
to file for patent protection for them. If third parties have filed prior patent applications on inventions claimed in our patents or
applications that were filed on or before March 15, 2013, an interference proceeding in the United States can be initiated
by such third parties to determine who was the first to invent any of the subject matter covered by the patent claims of our applications.
If third parties have filed such prior applications after March 15, 2013, a derivation proceeding in the United States can
be initiated by such third parties to determine whether our invention was derived from theirs.
Moreover,
because the issuance of a patent is not conclusive as to its inventorship, scope, validity or enforceability, our owned and licensed
patents or pending patent applications may be challenged in the courts or patent offices in the United States and abroad. There
is no assurance that all of the potentially relevant prior art relating to our patents and patent applications has been found. If such
prior art exists, it may be used to invalidate a patent, or may prevent a patent from issuing from a pending patent application. For
example, such patent filings may be subject to a third-party submission of prior art to the USPTO, or to other patent offices around
the world. Alternately or additionally, we may become involved in post-grant review procedures, oppositions, derivation proceedings,
ex parte reexaminations, inter parties review, supplemental examinations, or interference proceedings or challenges in district court,
in the United States or in various foreign patent offices, including both national and regional, challenging patents or patent applications
in which we have rights, including patents on which we rely to protect our business. An adverse determination in any such challenges
may result in loss of the patent or in patent claims being narrowed, invalidated or held unenforceable, in whole or in part, or in denial
of the patent application or loss or reduction in the scope of one or more claims of the patent application, any of which could limit
our ability to stop others from using or commercializing similar or identical technology and products, or limit the duration of the patent
protection of our technology and products. In addition, given the amount of time required for the development, testing and regulatory
review of new product candidates, patents protecting such candidates might expire before or shortly after such candidates are commercialized.
Issued
patents that we have or may obtain or license may not provide us with any meaningful protection, prevent competitors from competing with
us or otherwise provide us with any competitive advantage. Our competitors may be able to circumvent our patents by developing similar
or alternative technologies or products in a non-infringing manner. Our competitors may also seek approval to market their own products
similar to or otherwise competitive with our products. Alternatively, our competitors may seek to market generic versions of any approved
products or pursue similar strategies in the United States or other jurisdictions, in which they claim that patents owned or licensed
by us are invalid, unenforceable or not infringed. In these circumstances, we may need to defend or assert our patents, or both, including
by filing lawsuits alleging patent infringement. In any of these types of proceedings, a court or other agency with jurisdiction may
find our patents invalid or unenforceable, or that our competitors are competing in a non-infringing manner. Thus, even if we have valid
and enforceable patents, these patents still may not provide protection against competing products or processes sufficient to achieve
our business objectives. Any of the foregoing could have a material adverse effect on our business, financial condition, results of operations
and prospects.
Other
parties have developed or may develop technologies that may be related to or competitive with our approach, and may have filed or may
file patent applications and may have been issued or may be issued patents with claims that overlap or conflict with our patent applications,
either by claiming the same materials, formulations or methods, or by claiming subject matter that could dominate our patent position.
In addition, certain parts or all of the patent portfolios licensed to us are, or may be, licensed to third parties and such third parties
may have or may obtain certain enforcement rights. If the scope of the patent protection we or our licensors obtain is not sufficiently
broad, we may not be able to prevent others from developing and commercializing technology and products similar or identical to ours.
The degree of patent protection we require to successfully compete in the marketplace may be unavailable or severely limited in some
cases and may not adequately protect our rights or permit us to gain or keep any competitive advantage. We cannot provide any assurances
that any of our licensed patents have, or that any of our pending owned or licensed patent applications that mature into issued patents
will include, claims with a scope sufficient to protect our product candidates or otherwise provide any competitive advantage, nor can
we provide any assurance that our licenses will remain in force.
In
addition, there are situations in which noncompliance can result in abandonment or lapse of the patent or patent application, resulting
in partial or complete loss of patent rights in the relevant jurisdiction. Noncompliance events that could result in abandonment or lapse
of a patent or patent application include, but are not limited to, failure to respond to official actions within prescribed time limits,
non-payment of fees and failure to properly legalize and submit formal documents.
If
we are unable to protect the confidentiality of our trade secrets, our business and competitive position may be harmed.
In
addition to the protection afforded by patents, we rely upon trade secret protection, know-how and continuing technological innovation
to develop and maintain our competitive position. We seek to protect our proprietary technology and processes, in part, by entering into
confidentiality agreements with our contractors, collaborators, scientific advisors, employees and consultants and invention assignment
agreements with our consultants and employees. However, we may not obtain these agreements in all circumstances, and individuals with
whom we have these agreements may not comply with their terms. The assignment of intellectual property rights under these agreements
may not be self-executing or the assignment agreements may be breached, and we may be forced to bring claims against third parties, or
defend claims that they may bring against us, to determine the ownership of what we regard as our intellectual property. In addition,
we may not be able to prevent the unauthorized disclosure or use of our technical know-how or other trade secrets by the parties to these
agreements despite the existence of confidentiality agreements and other contractual restrictions. Monitoring unauthorized uses and disclosures
is difficult and we do not know whether the steps we have taken to protect our proprietary technologies will be effective. If any of
the contractors, collaborators, scientific advisors, employees and consultants who are parties to these agreements breaches or violates
the terms of any of these agreements, we may not have adequate remedies for any such breach or violation. As a result, we could lose
our trade secrets. Enforcing a claim against a third party that illegally obtained and is using our trade secrets, like patent litigation,
is expensive and time-consuming and the outcome is unpredictable. In addition, courts outside the United States are sometimes less
willing or unwilling to protect trade secrets. Any of the foregoing could have a material adverse effect on our business, financial condition,
results of operations, and prospects.
Moreover,
our trade secrets could otherwise become known or be independently discovered by our competitors or other third parties. Competitors
and other third parties could attempt to replicate some or all of the competitive advantages we derive from our development efforts,
willfully infringe our intellectual property rights, design around our protected technology or develop their own competitive technologies
that fall outside of our intellectual property rights. If any of our trade secrets were to be lawfully obtained or independently developed
by a competitor or other third party, we would have no right to prevent them, or those to whom they communicate it, from using that technology
or information to compete with us. If our trade secrets are not adequately protected or sufficient to provide an advantage over our competitors,
our competitive position could be adversely affected, as could our business. Additionally, if the steps taken to maintain our trade secrets
are deemed inadequate, we may have insufficient recourse against third parties for misappropriating our trade secrets.
If
our trademarks and trade names are not adequately protected, then we may not be able to build name recognition in our markets of interest
and our business may be adversely affected.
Our
current or future trademarks or trade names may be challenged, infringed, circumvented or declared generic or descriptive or determined
to be infringing on other marks. We may not be able to protect our rights to these trademarks and trade names or may be forced to stop
using these names, which we need for name recognition by potential partners or customers in our markets of interest. Our company name
and logo, as well as our product candidate names “JSP191” and “JSP502”, are not registered trademarks. If we
seek to register any of our trademarks, during trademark registration proceedings, we may receive rejections of our applications by the
USPTO or in other foreign jurisdictions. Although we would be given an opportunity to respond to those rejections, we may be unable to
overcome such rejections. In addition, in the USPTO and in comparable agencies in many foreign jurisdictions, third parties are given
an opportunity to oppose pending trademark applications and to seek to cancel registered trademarks. Opposition or cancellation proceedings
may be filed against our trademarks, and our trademarks may not survive such proceedings. If we are unable to establish name recognition
based on our trademarks and trade names, we may not be able to compete effectively and our business may be adversely affected. We may
license our trademarks and trade names to third parties, such as distributors. Although these license agreements may provide guidelines
for how our trademarks and trade names may be used, a breach of these agreements or misuse of our trademarks and tradenames by our licensees
may jeopardize our rights in or diminish the goodwill associated with our trademarks and trade names.
Moreover,
any name we have proposed to use with our product candidate in the United States must be approved by the FDA, regardless of whether
we have registered it, or applied to register it, as a trademark. Similar requirements exist in Europe. The FDA typically conducts a
review of proposed product names, including an evaluation of potential for confusion with other product names. If the FDA (or an equivalent
administrative body in a foreign jurisdiction) objects to any of our proposed proprietary product names, we may be required to expend
significant additional resources in an effort to identify a suitable substitute name that would qualify under applicable trademark laws,
not infringe the existing rights of third parties and be acceptable to the FDA. Furthermore, in many countries, owning and maintaining
a trademark registration may not provide an adequate defense against a subsequent infringement claim asserted by the owner of a senior
trademark. At times, competitors or other third parties may adopt trade names or trademarks similar to ours, thereby impeding our ability
to build brand identity and possibly leading to market confusion. In addition, there could be potential trade name or trademark infringement
claims brought by owners of other registered trademarks or trademarks that incorporate variations of our registered or unregistered trademarks or
trade names. If we assert trademark infringement claims, a court may determine that the marks we have asserted are invalid or unenforceable,
or that the party against whom we have asserted trademark infringement has superior rights to the marks in question. In this case, we
could ultimately be forced to cease use of such trademarks.
We
may not be successful in acquiring or in-licensing necessary rights to key technologies underlying JSP191 or any future product candidates
we may develop.
We
currently have rights to intellectual property, through licenses from third parties, to develop JSP191, and we expect to seek to expand
our intellectual property footprint related to our product candidate pipeline in part by in-licensing the rights to key technologies.
The future growth of our business will depend in part on our ability to in-license or otherwise acquire the rights to develop additional
product candidates and technologies. Although we have succeeded in licensing technologies from third-party licensors, including Amgen
Inc. and Stanford, in the past, we can give no assurance that we will be able to in-license or acquire the rights to other technologies
relevant to our product candidates from third parties on acceptable terms or at all.
In
order to market our product candidates, we may find it necessary or prudent to obtain licenses from such third-party intellectual property
holders. However, it may be unclear who owns the rights to intellectual property we wish to obtain, or we may be unable to secure such
licenses or otherwise acquire or in-license intellectual property rights from third parties that we identify as necessary for product
candidates we may develop and technology we employ. For example, we employ a range of genome engineering technologies that are owned
by third parties in our preclinical studies, as well as to manufacture the supply of eHSCs or other cell therapies used for clinical
trials and, if approved, for commercialization of our product candidates. We currently conduct our preclinical research and clinical
trials under 35 U.S.C. § 271(e)(1), which provides a safe harbor from patent infringement for uses of patented technology reasonably
related to the development and submission of information under a federal law which regulates the manufacture, use, or sale of drugs.
The
licensing or acquisition of third-party intellectual property rights is a highly competitive area, and other companies may pursue strategies
to license or acquire third-party intellectual property rights that we may consider attractive or necessary. Such companies may have
a competitive advantage over us, e.g., due to their size, capital resources and greater clinical development and commercialization capabilities.
In addition, companies that perceive us to be a competitor may be unwilling to assign or license rights to us. We also may be unable
to license or acquire third-party intellectual property rights on terms that would allow us to make an appropriate return on our investment
or at all. If we are unable to successfully obtain rights to required third-party intellectual property rights or maintain the existing
intellectual property rights we have, we may have to abandon development of the relevant program or product candidate, which could have
a material adverse effect on our business, financial condition, results of operations and prospects.
Even
if we were able to obtain such a license, it could be non-exclusive, thereby giving our competitors and other third parties access to
the same technologies licensed to us, and it could require us to make substantial licensing and royalty payments. If we are unable to
obtain a necessary license to a third-party patent on commercially reasonable terms, we may be unable to commercialize our product candidates
or such commercialization efforts may be significantly delayed, which could in turn significantly harm our business.
Third-party
claims of intellectual property infringement, misappropriation or other violations may prevent or delay our product discovery and development
efforts and have a material adverse effect on our business.
Our
commercial success depends in part on us avoiding infringement, misappropriation and other violations of the patents and proprietary
rights of third parties. There is a substantial amount of litigation involving patents and other intellectual property rights in the
biotechnology and pharmaceutical industries, as well as administrative proceedings for challenging patents, including interference and
reexamination proceedings before the USPTO or oppositions and other comparable proceedings in foreign jurisdictions. Recently, under
U.S. patent reform, new procedures including inter partes review and post grant review have been implemented. This reform
will bring uncertainty to the possibility of challenge to our patents in the future. Numerous U.S.-and foreign-issued patents and pending
patent applications, which are owned by third parties, exist in the fields in which we are developing our product candidates, and third
parties may allege they have patent rights encompassing our product candidates, technologies or methods. Third parties may assert that
we are employing their proprietary technology without authorization and may file patent infringement claims or lawsuits against us, and
if we are found to infringe such third-party patents, we may be required to pay damages, cease commercialization of the infringing technology
or obtain a license from such third parties, which may not be available on commercially reasonable terms or at all.
There
may be third-party patents with patent rights to materials, formulations, methods of manufacture or methods of treatment related to the
use or manufacture of our product candidates. Because patent applications can take many years to issue, there may be currently pending
patent applications which may later result in issued patents that our product candidates may infringe. In addition, third parties may
obtain patents in the future and claim that use of our technologies infringes upon these patents. Further, we or our licensors may fail
to identify even those relevant third-party patents that have issued or may incorrectly interpret the relevance, scope or expiration
of such patents. The scope of a patent claim is determined by an interpretation of the law, the written disclosure in a patent and the
patent’s prosecution history. Our interpretation of the relevance or scope of a patent or a pending application may be incorrect.
If any third-party patents were held by a court of competent jurisdiction to cover the manufacturing process of our product candidates,
materials used in or formed during the manufacturing process or any final product itself, the holders of any such patents may be able
to block our ability to commercialize the product candidate unless we obtained a license under the applicable patents, or until such
patents expire or they are finally determined to be held invalid or unenforceable. Similarly, if any third-party patent were held by
a court of competent jurisdiction to cover aspects of our materials, formulations or methods, including without limitation, combination
therapy or patient selection methods, the holders of any such patent may be able to block our ability to develop and commercialize the
product candidate unless we obtained a license or until such patent expires or is finally determined to be held invalid or unenforceable.
Parties
making claims against us may seek and obtain injunctive or other equitable relief, which could effectively block our ability to further
develop and commercialize our product candidates. Defense of these claims, regardless of their merit, would involve substantial litigation
expense and would involve a substantial diversion of employee resources from our business. We may not have sufficient resources to bring
these actions to a successful conclusion, which may result in significant cost and may impede our inability to pursue any affected products
or product candidates. There could also be public announcements of the results of hearings, motions or other interim proceedings or developments.
If securities analysts or investors perceive these results to be negative, it could have a material adverse effect on the price of shares
of our common stock.
In
the event of a successful claim of infringement against us, we may have to pay substantial damages, including treble damages and attorneys’
fees for willful infringement, obtain one or more licenses from third parties, pay royalties or redesign our infringing products, which
may be impossible or require substantial time and monetary expenditure.
Some
intellectual property that we have in-licensed may have been discovered through government-funded programs and thus may be subject to
federal regulations such as “march-in” rights, certain reporting requirements and a preference for U.S.-based companies.
Compliance with such regulations may limit our exclusive rights and limit our ability to contract with non-U.S. manufacturers.
Any
of the intellectual property rights that we have licensed or may license in the future and that have been generated through the use of
U.S. government funding are subject to certain federal regulations. As a result, the U.S. government may have certain rights
to intellectual property embodied in our current or future product candidates pursuant to the Bayh-Dole Act of 1980 (“Bayh-Dole
Act”). These U.S. government rights in certain inventions developed under a government-funded program include a non-exclusive,
non-transferable, irrevocable worldwide license to use inventions for any governmental purpose. In addition, the U.S. government
would have the right to require us to grant exclusive, partially exclusive, or non-exclusive licenses to any such intellectual property
rights to a third party if it determines that:
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adequate steps have not been
taken to commercialize the invention; |
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government action is necessary
to meet public health or safety needs; or |
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government action is necessary
to meet requirements for public use under federal regulations (also referred to as “march-in rights”). |
The
U.S. government also has the right to take title to such intellectual property rights if we, or the applicable licensor, fail to
disclose the invention to the government and fail to file an application to register the intellectual property within specified time
limits. Intellectual property generated under a government-funded program is also subject to certain reporting requirements, compliance
with which may require us or the applicable licensor to expend substantial resources. We cannot be certain that our current or future
licensors will comply with the disclosure or reporting requirements of the Bayh-Dole Act at all times, or be able to rectify any lapse
in compliance with these requirements.
In
addition, the U.S. government requires that any products embodying the subject invention or produced through the use of the subject
invention be manufactured substantially in the United States. The manufacturing preference requirement can be waived if the owner
of the intellectual property can show that reasonable but unsuccessful efforts have been made to grant licenses on similar terms to potential
licensees that would be likely to manufacture substantially in the United States or that under the circumstances domestic manufacture
is not commercially feasible. This preference for U.S. manufacturers may limit our ability to contract with non-U.S. product
manufacturers for products covered by such intellectual property. To the extent any of our current or future intellectual property is
generated through the use of U.S. government funding, the provisions of the Bayh-Dole Act may similarly apply.
We
may become involved in lawsuits to protect or enforce our patents or other intellectual property, which could be expensive, time-consuming
and unsuccessful.
Competitors
may infringe our patents, trademarks, copyrights or other intellectual property. To counter infringement or unauthorized use, we may
be required to file infringement claims, which can be expensive and time-consuming and divert the time and attention of our management
and scientific personnel. Any claims we assert against perceived infringers could provoke these parties to assert counterclaims against
us alleging that we infringe their patents, in addition to counterclaims asserting that our patents are invalid or unenforceable, or
both. In any patent infringement proceeding, there is a risk that a court will decide that a patent of ours is invalid or unenforceable,
in whole or in part, and that we do not have the right to stop the other party from using the invention at issue. There is also a risk
that, even if the validity of such patents is upheld, the court will construe the patent’s claims narrowly or decide that we do
not have the right to stop the other party from using the invention at issue on the grounds that our patent claims do not cover the invention.
An adverse outcome in a litigation or proceeding involving our patents could limit our ability to assert our patents against those parties
or other competitors, and may curtail or preclude our ability to exclude third parties from making and selling similar or competitive
products. Any of these occurrences could adversely affect our competitive business position, business prospects and financial condition.
Similarly, if we assert trademark infringement claims, a court may determine that the marks we have asserted are invalid or unenforceable,
or that the party against whom we have asserted trademark infringement has superior rights to the marks in question. In this case, we
could ultimately be forced to cease use of such trademarks.
Even
if we establish infringement, the court may decide not to grant an injunction against further infringing activity and instead award only
monetary damages, which may or may not be an adequate remedy. Furthermore, because of the substantial amount of discovery required in
connection with intellectual property litigation, there is a risk that some of our confidential information could be compromised by disclosure
during litigation. There could also be public announcements of the results of hearings, motions or other interim proceedings or developments.
If securities analysts or investors perceive these results to be negative, it could have a material adverse effect on the price of shares
of our common stock. Moreover, there can be no assurance that we will have sufficient financial or other resources to file and pursue
such infringement claims, which typically last for years before they are concluded. Even if we ultimately prevail in such claims,
the monetary cost of such litigation and the diversion of the attention of our management and scientific personnel could outweigh any
benefit we receive as a result of the proceedings. Any of the foregoing may have a material adverse effect on our business, financial
condition, results of operations and prospects.
We
may not be able to protect our intellectual property rights throughout the world.
Filing,
prosecuting, maintaining, defending and enforcing patents on our product candidates in all countries throughout the world would be prohibitively
expensive, and our intellectual property rights in some countries outside the United States can be less extensive than those in
the United States. In addition, the laws of some foreign countries do not protect intellectual property rights to the same extent
as federal and state laws in the United States. Consequently, we may not be able to prevent third parties from practicing our inventions
in all countries outside the United States, or from selling or importing products made using our inventions in and into the United States
or other jurisdictions. Competitors may use our technologies in jurisdictions where we have not obtained patent protection to develop
their own drugs and may export otherwise infringing drugs to territories where we have patent protection, but enforcement rights are
not as strong as those in the United States. These drugs may compete with our product candidates and our patents or other intellectual
property rights may not be effective or sufficient to prevent them from competing.
Many
companies have encountered significant problems in protecting and defending intellectual property rights in foreign jurisdictions. The
legal systems of some countries do not favor the enforcement of patents and other intellectual property protection, which could make
it difficult for us to stop the infringement of our patents generally. Proceedings to enforce our patent rights in foreign jurisdictions
could result in substantial costs and divert our efforts and attention from other aspects of our business, could put our patents at risk
of being invalidated or interpreted narrowly and our patent applications at risk of not issuing and could provoke third parties to assert
claims against us. We may not prevail in any lawsuits that we initiate, and the damages or other remedies awarded, if any, may not be
commercially meaningful.
Many
countries have compulsory licensing laws under which a patent owner may be compelled under specified circumstances to grant licenses
to third parties. In addition, many countries limit the enforceability of patents against government agencies or government contractors.
In those countries, we may have limited remedies if patents are infringed or if we are compelled to grant a license to a third party,
which could materially diminish the value of those patents. This could limit our potential revenue opportunities. Accordingly, our efforts
to enforce our intellectual property rights around the world may be inadequate to obtain a significant commercial advantage from the
intellectual property that we develop or license, which could adversely affect our business, financial condition, results of operations,
and prospects.
If
we do not obtain patent term extension (PTE) and data exclusivity for JSP191 or any other product candidates we may develop, our
business may be materially harmed.
Depending
upon the timing, duration and conditions of any FDA marketing approval of our product candidates, one or more of our U.S. patents
may be eligible for limited patent term extension under the Drug Price Competition and Patent Term Restoration Act of 1984,
referred to as the Hatch-Waxman Amendments, and similar legislation in the European Union. The Hatch-Waxman Amendments permit a patent
term extension of up to five years for a patent covering an approved product as compensation for effective patent term lost during
product development and the FDA regulatory review process. However, we may not receive an extension if we fail to exercise due diligence
during the testing phase or regulatory review process, fail to apply within applicable deadlines, fail to apply prior to expiration of
relevant patents or otherwise fail to satisfy applicable requirements. Moreover, the length of the extension could be less than we request.
Only one patent per approved product can be extended; the extension cannot extend the total patent term beyond 14 years from
approval; and only those claims covering the approved drug, a method for using it or a method for manufacturing it may be extended. If
we are unable to obtain patent term extension or the term of any such extension is less than we request, the period during which we can
enforce our patent rights for the applicable product candidate will be shortened, and our competitors may obtain approval to market competing
products sooner. As a result, our revenue from applicable products could be reduced. Further, if this occurs, our competitors may take
advantage of our investment in development and trials by referencing our clinical and preclinical data and launch their product earlier
than might otherwise be the case, and our competitive position, business, financial condition, results of operations, and prospects could
be materially harmed.
Third
parties may assert that our employees or consultants have wrongfully used or disclosed confidential information or misappropriated trade
secrets.
We
employ individuals who were previously employed at universities or other biopharmaceutical companies, including our competitors or potential
competitors. Although we try to ensure that our employees and consultants do not use the proprietary information or know-how of others
in their work for us, we may be subject to claims that we or our employees, consultants or independent contractors have inadvertently
or otherwise used or disclosed intellectual property, including trade secrets or other proprietary information, of a former employer
or other third parties. We may also be subject to claims that patents and applications that we may file to protect inventions of our
employees or consultants are rightfully owned by their former employers or other third parties. Litigation may be necessary to defend
against these claims. If we fail in defending any such claims, in addition to paying monetary damages, we may lose valuable intellectual
property rights or personnel. Even if we are successful in defending against such claims, litigation could result in substantial costs
and be a distraction to management and other employees. Any of the foregoing would harm our business, financial condition, results of
operations, and prospects.
Risks
Related to Other Legal Compliance Matters
If
any of our product candidates are approved, an unfavorable reimbursement determination in any of the major markets could have a negative
impact on us. Further, an unfavorable change in such regimes (e.g., price controls) could have a negative impact on us.
The
regulations that govern marketing approvals, pricing, and reimbursement for new medicines vary widely from country to country. In the
U.S., recently enacted legislation may significantly change the approval requirements in ways that could involve additional costs and
cause delays in obtaining approvals. Some countries require approval of the sale price of a medicine before it can be marketed. In many
countries, the pricing review period begins after marketing or product licensing approval is granted. In some foreign markets, prescription
pharmaceutical pricing remains subject to continuing governmental control even after initial approval is granted. As a result, we might
obtain marketing approval for a medicine in a particular country, but then be subject to price regulations that delay our commercial
launch of the medicine, possibly for lengthy time periods, and negatively impact the revenues we are able to generate from the sale of
the medicine in that country. Adverse pricing limitations may hinder our ability to recoup our investment in one or more product candidates,
even if any product candidates we may develop obtain marketing approval.
Our
ability to commercialize any medicines successfully also will depend in part on the extent to which reimbursement for these medicines
and related treatments will be available from government health administration authorities, private health insurers, and other organizations.
Government authorities and third-party payors, such as private health insurers and health maintenance organizations, decide which medications
they will pay for and establish reimbursement levels. A primary trend in the U.S. healthcare industry and elsewhere is cost containment.
Government authorities and third-party payors have attempted to control costs by limiting coverage and the amount of reimbursement for
particular medications. For example, in May 2019, the Centers for Medicare & Medicaid Services (“CMS”) issued
a final rule to allow Medicare Advantage Plans the option of using step therapy, a type of prior authorization for Medicare Party B drugs,
beginning January 1, 2020. This final rule codified CMS’s policy change that was effective January 1, 2019.
Congress
and the Biden administration have each indicated that it will continue to seek new legislative and/or administrative measures to control
drug costs. Individual states in the U.S. have also increasingly passed legislation and implemented regulations designed to control
pharmaceutical product pricing, including price or patient reimbursement constraints, discounts, restrictions on certain product access
and marketing cost disclosure and transparency measures, and, in some cases, designed to encourage importation from other countries and
bulk purchasing.
At
the state level, legislatures have become increasingly aggressive in passing legislation and implementing regulations designed to control
pharmaceutical and biological product pricing. Some of these measures include price or patient reimbursement constraints, discounts,
restrictions on certain product access, marketing cost disclosure and transparency measures, and, in some cases, measures designed to
encourage importation from other countries and bulk purchasing. In addition, regional health care authorities and individual hospitals
are increasingly using bidding procedures to determine what pharmaceutical products and which suppliers will be included in their prescription
drug and other health care programs. Also, increasingly, third-party payors are requiring that drug companies provide them with predetermined
discounts from list prices and are challenging the prices charged for medical products. We cannot be sure that reimbursement will be
available for any medicine that we commercialize and, if reimbursement is available, the level of reimbursement. Reimbursement may impact
the demand for, or the price of, any product candidate for which we obtain marketing approval. If reimbursement is not available or is
available only to limited levels, we may not be able to successfully commercialize any product candidate for which we obtain marketing
approval.
There
may be significant delays in obtaining reimbursement for newly approved medicines, and coverage may be more limited than the purposes
for which the medicine is approved by the FDA or similar regulatory authorities outside the U.S. Moreover, eligibility for reimbursement
does not imply that any medicine will be paid for in all cases or at a rate that covers our costs, including research, development, manufacture,
sale and distribution. Interim reimbursement levels for new medicines, if applicable, may also not be sufficient to cover our costs and
may not be made permanent. Reimbursement rates may vary according to the use of the medicine and the clinical setting in which it is
used, may be based on reimbursement levels already set for lower cost medicines and may be incorporated into existing payments for other
services. Net prices for medicines may be reduced by mandatory discounts or rebates required by government healthcare programs or private
payors and by any future relaxation of laws that presently restrict imports of medicines from countries where they may be sold at lower
prices than in the U.S. Any such reductions could negatively impact our net product sales, if any of our product candidates are
ever approved.
Any
product candidate for which we obtain marketing approval could be subject to restrictions or withdrawal from the market, and we may be
subject to substantial penalties if we fail to comply with regulatory requirements or if we experience unanticipated problems with our
medicines, when and if any of them are approved.
The
FDA and other regulatory agencies closely regulate the post approval marketing and promotion of medicines to ensure that they are marketed
only for the approved indications and in accordance with the provisions of the approved labeling. The FDA and other regulatory agencies
impose stringent restrictions on manufacturers’ communications regarding off label use, and if we do not market our medicines for
their approved indications, we may be subject to enforcement action for off label marketing by the FDA and other federal and state enforcement
agencies, including the Department of Justice. Violation of the Federal Food, Drug, and Cosmetic Act and other statutes, including the
False Claims Act, relating to the promotion and advertising of prescription products may also lead to investigations or allegations of
violations of federal and state healthcare fraud and abuse laws and state consumer protection laws.
In
addition, later discovery of previously unknown problems with our medicines, third-party manufacturers, or manufacturing processes, or
failure to comply with regulatory requirements, may yield various results, including:
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restrictions on such medicines,
manufacturers, or manufacturing processes; |
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restrictions on the labeling
or marketing of a medicine; |
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restrictions on the distribution
or use of a medicine; |
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requirements to conduct post
marketing clinical trials; |
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receipt of warning or untitled
letters; |
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withdrawal of the medicines
from the market; |
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refusal to approve pending
applications or supplements to approved applications that we submit; |
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fines, restitution, or disgorgement
of profits or revenue; |
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suspension or withdrawal of
marketing approvals; |
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suspension of any ongoing clinical
trials; |
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refusal to permit the import
or export of our medicines; |
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injunctions or the imposition
of civil or criminal penalties. |
Any
government investigation of alleged violations of law could require us to expend significant time and resources in response and could
generate negative publicity. The occurrence of any event or penalty described above may inhibit our ability to commercialize any product
candidates we develop and adversely affect our business, financial condition, results of operations, and prospects.
Additionally,
if any of our product candidates receives marketing approval, the FDA could require it to adopt a Risk Evaluation and Mitigation Strategy,
to ensure that the benefits outweigh its risks, which may include, among other things, a medication guide outlining the risks of the
product for distribution to patients and a communication plan to healthcare practitioners. Furthermore, if we or others later identify
undesirable side effects caused by any of our product candidates, several potentially significant negative consequences could result,
including:
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regulatory authorities may
suspend or withdraw approvals of such product candidate; |
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regulatory authorities may
require additional warnings on the label; |
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we may be required to change
the way such product candidate is administered or conduct additional clinical trials; |
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we could be sued and held liable
for harm caused to patients; and |
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our reputation
may suffer. |
Our
relationships with healthcare providers, including physicians, and third-party payors will be subject to applicable anti-kickback, fraud
and abuse, anti-bribery and other healthcare laws and regulations, which could expose us to criminal sanctions, civil penalties, contractual
damages, reputational harm and diminished profits and future earnings.
Healthcare
providers and third-party payors play a primary role in the recommendation and prescription of any product candidates for which we obtain
marketing approval. Our current and future arrangements with healthcare providers, third-party payors and customers may expose us to
broadly applicable fraud and abuse and other healthcare laws and regulations that may constrain the business or financial arrangements
and relationships through which we research as well as market, sell and distribute our products for which we obtain marketing approval.
Restrictions under applicable federal and state healthcare laws and regulations, including certain laws and regulations applicable only
if we have marketed products, include, but are not limited to, the following:
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the federal healthcare program
Anti-Kickback Statute, which prohibits, among other things, persons or entities from knowingly and willfully soliciting, receiving,
offering, or providing any remuneration (including any kickback, bribe or certain rebates), directly or indirectly, in cash or in
kind, to induce, or in return for, either the referral of an individual, for the purchase, lease, order or recommendation of any
item, good, facility or service for which payment may be made, in whole or in part, under federal healthcare programs, such as Medicare
and Medicaid. A person or entity does not need to have actual knowledge of the statute or specific intent to violate it in order
to have committed a violation; |
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federal false claims, including
the False Claims Act that can be enforced through whistleblower actions, false statements and civil monetary penalties laws, which
prohibit, among other things, any person or entity from knowingly presenting, or causing to be presented, a false or fraudulent claim
for payment of government funds or knowingly making, or causing to be made, a false record or statement material to a false or fraudulent
claim to get a false claim paid or to avoid, decrease or conceal an obligation to pay money to the federal government. In addition,
the government may assert that a claim including items and services resulting from a violation of the U.S. federal Anti-Kickback
Statute constitutes a false or fraudulent claim for purposes of the False Claims Act; |
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the federal Health Insurance
Portability and Accountability Act of 1996 (“HIPAA”), which, prohibits, among other things, executing, or attempting
to execute, a scheme to defraud any healthcare benefit program or making false, fictitious, or fraudulent statements in connection
with the delivery of, or payment for, healthcare benefits, items or services relating to healthcare matters. Similar to the federal
Anti-Kickback Statute, a person or entity does not need to have actual knowledge of the statute or specific intent to violate it
in order to have committed a violation; |
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the federal false statements
statute, which prohibits knowingly and willfully falsifying, concealing, or covering up a material fact or making any materially
false statement in connection with the delivery of or payment for healthcare benefits, items, or services; |
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the federal Food, Drug, and
Cosmetic Act, which among other things, strictly regulates drug marketing, prohibits manufacturers from marketing such products for
off-label use and regulates the distribution of samples; |
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federal laws that require pharmaceutical
manufacturers to report certain calculated product prices to the government or provide certain discounts or rebates to government
authorities or private entities, often as a condition of reimbursement under government healthcare programs; |
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the federal Physician Payments
Sunshine Act, which requires certain manufacturers of drugs, devices, biologics and medical supplies for which payment is available
under Medicare, Medicaid or the Children’s Health Insurance Program (with certain exceptions) to report annually to the CMS
within the U.S. Department of Health and Human Services, information related to payments or other transfers of value made during
the previous year to physicians, (defined to include doctors, dentists, optometrists, podiatrists and chiropractors) and teaching
hospitals, as well as ownership and investment interests held by physicians and their immediate family members. Beginning in 2022,
such obligations include payments and other transfers of value provided in the previous year to certain other healthcare professionals,
including physician assistants, nurse practitioners, clinical nurse specialists, certified nurse anesthetists, anesthesiologist assistants
and certified nurse midwives; and |
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analogous state and foreign
laws and regulations, such as state anti-kickback and false claims laws, which may be broader in scope and apply to healthcare items
or services that are reimbursed by non-governmental third-party payors, including private insurers. |
Some
state laws also require pharmaceutical companies to comply with specific compliance standards, restrict financial interactions between
pharmaceutical companies and healthcare providers or require pharmaceutical companies to report information related to payments to health
care providers or marketing expenditures. Certain state laws also require the reporting of information related to drug pricing. Further,
certain state and local laws require the registration of pharmaceutical sales representatives.
Efforts
to ensure that our business arrangements with third parties will comply with applicable healthcare laws and regulations will involve
substantial costs. Given the breadth of the laws and regulations and evolving government interpretations of the laws and regulations,
governmental authorities may possibly conclude that our business practices, including certain of our advisory board arrangements with
physicians, some of whom are compensated in the form of stock or stock options, may not comply with healthcare laws and regulations.
If our operations are found to be in violation of any of the laws described above or any other government regulations that apply to us,
we may be subject to significant penalties, including administrative, civil and criminal penalties, damages, fines, disgorgement, exclusion
from participation in government health care programs, such as Medicare and Medicaid, imprisonment, integrity oversight and reporting
obligations, contractual damages, reputational harm, diminished profits and future earnings, and the curtailment or restructuring of
our operations, any of which could adversely affect our business, financial condition, results of operations, and prospects.
The
European Union has strict laws governing the provision of benefits or advantages to healthcare professionals in order to induce or encourage
the prescription, recommendation, endorsement, purchase, supply, order or use of medicinal products. Such laws and associated codes of
practice set out the rules and requirements that the provision of hospitality, sponsorship, gifts and promotional items must meet before
they can be accepted by healthcare professionals. The provision of benefits or advantages to healthcare professionals is also governed
by the national anti-bribery laws of European Union Member States. Infringement of these laws could result in substantial fines and imprisonment.
Payments
made to healthcare professionals in certain European Union Member States may be publicly disclosed. Moreover, agreements with healthcare
professionals often must be the subject of prior notification and approval by the healthcare professionals’ employer, his or her
competent professional organization, and/or the regulatory authorities of the individual European Union Member States. These requirements
are provided in the national laws, industry codes, or professional codes of conduct applicable in the European Union Member States. Failure
to comply with these requirements could result in reputational risk, public reprimands, administrative penalties, fines or imprisonment.
Healthcare
and other reform legislation, may increase the difficulty and cost for us and any collaborators we may have to obtain marketing approval
of and commercialize JSP191 and any other product candidates we may develop and affect the prices we, or they, may obtain.
In
the United States and some foreign jurisdictions, there have been, and continue to be, ongoing efforts to implement legislative
and regulatory changes regarding the healthcare system. Such changes could prevent or delay marketing approval of JSP191 and any other
product candidates that we may develop, restrict or regulate post-approval activities and affect our ability to profitably sell any product
candidates for which we obtain marketing approval. Although we cannot predict what healthcare or other reform efforts will be successful,
such efforts may result in more rigorous coverage criteria, in additional downward pressure on the price that we, or our future collaborators,
may receive for any approved products or in other consequences that may adversely affect our ability to achieve or maintain profitability.
Within
the United States, the federal government and individual states have aggressively pursued healthcare reform, as evidenced by the
passing of the ACA and the ongoing efforts to modify or repeal that legislation. The ACA substantially changed the way healthcare is
financed by both governmental and private insurers and contains a number of provisions that affect coverage and reimbursement of drug
products and/or that could potentially reduce the demand for pharmaceutical products such as increasing drug rebates under state Medicaid
programs for brand name prescription drugs and extending those rebates to Medicaid managed care and assessing a fee on manufacturers
and importers of brand name prescription drugs reimbursed under certain government programs, including Medicare and Medicaid. Other aspects
of healthcare reform, such as expanded government enforcement authority and heightened standards that could increase compliance-related
costs, could also affect our business. There are, and may continue to be, judicial challenges, including review by the United States
Supreme Court. We cannot predict the ultimate content, timing or effect of any changes to the ACA or other federal and state reform efforts.
There is no assurance that federal or state healthcare reform will not adversely affect our future business and financial results, and
we cannot predict how future federal or state legislative, judicial or administrative changes relating to healthcare reform will affect
our business.
Federal
and state governments have shown significant interest in implementing cost-containment programs to limit the growth of government-paid
healthcare costs, including price controls, waivers from Medicaid drug rebate law requirements, restrictions on reimbursement and requirements
for substitution of generic products for branded prescription drugs. The private sector has also sought to control healthcare costs by
limiting coverage or reimbursement or requiring discounts and rebates on products. We are unable to predict what additional legislation,
regulations or policies, if any, relating to the healthcare industry or third party coverage and reimbursement may be enacted in the
future or what effect such legislation, regulations or policies would have on our business. Any cost containment measures could significantly
decrease the available coverage and the price we might establish for our potential products, which would have an adverse effect on our
net revenues and operating results.
Legislative
and regulatory proposals have been made to expand post-approval requirements and restrict sales and promotional activities for biotechnology
products. We cannot be sure whether additional legislative changes will be enacted, or whether FDA regulations, guidance or interpretations
for biological products will be changed, or what the impact of such changes on the marketing approvals of our product candidates, if
any, may be. In addition, increased scrutiny by the U.S. Congress of the FDA’s approval and decision-making processes may
significantly delay or prevent marketing approval, as well as subject us to more stringent product labeling and post-marketing testing
and other requirements.
The
prices of prescription pharmaceuticals in the United States and foreign jurisdictions are subject to considerable legislative and
executive actions and could impact the prices we obtain for our products, if and when licensed.
The
prices of prescription pharmaceuticals have also been the subject of considerable discussion in the United States. To date, there
have been several recent U.S. congressional inquiries and proposed and enacted state and federal legislation designed to, among
other things, bring more transparency to drug pricing, review the relationship between pricing and manufacturer patient programs, reduce
the costs of drugs under Medicare and reform government program reimbursement methodologies for products. To those ends, President Trump
issued several executive orders intended to lower the costs of prescription drug products. Certain of these orders are reflected in recently
promulgated regulations, including an interim final rule implementing President Trump’s most favored nation model, but such final
rule is currently subject to a nationwide preliminary injunction. It remains to be seen whether these orders and resulting regulations
will remain in force during the Biden Administration. Further, on September 24, 2020, the Trump Administration finalized a rulemaking
allowing states or certain other non-federal government entities to submit importation program proposals to the FDA for review and approval.
Applicants are required to demonstrate that their importation plans pose no additional risk to public health and safety and will result
in significant cost savings for consumers. The FDA has issued draft guidance that would allow manufacturers to import their own FDA-approved
drugs that are authorized for sale in other countries (multi-market approved products).
At
the state level, individual states are increasingly aggressive in passing legislation and implementing regulations designed to control
pharmaceutical and biological product pricing, including price or patient reimbursement constraints, discounts, restrictions on certain
product access and marketing cost disclosure and transparency measures, and, in some cases, designed to encourage importation from other
countries and bulk purchasing. In addition, regional health care organizations and individual hospitals are increasingly using bidding
procedures to determine what pharmaceutical products and which suppliers will be included in their prescription drug and other health
care programs. These measures could reduce the ultimate demand for our products, once approved, or put pressure on our product pricing.
We expect that additional state and federal healthcare reform measures will be adopted in the future, any of which could limit the amounts
that federal and state governments will pay for healthcare products and services, which could result in reduced demand for our product
candidates or additional pricing pressures.
In
the European Union, similar political, economic and regulatory developments may affect our ability to profitably commercialize our product
candidates, if approved. In markets outside of the United States and the European Union, reimbursement and healthcare payment systems
vary significantly by country, and many countries have instituted price ceilings on specific products and therapies. In some countries,
particularly the countries of the European Union, the pricing of prescription pharmaceuticals is subject to governmental control. In
these countries, pricing negotiations with governmental authorities can take considerable time after the receipt of marketing approval
for a product. To obtain reimbursement or pricing approval in some countries, we may be required to conduct a clinical trial that compares
the cost-effectiveness of our product candidates to other available therapies. If reimbursement of our products is unavailable or limited
in scope or amount, or if pricing is set at unsatisfactory levels, our business could be harmed, possibly materially.
Our
employees, principal investigators, consultants and commercial partners may engage in misconduct or other improper activities, including
non-compliance with regulatory standards and requirements and insider trading.
We
are exposed to the risk of fraud or other misconduct by our employees, consultants and commercial partners, and, if we commence clinical
trials, our principal investigators. Misconduct by these parties could include intentional failures to comply with FDA regulations or
the regulations applicable in the European Union and other jurisdictions, provide accurate information to the FDA, the EMA and other
regulatory authorities, comply with healthcare fraud and abuse laws and regulations in the United States and abroad, report financial
information or data accurately or disclose unauthorized activities to us. In particular, sales, marketing and business arrangements in
the healthcare industry are subject to extensive laws and regulations intended to prevent fraud, misconduct, kickbacks, self-dealing
and other abusive practices. These laws and regulations restrict or prohibit a wide range of pricing, discounting, marketing and promotion,
sales commission, customer incentive programs and other business arrangements. Such misconduct also could involve the improper use of
information obtained in the course of clinical trials or interactions with the FDA, the EMA or other regulatory authorities, which could
result in regulatory sanctions and cause serious harm to our reputation. We have adopted a code of conduct applicable to all of our employees,
but it is not always possible to identify and deter employee misconduct, and the precautions we take to detect and prevent this activity
may not be effective in controlling unknown or unmanaged risks or losses or in protecting us from government investigations or other
actions or lawsuits stemming from a failure to comply with these laws or regulations. If any such actions are instituted against us,
and we are not successful in defending ourselves or asserting our rights, those actions could have a significant impact on our business,
financial condition, results of operations and prospects, including the imposition of significant fines or other sanctions.
Laws
and regulations governing any international operations we may have in the future may preclude us from developing, manufacturing and selling
certain product candidates outside of the United States and require us to develop and implement costly compliance programs.
We
may be subject to numerous laws and regulations in each jurisdiction outside of the United States in which we may operate. The creation,
implementation and maintenance of international business practices compliance programs is costly and such programs are difficult to enforce,
particularly where reliance on third parties is required.
The
Foreign Corrupt Practices Act (the “FCPA”), prohibits any U.S. individual or business from paying, offering, authorizing
payment or offering of anything of value, directly or indirectly, to any foreign official, political party or candidate for the purpose
of influencing any act or decision of the foreign entity in order to assist the individual or business in obtaining or retaining business.
The FCPA also obligates companies whose securities are listed in the United States to comply with certain accounting provisions
requiring us to maintain books and records that accurately and fairly reflect all transactions of the corporation, including international
subsidiaries, and to devise and maintain an adequate system of internal accounting controls for international operations. The anti-bribery
provisions of the FCPA are enforced primarily by the Department of Justice. The SEC is involved with enforcement of the books and records
provisions of the FCPA.
Similarly,
the U.K. Bribery Act 2010 has extra-territorial effect for companies and individuals having a connection with the United Kingdom.
The U.K. Bribery Act prohibits inducements both to public officials and private individuals and organizations. Compliance with the
FCPA and the U.K. Bribery Act is expensive and difficult, particularly in countries in which corruption is a recognized problem.
In addition, the FCPA presents particular challenges in the pharmaceutical industry, because, in many countries, hospitals are operated
by the government, and doctors and other hospital employees are considered foreign officials. Certain payments to hospitals in connection
with clinical trials and other work have been deemed to be improper payments to government officials and have led to FCPA enforcement
actions.
Various
laws, regulations and executive orders also restrict the use and dissemination outside of the United States, or the sharing with
certain non-U.S. nationals, of information classified for national security purposes, as well as certain products and technical
data relating to those products. Our expansion outside of the United States has required, and will continue to require, us to dedicate
additional resources to comply with these laws, and these laws may preclude us from developing, manufacturing or selling certain product
candidates outside of the United States, which could limit our growth potential and increase our development costs. The failure
to comply with laws governing international business practices may result in substantial penalties, including suspension or debarment
from government contracting. Violation of the FCPA can result in significant civil and criminal penalties. Indictment alone under the
FCPA can lead to suspension of the right to do business with the U.S. government until the pending claims are resolved. Conviction
of a violation of the FCPA can result in long-term disqualification as a government contractor. The termination of a government contract
or relationship as a result of our failure to satisfy any of our obligations under laws governing international business practices would
have a negative impact on our operations and harm our reputation and ability to procure government contracts. The SEC also may suspend
or bar issuers from trading securities on U.S. exchanges for violations of the FCPA’s accounting provisions.
Compliance
with global privacy and data security requirements could result in additional costs and liabilities to us or inhibit our ability to collect
and process data globally, and the failure to comply with such requirements could subject us to significant fines and penalties, which
may have a material adverse effect on our business, financial condition and results of operations.
The
regulatory framework for the collection, use, safeguarding, sharing, transfer, and other processing of information worldwide is rapidly
evolving and is likely to remain uncertain for the foreseeable future. Globally, virtually every jurisdiction in which we operate has
established its own data security and privacy frameworks with which we must comply. For example, the collection, use, disclosure, transfer,
or other processing of personal data regarding individuals in the European Union, including personal health data, is subject to the EU
General Data Protection Regulation (the “GDPR”), which took effect across all member states of the European Economic Area
(the “EEA”) in May 2018. The GDPR is wide-ranging in scope and imposes numerous requirements on companies that process
personal data, including requirements relating to processing health and other sensitive data, obtaining consent of the individuals to
whom the personal data relates, providing information to individuals regarding data processing activities, implementing safeguards to
protect the security and confidentiality of personal data, providing notification of data breaches, and taking certain measures when
engaging third-party processors. The GDPR increases our obligations with respect to clinical trials conducted in the EEA by expanding
the definition of personal data to include coded data and requiring changes to informed consent practices and more detailed notices for
clinical trial subjects and investigators. In addition, the GDPR imposes strict rules on the transfer of personal data to countries outside
the European Union, including the United States, and, as a result, increases the scrutiny that clinical trial sites located in the
EEA should apply to transfers of personal data from such sites to countries that are considered to lack an adequate level of data protection,
such as the United States. The GDPR also permits data protection authorities to require destruction of improperly gathered or used
personal information and/or impose substantial fines for violations of the GDPR, which can be up to four percent of global revenues or
20 million Euros, whichever is greater, and it also confers a private right of action on data subjects and consumer associations
to lodge complaints with supervisory authorities, seek judicial remedies, and obtain compensation for damages resulting from violations
of the GDPR. In addition, the GDPR provides that European Union member states may make their own further laws and regulations limiting
the processing of personal data, including genetic, biometric or health data.
Similar
actions are either in place or under way in the United States. There are a broad variety of data protection laws that are applicable
to our activities, and a wide range of enforcement agencies at both the state and federal levels that can review companies for privacy
and data security concerns based on general consumer protection laws. The Federal Trade Commission and state Attorneys General all are
aggressive in reviewing privacy and data security protections for consumers. New laws also are being considered at both the state and
federal levels. For example, the California Consumer Privacy Act — which went into effect on January 1, 2020 — is
creating similar risks and obligations as those created by the GDPR, though the California Consumer Privacy Act does exempt certain information
collected as part of a clinical trial subject to the Federal Policy for the Protection of Human Subjects (the Common Rule). In March 2020,
the California State Attorney General proposed varying versions of companion draft regulations which are not yet finalized. Despite the
delay in adopting regulations, the California State Attorney General commenced enforcement actions against violators beginning July 1,
2020. In addition, a new California privacy law, the California Privacy Rights Act (the “CPRA”) was passed by California
voters on November 3, 2020. The CPRA will create additional obligations with respect to processing and storing personal information that
are scheduled to take effect on January 1, 2023 (with certain provisions having retroactive effect to January 1, 2022). Further, a new
Virginia privacy law, Virginia Consumer Data Protection Act, or VCDPA, was signed into law on March 2, 2021 and is also scheduled to
take effect on January 1, 2023, and the Colorado Privacy Act, or CPA, will take effect on July 1, 2023. The VCDPA and CPA will impose
many similar obligations regarding the processing and storing of personal information as the California Consumer Privacy Act and the
CPRA. Many other states are considering similar legislation. A broad range of legislative measures also have been introduced at the federal
level. Accordingly, failure to comply with federal and state laws (both those currently in effect and future legislation) regarding privacy
and security of personal information could expose us to fines and penalties under such laws. There also is the threat of consumer class
actions related to these laws and the overall protection of personal data. Even if we are not determined to have violated these laws,
government investigations into these issues typically require the expenditure of significant resources and generate negative publicity,
which could harm our reputation and business.
Given
the breadth and depth of changes in data protection obligations, preparing for and complying with these requirements is rigorous and
time intensive and requires significant resources and a review of our technologies, systems and practices, as well as those of any third-party
collaborators, service providers, contractors or consultants that process or transfer personal data collected in the European Union.
The GDPR and other changes in laws or regulations associated with the enhanced protection of certain types of sensitive data, such as
healthcare data or other personal information from our clinical trials, could require us to change our business practices and put in
place additional compliance mechanisms, may interrupt or delay our development, regulatory and commercialization activities and increase
our cost of doing business, and could lead to government enforcement actions, private litigation and significant fines and penalties
against us and could have a material adverse effect on our business, financial condition and results of operations.
We
and our partners may be subject to stringent privacy laws, information security laws, regulations, policies and contractual obligations
related to data privacy and security, and changes in such laws, regulations, policies or how they are interpreted or changes in contractual
obligations could adversely affect our business.
There
are numerous U.S. federal and state data privacy and protection laws and regulations that apply to the collection, transmission,
processing, storage and use of personally-identifying information, which among other things, impose certain requirements relating to
the privacy, security and transmission of personal information. The legislative and regulatory landscape for privacy and data protection
continues to evolve in jurisdictions worldwide, and there has been an increasing focus on privacy and data protection issues with the
potential to affect our business. Failure to comply with any of these laws and regulations could result in enforcement action against
us, including fines, imprisonment of company officials and public censure, claims for damages by affected individuals, damage to our
reputation and loss of goodwill, any of which could have a material adverse effect on our business, financial condition, results of operations
or prospects.
If
we are unable to properly protect the privacy and security of health-related information or other sensitive or confidential information
in our possession, we could be found to have breached our contracts. Further, if we fail to comply with applicable privacy laws, including
applicable HIPAA privacy and security standards, we could face significant administrative, civil and criminal penalties. Enforcement
activity can also result in financial liability and reputational harm, and responses to such enforcement activity can consume significant
internal resources. In addition, state attorneys general are authorized to bring civil actions seeking either injunctions or damages
in response to violations that threaten the privacy of state residents.
We are
subject to recently enacted state laws in California that require gender and diversity quotas for boards of directors of public
companies headquartered in California.
In
September 2018, California enacted Senator Bill 826 (“SB 826”), which generally requires public companies
with principal executive offices in California to have at least two female directors on its board of directors if the company has at
least five directors, and at least three female directors on its board of directors if the company has at least six directors.
Additionally,
on September 30, 2020, California enacted Assembly Bill 979 (“AB 979”), which generally requires public companies
with principal executive offices in California to include specified numbers of directors from “underrepresented communities”.
A director from an “underrepresented community” means a director who self-identifies as Black, African American, Hispanic,
Latino, Asian, Pacific Islander, Native American, Native Hawaiian, Alaska Native, gay, lesbian, bisexual or transgender. By December
31, 2021, each public company with principal executive offices in California was required to have at least one director from an underrepresented
community. By December 31, 2022, a public company with more than four but fewer than nine directors will be required to have a minimum
of two directors from underrepresented communities, and a public company with nine or more directors will need to have a minimum of three
directors from underrepresented communities.
We
cannot assure that we can recruit, attract and/or retain qualified members of the board and meet gender and diversity quotas as required
by with SB 826 or AB 979, and our board of directors does not currently satisfy the quota required under SB 826. A failure to comply
with either SB 826 or AB 979 could result in fines from the California Secretary of State, with a $100,000 fine for the first violation
and a $300,000 fine for each subsequent violation of either law, and our reputation may be adversely affected.
Risks
Related to Employee Matters, Managing Growth and Information Technology
If
we lose key management personnel, or if we fail to recruit additional highly skilled personnel, our ability to continue developing and
to identify and develop new or next generation product candidates will be impaired, which could result in delays in the development process,
loss of market opportunities, make us less competitive and have a material adverse effect on our business, financial condition and results
of operations.
Our
ability to compete in the highly competitive biotechnology and pharmaceutical industries depends upon our ability to attract and retain
highly qualified managerial, scientific and medical personnel. We are highly dependent on our management, particularly our Chief Executive
Officer, the members of our executive team, and key scientific and medical personnel employees. The loss of the services of any of our
executive officers, key employees, and scientific and medical advisors, and our inability to find suitable replacements, could result
in delays in product development and harm our business.
We
conduct our operations at our facility in the San Francisco Bay Area. This region is headquarters to many other biopharmaceutical companies
and many academic and research institutions. Competition for skilled personnel in our market is intense and may limit our ability to
hire and retain highly qualified personnel on acceptable terms or at all.
To
induce valuable employees to remain at our company, in addition to salary and cash incentives, we have provided stock options that vest
over time. The value to employees of stock options that vest over time may be significantly affected by movements in our stock price
that are beyond our control, and may at any time be insufficient to counteract more lucrative offers from other companies. Despite our
efforts to retain valuable employees, members of our management, scientific and development teams may terminate their employment with
us on short notice. In addition, we may experience employee turnover as a result of the ongoing “great resignation” occurring
throughout the U.S. economy, which has impacted job market dynamics. New hires require training and take time before they achieve full
productivity. New employees may not become as productive as we expect, and we may be unable to hire or retain sufficient numbers of qualified
individuals. Although we have employment agreements with our key employees, these agreements provide for at-will employment, which means
that any of our employees could leave our employment at any time, with or without notice. We do not maintain “key man” insurance
policies on the lives of these individuals or the lives of any of our other employees. Our success also depends on our ability to continue
to attract, retain and motivate highly skilled junior, mid-level and senior managers as well as junior, mid-level and senior scientific
and medical personnel.
We
and our management have a limited track record as an operating company. Failures in the operational execution of the expected business
plans may have a material impact on our commercial prospects. Further, if we are not able to attract and retain highly-qualified personnel,
we may not be able to successfully implement our business strategy.
Our
management team has worked together for only a limited period of time and has a limited track record of executing our business plan as
a team. In addition, we have recently filled a number of positions in our finance and accounting staff. Accordingly, certain key personnel
have only recently assumed the duties and responsibilities they are now performing, and it is difficult to predict whether our management
team, individually and collectively, will be effective in operating our business. These changes may cause speculation and uncertainty
regarding our commercial prospects and may cause or result in:
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disruption of our business
or distraction of our employees and management; |
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difficulty in recruiting, hiring,
motivating, and retaining talented and skilled personnel; |
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stock price volatility; and |
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difficulty in negotiating,
maintaining, or consummating business or strategic relationships or transactions. |
If
we are unable to mitigate these risks or to attract and retain highly qualified personnel, our revenue, operating results and financial
condition may be adversely impacted.
We
will need to grow the size of our organization, and we may experience difficulties in managing this growth.
As
of December 31, 2021, we had 25 full-time employees. As our development, manufacturing and commercialization plans and strategies
develop and we continue our operations as a public company, we expect to need and are actively recruiting additional managerial, operational,
sales, marketing, financial and other personnel. Future growth would impose significant added responsibilities on members of management,
including:
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identifying, recruiting, integrating,
maintaining and motivating additional employees; |
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● |
managing our internal development
efforts effectively, including the clinical, FDA and international regulatory review process for our product candidates, while complying
with our contractual obligations to contractors and other third parties; and |
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improving our operational,
financial and management controls, reporting systems and procedures. |
Our
future financial performance and our ability to commercialize our product candidates will depend, in part, on our ability to effectively
manage any future growth, and our management may also have to divert a disproportionate amount of time to managing these growth activities.
We
currently rely, and for the foreseeable future will continue to rely, in substantial part on certain independent organizations, advisors
and consultants to provide certain services, including substantially all aspects of regulatory approval, clinical management and manufacturing.
We cannot assure you that the services of independent organizations, advisors and consultants will continue to be available to us on
a timely basis when needed, or that we can find qualified replacements. In addition, if we are unable to effectively manage our outsourced
activities or if the quality or accuracy of the services provided by consultants is compromised for any reason, our clinical trials may
be extended, delayed or terminated, and we may not be able to obtain regulatory approval of our product candidates or otherwise advance
our business. We cannot assure you that we will be able to manage our existing consultants or find other competent outside contractors
and consultants on economically reasonable terms, or at all. If we are not able to effectively expand our organization by hiring new
employees and expanding our groups of consultants and contractors, or if we are not able to effectively build out new facilities to accommodate
this expansion, we may not be able to successfully implement the tasks necessary for further development and commercialization of our
product candidates and, accordingly, may not achieve our research, development and commercialization goals.
Our
insurance policies may be inadequate and potentially expose us to unrecoverable risks.
We
have limited director and officer insurance and commercial insurance policies. Any significant insurance claims would have a material
adverse effect on our business, financial condition and results of operations. Insurance availability, coverage terms and pricing continue
to vary with market conditions. We endeavor to obtain appropriate insurance coverage for insurable risks that we identify; however, we
may fail to correctly anticipate or quantify insurable risks; we may not be able to obtain appropriate insurance coverage; and insurers
may not respond as we intend to cover insurable events that may occur. We have observed rapidly changing conditions in the insurance
markets relating to nearly all areas of traditional corporate insurance. Such conditions have resulted in higher premium costs, higher
policy deductibles and lower coverage limits. For some risks, we may not have or maintain insurance coverage because of cost or availability.
Our
internal computer systems, or those of our third-party vendors, collaborators or other contractors or consultants, may fail or suffer
security breaches, which could result in a material disruption of our product development programs, compromise sensitive information
related to our business or prevent us from accessing critical information, potentially exposing us to liability or otherwise adversely
affecting our business.
Our
internal computer systems and those of our current and any future third-party vendors, collaborators and other contractors or consultants
are vulnerable to damage or interruption from computer viruses, computer hackers, malicious code, employee theft or misuse, denial-of-service
attacks, sophisticated nation-state and nation-state-supported actors, unauthorized access, natural disasters, terrorism, war and telecommunication
and electrical failures. While we seek to protect our information technology systems from system failure, accident and security breach,
if such an event were to occur and cause interruptions in our operations, it could result in a disruption of our development programs
and our business operations, whether due to a loss of our trade secrets or other proprietary information or other disruptions. For example,
the loss of clinical trial data from future clinical trials could result in delays in our regulatory approval efforts and significantly
increase our costs to recover or reproduce the data. If we were to experience a significant cybersecurity breach of our information systems
or data, the costs associated with the investigation, remediation and potential notification of the breach to counter-parties and data
subjects could be material. In addition, our remediation efforts may not be successful. If we do not allocate and effectively manage
the resources necessary to build and sustain the proper technology and cybersecurity infrastructure, we could suffer significant business
disruption, including transaction errors, supply chain or manufacturing interruptions, processing inefficiencies, data loss or the loss
of or damage to intellectual property or other proprietary information.
Although
we take such steps to help protect confidential and other sensitive information from unauthorized access or disclosure, our information
technology and infrastructure may be vulnerable to attacks by hackers or viruses, failures, or breaches due to third-party action, employee
negligence or error, malfeasance, or other incidents or disruptions. For example, we could be the target of phishing attacks seeking
confidential information regarding our employees. Furthermore, while we have implemented data privacy and security measures in an effort
to comply with applicable laws and regulations relating to privacy and data protection, some health-related and other personal information
or confidential information may be transmitted to us by third parties, who may not implement adequate security and privacy measures,
and it is possible that laws, rules and regulations relating to privacy, data protection, or information security may be interpreted
and applied in a manner that is inconsistent with our practices or those of third parties who transmit health-related and other personal
information or confidential information to us.
To
the extent that we or these third parties are found to have violated such laws, rules or regulations or that any disruption or security
breach were to result in a loss of, or damage to, us or our third-party vendors’, collaborators’ or other contractors’
or consultants’ data or applications, or inappropriate disclosure of confidential or proprietary information, we could incur liability
including litigation exposure, penalties and fines, we could become the subject of regulatory action or investigation, our competitive
position could be harmed and the further development and commercialization of our product candidates could be delayed. Any of the above
could have a material adverse effect on our business, financial condition, results of operations or prospects.
Unstable
market and economic conditions may have serious adverse consequences on our business, financial condition and share price.
As
widely reported, global credit and financial markets have experienced volatility and disruptions in the past several years and especially
in 2020 and 2021 due to the impacts of the COVID-19 pandemic, including severely diminished liquidity and credit availability, declines
in consumer confidence, declines in economic growth, increases in unemployment rates and uncertainty about economic stability. There
can be no assurances that further deterioration in credit and financial markets and confidence in economic conditions will not occur.
Our general business strategy may be adversely affected by any such economic downturn, volatile business environment or continued unpredictable
and unstable market conditions. If the current equity and credit markets deteriorate, it may make any necessary debt or equity financing
more difficult, more costly and more dilutive. Failure to secure any necessary financing in a timely manner and on favorable terms could
have a material adverse effect on our growth strategy, financial performance and share price and could require us to delay or abandon
clinical development plans.
Risks
Related to Ownership of Our Common Stock and Warrants
If
our operations and performance do not meet the expectations of investors or securities analysts or for other reasons, the market price
of our securities may decline.
Any
of the factors listed below could have a negative impact on your investment in our securities, and our securities may trade at prices
significantly below the price you paid for them. In such circumstances, the trading price of our securities may not recover and may experience
a further decline.
Factors
affecting the trading price of our securities may include:
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adverse regulatory decisions; |
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any delay in our regulatory
filings for our product candidates and any adverse development or perceived adverse development with respect to the applicable regulatory
authority’s review of such filings, including without limitation the FDA’s issuance of a “refusal to file”
letter or a request for additional information; |
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the impacts of the ongoing
COVID-19 pandemic and related restrictions; |
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the commencement, enrollment
or results of any future clinical trials we may conduct, or changes in the development status of our product candidates; |
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adverse results from, delays
in or termination of clinical trials; |
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unanticipated serious safety
concerns related to the use of our product candidates; |
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lower than expected market
acceptance of our product candidates following approval for commercialization; |
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changes in financial estimates
by us or by any securities analysts who might cover our stock; |
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changes in the market valuations
of similar companies; |
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stock market price and volume
fluctuations of comparable companies and, in particular, those that operate in the biopharmaceutical industry; |
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publication of research reports
about us or our industry or positive or negative recommendations or withdrawal of research coverage by securities analysts; |
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announcements by us or our
competitors of significant acquisitions, strategic partnerships or divestitures; |
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announcements of investigations
or regulatory scrutiny of our operations or lawsuits filed against us; |
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investors’ general perception
of our business or management; |
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recruitment or departure of
key personnel; |
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overall performance of the
equity markets; |
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disputes or other developments
relating to intellectual property rights, including patents, litigation matters and our ability to obtain, maintain, defend, protect
and enforce patent and other intellectual property rights for our technologies; |
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significant lawsuits, including
patent or stockholder litigation; |
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proposed changes to healthcare
laws in the U.S. or foreign jurisdictions, or speculation regarding such changes; |
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general political and economic
conditions; and |
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other events or factors, many
of which are beyond our control. |
In
addition, the stock market in general, Nasdaq and pharmaceutical companies in particular have experienced extreme price and volume fluctuations
that have often been unrelated or disproportionate to the operating performance of these companies. Broad market and industry factors
may negatively affect the market price of our securities, regardless of our actual operating performance. In the past, stockholders have
initiated class action lawsuits against pharmaceutical and biotechnology companies following periods of volatility in the market
prices of these companies’ stock. Such litigation, if instituted against us, could cause us to incur substantial costs and divert
management’s attention and resources from our business.
Insiders
have substantial control over us, which could limit your ability to affect the outcome of key transactions, including a change of control.
As of December 31, 2021, our directors and executive officers and their
affiliates beneficially owned approximately 36.9% of the outstanding shares of our common stock. As a result, these stockholders, if they
act together, will be able to influence our management and affairs and all matters requiring stockholder approval, including the election
of directors and approval of significant corporate transactions, such as a merger or other sale of our company or our assets. This concentration
of ownership may have the effect of delaying or preventing a change in control of our company or discouraging a potential acquirer from
making a tender offer or otherwise attempting to obtain control, even if that change in control would benefit our other stockholders.
This significant concentration of ownership may also adversely affect the trading price for our common stock because investors often perceive
disadvantages in owning stock in companies with controlling stockholders.
We
will incur significant increased expenses and administrative burdens as a public company, which could negatively impact our business,
financial condition and results of operations.
We
face increased legal, accounting, administrative and other costs and expenses as a public company that we did not incur as a private
company. The Sarbanes-Oxley Act, including the requirements of Section 404, as well as rules and regulations subsequently implemented
by the SEC, the Dodd-Frank Wall Street Reform and Consumer Protection Act of 2010 and the rules and regulations promulgated
and to be promulgated thereunder, and the securities exchanges, impose additional reporting and other obligations on public companies.
Compliance with public company requirements will increase costs and make certain activities more time-consuming. A number of those requirements
will require us to carry out activities we had not done previously. For example, we have adopted new charters for our board committees
and adopted some new disclosure controls and procedures. In addition, expenses associated with SEC reporting requirements will be incurred.
Furthermore, if any issues in complying with those requirements are identified (for example, if the auditors identify a material weakness
or significant deficiency in the internal control over financial reporting), we could incur additional costs rectifying those issues,
and the existence of those issues could adversely affect our reputation or investor perceptions of us. It may also be more expensive
to obtain director and officer liability insurance. Risks associated with our status as a public company may make it more difficult to
attract and retain qualified persons to serve on our board of directors or as executive officers. The additional reporting and other
obligations imposed by these rules and regulations will increase legal and financial compliance costs and the costs of related legal,
accounting and administrative activities. These increased costs will require us to divert a significant amount of money that could otherwise
be used to expand our business and achieve strategic objectives. Advocacy efforts by stockholders and third parties may also prompt additional
changes in governance and reporting requirements, which could further increase costs.
Our
failure to timely and effectively implement controls and procedures required by Section 404(a) of the Sarbanes-Oxley Act could
negatively impact our business.
Absent
an applicable exemption, we are required to provide a management’s attestation on internal controls over financial reporting, and
we were not previously required to do this as a private company. The standards required for a public company under Section 404(a) of
the Sarbanes-Oxley Act are significantly more stringent than those required of us when we were a privately held company. Management may
not be able to effectively and timely implement controls and procedures that adequately respond to the increased regulatory compliance
and reporting requirements. If we are not able to implement the additional requirements of Section 404(a) in a timely manner
or with adequate compliance, we may not be able to assess whether our internal controls over financial reporting are effective, which
may subject us to adverse regulatory consequences and could harm investor confidence and the market price of our securities.
We
are an “emerging growth company” within the meaning of the Securities Act, and if we take advantage of certain exemptions
from disclosure requirements available to emerging growth companies, it could make our securities less attractive to investors and may
make it more difficult to compare our performance to the performance of other public companies.
We
are an “emerging growth company” as defined in Section 2(a)(19) of the U.S. Securities Act of 1933, as amended
(the “Securities Act”), as modified by the JOBS Act. As such, we are eligible for and intend to take advantage of certain
exemptions from various reporting requirements applicable to other public companies that are not emerging growth companies for as long
as we continue to be an emerging growth company, including, but not limited to, (a) not being required to comply with the auditor
attestation requirements of Section 404 of the Sarbanes-Oxley Act, (b) reduced disclosure obligations regarding executive compensation
in our periodic reports and proxy statements and (c) exemptions from the requirements of holding a nonbinding advisory vote on executive
compensation and stockholder approval of any golden parachute payments not previously approved. As a result, our stockholders may not
have access to certain information they may deem important. We will remain an emerging growth company until the earlier of (i) the
last day of the fiscal year (a) following November 22, 2024, (b) in which we have total annual gross revenue of at least
$1.07 billion, or (c) in which we are deemed to be a large accelerated filer, which means the market value of our common equity
that is held by non-affiliates exceeds $700 million as of the last business day of our most recently completed second fiscal
quarter; and (ii) the date on which we have issued more than $1.00 billion in non-convertible debt securities during the prior
three-year period. We cannot predict whether investors will find our securities less attractive because we will rely on these exemptions.
If some investors find our securities less attractive as a result of our reliance on these exemptions, the trading prices of our securities
may be lower than they otherwise would be; there may be a less active trading market for our securities; and the trading prices of our
securities may be more volatile.
Further,
Section 102(b)(1) of the JOBS Act exempts emerging growth companies from being required to comply with new or revised financial
accounting standards until private companies (that is, those that have not had a Securities Act registration statement declared effective
or do not have a class of securities registered under the Exchange Act) are required to comply with the new or revised financial
accounting standards. The JOBS Act provides that a company can elect to opt out of the extended transition period and comply with the
requirements that apply to non-emerging growth companies but any such an election to opt out is irrevocable. We have opted to take advantage
of the exemption for complying with new or revised accounting standards within the same time periods as private companies, which means
that when a standard is issued or revised and it has different application dates for public or private companies, we, as an emerging
growth company, can adopt the new or revised standard at the time private companies adopt the new or revised standard. This may make
comparison of our consolidated financial statements with another public company that is neither an emerging growth company nor an emerging
growth company that has opted out of using the extended transition period difficult or impossible because of the potential differences
in accounting standards used.
Even
after we no longer qualify as an emerging growth company, we may still qualify as a “smaller reporting company,” which would
allow us to take advantage of many of the same exemptions from disclosure requirements, including reduced disclosure obligations regarding
executive compensation in our periodic reports and proxy statements. If we cease to be an emerging growth company and do not qualify
as a smaller reporting company, we will no longer be able to take advantage of certain exemptions from reporting discussed above, including
not being able to take advantage of extended transition periods for the adoption of new or modified accounting standards, and, absent
other exemptions or relief available from the SEC, we will also be required to comply with the auditor attestation requirements of Section 404
of the Sarbanes-Oxley Act if we are no longer a non-accelerated filer at such time. We will incur additional expenses in connection with
such compliance, and our management will need to devote additional time and effort to implement and comply with such requirements.
If
securities or industry analysts do not publish or cease publishing research or reports about us, our business, or our market, or if they
change their recommendations regarding our securities adversely, the price and trading volume of our securities could decline.
The
trading market for our common stock will be influenced by the research and reports that industry or financial analysts publish about
us or our business. Securities and industry analysts do not currently, and may never, publish research on us. If no or few analysts commence
coverage of us, the trading price of our securities would likely decrease. Even if we do obtain analyst coverage, if one or more of the
analysts covering our business downgrade their evaluations of our securities, the price of our securities could decline. If one or more
of these analysts cease to cover our securities, we could lose visibility in the market for our securities, which in turn could cause
the price of our securities to decline.
Future
sales, or the perception of future sales, by us or our stockholders in the public market, the issuance of rights to purchase our common
stock, including pursuant to the Equity Incentive Plan and the ESPP, and future exercises of registration rights could result in the
additional dilution of the percentage ownership of our stockholders and cause the market price for our common stock to decline.
The
sale of shares of our common stock, convertible securities or other equity securities in the public market, or the perception that such
sales could occur, could harm the prevailing market price of shares of our common stock. These sales, or the possibility that these sales
may occur, also might make it more difficult for us to sell equity securities in the future at a time and at a price that we deem appropriate.
In addition, if we sell shares of our common stock, convertible securities or other equity securities, investors may be materially diluted
by subsequent sales. Such sales may also result in material dilution to our existing stockholders, and new investors could gain rights,
preferences, and privileges senior to the holders of our common stock.
Pursuant to the Jasper Therapeutics, Inc. 2021
Equity Incentive Plan (the “Equity Incentive Plan”), which became effective on September 23, 2021, we are authorized
to grant equity awards to our employees, directors and consultants. In addition, pursuant to the Jasper Therapeutics, Inc. 2021 Employee
Stock Purchase Plan (the “ESPP”), which became effective on September 23, 2021, we are authorized to sell shares to
our employees. A total of up to 4,400,000 and up to 550,000 shares of our common stock were initially reserved for future issuance
under the Equity Incentive Plan and the ESPP, respectively. In addition, the Equity Incentive Plan and ESPP provide for annual automatic
increases in the number of shares reserved thereunder, in each case, beginning on January 1, 2022. On January 1, 2022, pursuant
to the foregoing provisions, 1,514,204 and 378,551 shares of common stock were added to the shares reserved for future issuance under
the Equity Incentive Plan and the ESPP, respectively. As a result of such annual increases, our stockholders may experience additional
dilution, which could cause the price of our common stock to fall.
As of December 31, 2021, options to purchase an aggregate
of 2,660,261 shares of our common stock were outstanding that were previously issued under the Jasper Therapeutics, Inc. 2019 Equity Incentive
Plan (the “2019 EIP”). We assumed the 2019 Plan in connection with the Business Combination and no further awards will be
granted under the 2019 EIP. However, shares of our common stock subject to outstanding awards granted under the 2019 EIP that (a) are
not issued because the award or any portion of the award expires or otherwise terminates without all of the shares covered by the award
having been issued, (b) are withheld or reacquired to satisfy the exercise, strike or purchase price or (c) are withheld or
reacquired to satisfy a tax withholding obligation will also be added to the number of shares of our common stock available for issuance
pursuant to the Equity Incentive Plan. As of December 31, 2021, a total of 22,480 shares of common stock had been added to the number
of shares of our common stock available for issuance pursuant to the Equity Incentive Plan as a result of the cancellation of certain
options previously granted under the 2019 EIP.
Pursuant
to the Amended and Restated Registration Rights Agreement entered into in connection with the Business Combination, certain of our stockholders
can demand that we register their registrable securities under certain circumstances and will each also have piggyback registration rights
for these securities. In addition, we are required to file and maintain an effective registration statement under the Securities Act
covering such securities and certain of our other securities. We filed a registration statement on October 18, 2021 in order to satisfy
the foregoing obligations and registered for resale an aggregate of 38,081,493 shares of our common stock, including up to 5,000,000
shares of our common stock issuable upon exercise of our outstanding warrants. The registration of these securities permits the public
sale of such securities, subject to certain contractual restrictions on transfer imposed by the Amended and Restated Registration Rights
Agreement and the Business Combination Agreement, which contractual restrictions on transfer will terminate on March 23, 2022. The presence
of these additional shares of our common stock trading in the public market may have an adverse effect on the market price of our securities.
In
the future, we may also issue our securities in connection with investments or acquisitions. The amount of shares of our common stock
issued in connection with an investment or acquisition could constitute a material portion of our then-outstanding shares of our common
stock. Any issuance of additional securities in connection with investments or acquisitions may result in additional dilution to our
stockholders.
Because
there are no current plans to pay cash dividends on our common stock for the foreseeable future, you may not receive any return on investment
unless you sell shares of our common stock for a price greater than that which you paid for it.
We
may retain future earnings, if any, for future operations, expansion and debt repayment and have no current plans to pay any cash dividends
for the foreseeable future. Any decision to declare and pay dividends as a public company in the future will be made at the discretion
of our board of directors and will depend on, among other things, our results of operations, financial condition, cash requirements,
contractual restrictions and other factors that our board of directors may deem relevant. In addition, our ability to pay dividends may
be limited by covenants of any existing and future outstanding indebtedness we or our subsidiaries incur. As a result, you may not receive
any return on an investment in our common stock unless you sell your shares of our common stock for a price greater than that which you
paid for it.
Anti-takeover
provisions in our Certificate of Incorporation and under Delaware law could make an acquisition of us, which may be beneficial to our
stockholders, more difficult and may prevent attempts by our stockholders to replace or remove our current management.
Our
Second Amended and Restated Certificate of Incorporation (our “Certificate of Incorporation”) contains provisions that could
delay or prevent a change of control of us or changes in our board of directors that our stockholders might consider favorable. Some
of these provisions include:
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a board of directors divided
into three classes serving staggered three-year terms, such that not all members of our board of directors will be elected at one
time; |
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a prohibition on stockholder
action through written consent, which requires that all stockholder actions be taken at a meeting of our stockholders; |
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a requirement that special
meetings of stockholders be called only by the chairman of our board of directors, the chief executive officer, the president, or
by a majority of the total number of authorized directors; |
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advance notice requirements
for stockholder proposals and nominations for election to our board of directors; |
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a requirement that no member
of our board of directors may be removed from office by our stockholders except for cause and, in addition to any other vote required
by law, upon the approval of not less than two-thirds of all outstanding shares of our voting stock then entitled to vote in the
election of directors; |
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a requirement of approval of
not less than two-thirds of all outstanding shares of our voting stock to amend any bylaws by stockholder action or to amend specific
provisions of our Certificate of Incorporation; and |
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the authority of our board
of directors to issue preferred stock on terms determined by our board of directors without stockholder approval and which preferred
stock may include rights superior to the rights of the holders of our common stock. |
In
addition, because we are incorporated in Delaware, we are governed by the provisions of Section 203 of the DGCL, which may prohibit
certain business combinations with stockholders owning 15% or more of our outstanding voting stock. These anti-takeover provisions
and other provisions in our Certificate of Incorporation and Second Amended and Restated Bylaws (our “Bylaws”) could make
it more difficult for stockholders or potential acquirors to obtain control of our board of directors or initiate actions that are opposed
by our then-current board of directors and could also delay or impede a merger, tender offer, or proxy contest involving us. These provisions
could also discourage proxy contests and make it more difficult for you and other stockholders to elect directors of your choosing or
cause us to take other corporate actions you desire. Any delay or prevention of a change of control transaction or changes in our board
of directors could cause the market price of our common stock to decline.
Our
Certificate of Incorporation provides that the Court of Chancery of the State of Delaware is the exclusive forum for substantially
all disputes between us and our stockholders, which could limit our stockholders’ ability to obtain a favorable judicial forum
for disputes with us or our directors, officers or employees.
Our
Certificate of Incorporation provides that the Court of Chancery of the State of Delaware is the exclusive forum for the following types
of actions or proceedings under Delaware statutory or common law: (i) any derivative action or proceeding brought on our behalf;
(ii) any action or proceeding asserting a claim of breach of a fiduciary duty owed by any of our current or former directors, officers,
or other employees to us or our stockholders; (iii) any action or proceeding asserting a claim against us or any of our current
or former directors, officers, or other employees, arising out of or pursuant to any provision of the DGCL, our Certificate of Incorporation
or Bylaws; (iv) any action or proceeding to interpret, apply, enforce, or determine the validity of our Certificate of Incorporation
or Bylaws; (v) any action or proceeding as to which the DGCL confers jurisdiction to the Court of Chancery of the State of Delaware;
and (vi) any action asserting a claim against us or any of our directors, officers, or other employees governed by the internal
affairs doctrine, in all cases to the fullest extent permitted by law and subject to the court’s having personal jurisdiction over
the indispensable parties named as defendants. These provisions would not apply to suits brought to enforce a duty or liability created
by the Exchange Act. Furthermore, Section 22 of the Securities Act creates concurrent jurisdiction for federal and state courts
over all such Securities Act actions. Accordingly, both state and federal courts have jurisdiction to entertain such claims. To prevent
having to litigate claims in multiple jurisdictions and the threat of inconsistent or contrary rulings by different courts, among other
considerations, our Certificate of Incorporation provides that the federal district courts of the United States of America shall
be exclusive forum for resolving any complaint asserting a cause of action arising under the Securities Act, including all causes of
action asserted against any defendant named in such complaint. While the Delaware courts have determined that such choice of forum provisions
are facially valid, a stockholder may nevertheless seek to bring a claim in a venue other than those designated in the exclusive forum
provisions. In such instance, we would expect to vigorously assert the validity and enforceability of the exclusive forum provisions
of our Certificate of Incorporation. This may require significant additional costs associated with resolving such action in other jurisdictions,
and the provisions may not be enforced by a court in those other jurisdictions.
These
exclusive forum provisions may limit a stockholder’s ability to bring a claim in a judicial forum that it finds favorable for disputes
with us or our directors, officers, or other employees and may discourage these types of lawsuits. In addition, a stockholder that is
unable to bring a claim in the judicial forum of its choosing may be required to incur additional costs in the pursuit of actions that
are subject to these exclusive forum provisions, particularly if the stockholder does not reside in or near Delaware. Furthermore, the
enforceability of similar choice of forum provisions in other companies’ certificates of incorporation or bylaws has been challenged
in legal proceedings, and it is possible that a court could find these types of provisions to be inapplicable or unenforceable. If a
court were to find the exclusive forum provision contained in our Certificate of Incorporation to be inapplicable or unenforceable in
an action, we may incur further significant additional costs associated with resolving such action in other jurisdictions, all of which
could seriously harm our business.
Any
exercise of the outstanding warrants to purchase shares of our common stock would increase the number of shares eligible for future resale
in the public market and result in dilution to our stockholders.
Outstanding
warrants to purchase an aggregate of 4,999,883 shares of our common stock became exercisable in accordance with the terms of the Warrant
Agreement, dated November 19, 2019, between Continental Stock Transfer & Trust Company, as warrant agent, and us (the “Warrant
Agreement”) commencing on October 24, 2021 (the “Public Warrants”). The exercise price of these Public Warrants
is $11.50 per share. To the extent such Public Warrants are exercised, additional shares of our common stock will be issued, which will
result in dilution to the holders of our common stock and increase the number of shares eligible for resale in the public market. Sales
of substantial numbers of such shares in the public market or the fact that such Public Warrants may be exercised could adversely affect
the prevailing market prices of our common stock. However, there is no guarantee that the Public Warrants will ever be in the money prior
to their expiration, and as such, the Public Warrants may expire worthless. See below risk factor, “The Public Warrants may
never be in the money, and they may expire worthless and the terms of the Public Warrants may be amended in a manner adverse to a holder
if holders of at least 50% of the then-outstanding Public Warrants approve of such amendment.”
The
Public Warrants may never be in the money, they may expire worthless and the terms of the Public Warrants may be amended in a manner
adverse to a holder if holders of at least 50% of the then-outstanding Public Warrants approve of such amendment.
The
Public Warrants were issued in registered form under the Warrant Agreement. The Warrant Agreement provides that the terms of the Public
Warrants may be amended without the consent of any holder to cure any ambiguity or correct any defective provision or correct any mistake,
but requires the approval by the holders of at least 50% of the then-outstanding Public Warrants to make any change that adversely affects
the interests of the registered holders of Public Warrants. Accordingly, we may amend the terms of the Public Warrants in a manner adverse
to a holder if holders of at least 50% of the then-outstanding Public Warrants approve of such amendment. Although our ability to amend
the terms of the Public Warrants with the consent of at least 50% of the then-outstanding Public Warrants is unlimited, examples of such
amendments could be amendments to, among other things, increase the exercise price of the Public Warrants, convert the Public Warrants
into cash, shorten the exercise period, or decrease the number of shares of our common stock purchasable upon exercise of a Public Warrant.
We
may redeem your unexpired Public Warrants prior to their exercise at a time that is disadvantageous to you, thereby making your Public
Warrants worthless.
We
have the ability to redeem outstanding Public Warrants at any time after they become exercisable and prior to their expiration, at a
price of $0.01 per Public Warrant, provided that the last reported sales price of our common stock equals or exceeds $18.00 per share
(as adjusted for share subdivisions, share dividends, rights issuances, subdivisions, reorganizations, recapitalizations, and the like)
for any 20 trading days within a 30-trading-day period ending on the third trading day prior to the date we send
the notice of redemption to the warrantholders. If and when the Public Warrants become redeemable by us, we may exercise our redemption
right even if we are unable to register or qualify the underlying securities for sale under all applicable state securities laws. Redemption
of the outstanding Public Warrants could force you to: (i) exercise your Public Warrants and pay the exercise price therefor at
a time when it may be disadvantageous for you to do so; (ii) sell your Public Warrants at the then-current market price when you
might otherwise wish to hold your Public Warrants; or (iii) accept the nominal redemption price that, at the time the outstanding
Public Warrants are called for redemption, is likely to be substantially less than the market value of your Public Warrants.
In
addition, we may redeem your Public Warrants at any time after they become exercisable and prior to their expiration at a price of $0.10
per Public Warrant upon a minimum of 30 days’ prior written notice of redemption; provided that holders will be able to exercise
their Public Warrants prior to redemption for a number of our common stock determined based on the redemption date and the fair market
value of our common stock. The value received upon exercise of the Public Warrants (1) may be less than the value the holders would
have received if they had exercised their Public Warrants at a later time where the underlying share price is higher and (2) may
not compensate the holders for the value of the Public Warrants.