GeoVax Presents Corporate Update at the H.C. Wainwright 25th Annual Global Investment Conference
September 12 2023 - 09:00AM
via NewMediaWire – GeoVax Labs, Inc. (Nasdaq: GOVX), a
biotechnology company developing immunotherapies and vaccines
against cancers and infectious diseases, today announced that its
Chairman and CEO, David Dodd, presented a company overview during
the H.C. Wainwright 25th Annual Global Investment Conference on
September 11. A webcast replay of Mr. Dodd’s presentation can be
viewed here.
During his presentation, Mr. Dodd reviewed the Company’s four
ongoing Phase 2 clinical trials:
GEO-CM04S1 (Next-Generation COVID-19
Vaccine)
- As a primary vaccine in immunocompromised patients (with
hematologic cancers receiving cell transplants or CAR-T therapy).
ClinicalTrials.gov Identifier: NCT04977024.
- As a booster vaccine in immunocompromised patients with chronic
lymphocytic leukemia (CLL), a recognized high-risk group for whom
current mRNA vaccines and monoclonal antibody (MAb) therapies
appear inadequate relative to providing protective immunity.
ClinicalTrials.gov Identifier: NCT05672355.
- As a booster vaccine for healthy patients who have previously
received the Pfizer or Moderna mRNA vaccine. ClinicalTrials.gov
Identifier: NCT04639466.
Gedeptin® (Gene Therapy for Solid
Tumors)
- Evaluating the safety and efficacy of repeat cycles of Gedeptin
therapy in patients with recurrent head and neck cancers whose
tumor(s) are accessible for injection and who have no curable
treatment options. ClinicalTrials.gov
Identifier: NCT03754933.
Commenting on the GEO-CM04S1 clinical program, Mr. Dodd said,
“Our next-generation COVID-19 vaccine is designed to provide
critically needed protection to those individuals with depleted
immune systems, and who are inadequately protected by the currently
authorized vaccines and monoclonal antibody therapies. Using our
MVA platform as its backbone, our vaccine candidate is
‘variant-agnostic’ and we expect it to provide broader, more
durable protection than existing authorized vaccines. We anticipate
multiple significant catalyst events during the remainder of 2023.
We recently completed patient enrollment in the healthy booster
trial, and anticipate completion of enrollment in our CLL trial
soon, while also accelerating enrollment in the cell transplant
trial through multi-site expansion. We also believe our vaccine to
be an excellent example of next-generation vaccines, providing more
robust and durable protection, especially for immunocompromised
individuals who don’t adequately respond to the currently
authorized COVID-19 vaccines or monoclonal antibody therapies.”
Regarding the Gedeptin program, Mr. Dodd stated, “We
expect to soon complete the first stage of this study, which is
being funded in part by the U.S. Food and Drug Administration (FDA)
pursuant to its Orphan Products Clinical Trials Grants Program, and
then initiate an expanded Phase 2 trial focused on expedited FDA
registration. We are excited about the potential for the Gedeptin
‘tumor-agnostic’ platform, which may include expanded development,
both as monotherapy and combination therapy in conjunction with
therapies such as immune checkpoint inhibitors. Possible expansion
indications include breast, prostate, and pancreatic cancers, among
other solid tumors. This program also offers multiple opportunities
for global strategic collaborations and partnerships.”
Mr. Dodd’s concluding comments focused on GeoVax’s advancements
made in its MVA manufacturing process in transforming to a
high-yield, high-capacity continuous cell line system, as well as
the Company’s efforts for achieving expedited registration for the
first U.S.-sourced vaccine against Mpox and smallpox. Mr. Dodd
said, “Our progress in developing a continuous avian cell line
system is nothing short of transformative for manufacturing our
MVA-based vaccines and immunotherapies, and we recently partnered
with Advanced Bioscience Laboratories, Inc. to support the
production of our MVA-based products through late-stage development
and eventual commercialization. Additionally, the recent expansion
of our GEO-CM04S1 rights to include development for Mpox and
smallpox adds to other rights we previously secured from the NIH
covering preclinical, clinical, and commercial uses of the NIH-MVA.
This provides a compelling opportunity to leverage our MVA-based
vaccine expertise and help expand the global public health supply
options available for the worldwide public health threats posed by
SARS-CoV-2, Mpox, and smallpox.”
About GeoVax
GeoVax Labs, Inc. is a clinical-stage biotechnology company
developing novel therapies and vaccines for solid tumor cancers and
many of the world’s most threatening infectious diseases. The
company’s lead program in oncology is a novel oncolytic solid tumor
gene-directed therapy, Gedeptin®, presently in a multicenter Phase
1/2 clinical trial for advanced head and neck cancers. GeoVax’s
lead infectious disease candidate is GEO-CM04S1, a next-generation
COVID-19 vaccine targeting high-risk immunocompromised patient
populations. Currently in three Phase 2 clinical trials, GEO-CM04S1
is being evaluated as a primary vaccine for immunocompromised
patients such as those suffering from hematologic cancers and other
patient populations for whom the current authorized COVID-19
vaccines are insufficient, and as a booster vaccine in patients
with chronic lymphocytic leukemia (CLL). In addition, GEO-CM04S1 is
in a Phase 2 clinical trial evaluating the vaccine as a more
robust, durable COVID-19 booster among healthy patients who
previously received the mRNA vaccines. GeoVax has a leadership team
who have driven significant value creation across multiple life
science companies over the past several decades. For more
information, visit our website: www.geovax.com.
Forward-Looking Statements
This release contains forward-looking statements regarding
GeoVax’s business plans. The words “believe,” “look forward to,”
“may,” “estimate,” “continue,” “anticipate,” “intend,” “should,”
“plan,” “could,” “target,” “potential,” “is likely,” “will,”
“expect” and similar expressions, as they relate to us, are
intended to identify forward-looking statements. We have based
these forward-looking statements largely on our current
expectations and projections about future events and financial
trends that we believe may affect our financial condition, results
of operations, business strategy and financial needs. Actual
results may differ materially from those included in these
statements due to a variety of factors, including whether: GeoVax
is able to obtain acceptable results from ongoing or future
clinical trials of its investigational products, GeoVax’s
immuno-oncology products and preventative vaccines can provoke the
desired responses, and those products or vaccines can be used
effectively, GeoVax’s viral vector technology adequately amplifies
immune responses to cancer antigens, GeoVax can develop and
manufacture its immuno-oncology products and preventative vaccines
with the desired characteristics in a timely manner, GeoVax’s
immuno-oncology products and preventative vaccines will be safe for
human use, GeoVax’s vaccines will effectively prevent targeted
infections in humans, GeoVax’s immuno-oncology products and
preventative vaccines will receive regulatory approvals necessary
to be licensed and marketed, GeoVax raises required capital to
complete development, there is development of competitive products
that may be more effective or easier to use than GeoVax’s products,
GeoVax will be able to enter into favorable manufacturing and
distribution agreements, and other factors, over which GeoVax has
no control.
Further information on our risk factors is contained in our
periodic reports on Form 10-Q and Form 10-K that we have filed and
will file with the SEC. Any forward-looking statement made by us
herein speaks only as of the date on which it is made. Factors or
events that could cause our actual results to differ may emerge
from time to time, and it is not possible for us to predict all of
them. We undertake no obligation to publicly update any
forward-looking statement, whether as a result of new information,
future developments or otherwise, except as may be required by
law.
Contact:GeoVax Labs,
Inc.investor@geovax.com678-384-7220
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