Filed Pursuant to Rule 424(b)(5)
Registration No. 333-231537
PROSPECTUS SUPPLEMENT
(To Prospectus dated June 5, 2019)
1,710,600 SHARES OF COMMON STOCK
Pursuant to this prospectus supplement and the accompanying
prospectus, we are offering 1,710,600 shares of our common stock,
par value $0.001 per share. Our common stock is currently listed on
the Nasdaq Capital Market under the symbol “BPTH.” On February 12,
2021, the last reported sales price per share of our common stock
on the Nasdaq Capital Market was $8.93.
As of the date of this prospectus supplement, the aggregate market
value of our outstanding common stock held by non-affiliates was
$61,243,052.86, based on 5,237,312 shares of outstanding common
stock, of which 5,203,318 shares are held by non-affiliates, and
the last reported sale price of our common stock of $11.77 per
share on February 11, 2021. Pursuant to General Instruction I.B.6
of Form S-3, in no event will we sell securities in a primary
offering with a value exceeding more than one-third of our public
float in any 12-month period so long as our public float remains
below $75,000,000. Following the sale of shares in this offering,
we will have sold securities with an aggregate market value of
$19,956,271.84 pursuant to General Instruction I.B.6 of Form S-3
during the 12-month calendar period that ends on and includes the
date hereof.
The trading price of our common stock has been volatile. From
February 1, 2021 through February 12, 2021, our stock
price has fluctuated from a low of $4.1117 to a high of $24.34. The
high of $24.34 occurred on February 10, 2021, the same day
that the Company publicly announced that the United States Patent
and Trademark Office (“USPTO”) granted the Company a new patent and
that the USPTO had mailed an Issue Notification for a separate
patent scheduled to be issued. As a result of volatility in the
trading price of our common stock, you may not be able to sell your
common stock at or above the public offering price.
Investing in our securities involves a high degree of risk,
including that the trading price of our common stock has been
subject to volatility and investors in this offering may not be
able to sell their shares of common stock at or above the public
offering price. You should review carefully the risks and
uncertainties described in the section titled “Risk Factors” on
page S-6 of this prospectus supplement and under similar
headings in the other documents that are incorporated by reference
into this prospectus supplement.
|
|
Per Share |
|
|
Total |
|
Offering price |
|
$ |
7.60 |
|
|
$ |
13,000,560.00 |
|
Placement agent fees (1) |
|
$ |
0.38 |
|
|
$ |
650,028.00 |
|
Proceeds, before expenses, to us |
|
$ |
7.22 |
|
|
$ |
12,350,532.00 |
|
(1) We have agreed to pay the placement agent a cash fee equal to
5.0% of the gross proceeds received from investors who purchase
securities in the offering. In addition, we have agreed to
reimburse the placement agent for certain expenses as described
under the “Plan of Distribution” on page S-13 of this prospectus
supplement.
We have retained Roth Capital Partners, LLC to act as our exclusive
placement agent in connection with this offering. The placement
agent is not purchasing the securities offered by us in this
offering, and is not required to sell any specific number or dollar
amount of securities, but will assist us in this offering on a
reasonable best efforts basis. There is no required minimum number
of shares of common stock that must be sold as a condition to
completion of this offering. Because there is no minimum offering
amount required as a condition to the closing of this offering, the
actual offering amount, placement agent fees and proceeds to us are
not presently determinable and may be substantially less than the
maximum amounts set forth above. We may sell fewer than all of the
shares of common stock offered hereby, which may significantly
reduce the amount of proceeds received by us, and investors in this
offering will not receive a refund in the event that we do not sell
an amount of common stock sufficient to pursue the business goals
outlined in this prospectus supplement and the accompanying
prospectus.
Neither the Securities and Exchange Commission nor any state
securities commission has approved or disapproved of these
securities or passed on the adequacy or accuracy of this prospectus
supplement or the accompanying prospectus. Any representation to
the contrary is a criminal offense.
Delivery of the shares of common stock offered hereby is expected
to take place on or about February 18, 2021, subject to
satisfaction of certain conditions.
Roth Capital
Partners
Prospectus supplement dated February 16, 2021
TABLE OF CONTENTS
Prospectus Supplement
Prospectus
ABOUT
THIS PROSPECTUS SUPPLEMENT
This prospectus supplement and the accompanying prospectus are part
of a registration statement that we filed with the U.S. Securities
and Exchange Commission utilizing a “shelf” registration process.
This document is in two parts. The first part is this prospectus
supplement, which describes the terms of this offering and also
adds to and updates information contained in the accompanying
prospectus as well as the documents incorporated by reference into
this prospectus supplement and the accompanying prospectus. The
second part, the accompanying prospectus, gives more general
information about securities we may offer from time to time, some
of which does not apply to this offering. This prospectus
supplement and the accompanying prospectus incorporate by reference
important business and financial information about us that is not
included in or delivered with this prospectus supplement and the
accompanying prospectus.
You should rely only on the information we have provided or
incorporated by reference in this prospectus supplement or in the
accompanying prospectus. If information in this prospectus
supplement is inconsistent with the accompanying prospectus or any
document incorporated by reference therein filed prior to the date
of this prospectus supplement, you should rely on this prospectus
supplement; provided that if any statement in one of these
documents is inconsistent with a statement in another document
having a later date—for example, a document incorporated by
reference in the accompanying prospectus—the statement in the
document having the later date modifies or supersedes the earlier
statement. We have not authorized anyone to provide you with
different information. No dealer, salesperson or other person is
authorized to give any information or to represent anything not
contained in this prospectus or the applicable prospectus
supplement. You must not rely on any unauthorized information or
representation. You should assume that the information in this
prospectus supplement and accompanying prospectus is accurate only
as of the dates on the front of the respective document and that
any information we have incorporated by reference is accurate only
as of the date of the document incorporated by reference. Our
business, financial condition, results of operations and prospects
may have changed since those dates. You should read this prospectus
supplement, the accompanying prospectus and the documents
incorporated by reference in this prospectus supplement and the
accompanying prospectus when making your investment decision.
Unless the context requires otherwise, references in this
prospectus supplement or the accompanying prospectus to “we,”
“our,” “us,” “the Company” and “Bio-Path” refer to Bio-Path
Holdings, Inc. and its wholly-owned subsidiary. Bio-Path
Holdings, Inc.’s wholly-owned subsidiary, Bio-Path, Inc.,
is sometimes referred to herein as “Bio-Path Subsidiary.”
PROSPECTUS
SUPPLEMENT SUMMARY
This summary highlights selected information contained elsewhere
in this prospectus supplement, in the accompanying prospectus or in
documents incorporated by reference. This summary does not contain
all of the information that you should consider before making an
investment decision. This prospectus supplement and the
accompanying prospectus include or incorporate by reference
information about this offering, our business and our financial and
operating data. You should carefully read the entire prospectus
supplement, the accompanying prospectus, including under the
sections titled “Risk Factors” included therein, and the documents
incorporated by reference into this prospectus supplement and the
accompanying prospectus, before making an investment
decision.
Our Company
We are a clinical and preclinical stage oncology focused RNAi
nanoparticle drug development company utilizing a novel technology
that achieves systemic delivery for target specific protein
inhibition for any gene product that is over-expressed in disease.
Our drug delivery and antisense technology, called DNAbilize®, is a
platform that uses P-ethoxy, which is a deoxyribonucleic acid (DNA)
backbone modification that is intended to protect the DNA from
destruction by the body’s enzymes when circulating in vivo,
incorporated inside of a lipid bilayer having neutral charge. We
believe this combination allows for high efficiency loading of
antisense DNA into non-toxic, cell-membrane-like structures for
delivery of the antisense drug substance into cells. In vivo, the
DNAbilize® delivered antisense drug substances are systemically
distributed throughout the body to allow for reduction or
elimination of target proteins in blood diseases and solid tumors.
Through testing in numerous animal studies and treatment in over 80
patients, the Company’s DNAbilize® drug candidates have
demonstrated an excellent safety profile. DNAbilize® is a
registered trademark of the Company.
Using
DNAbilize® as a platform for drug development and manufacturing, we
currently have four drug candidates in development to treat at
least five different cancer disease indications. Our lead drug
candidate, prexigebersen (pronounced prex” i je ber’ sen), which
targets growth factor receptor-bound protein 2 (Grb2), initially
started the efficacy portion of a Phase 2 clinical trial for
untreated acute myeloid leukemia (“AML”) patients in combination
with low-dose cytarabine (“LDAC”). The interim data we released on
March 6, 2019 showed that 11 (65%) of the 17 evaluable
patients had a response, including five (29%) who achieved CR,
including one CRi and one morphologic leukemia
free state, and six (35%) stable disease responses, including two
patients who had greater than a 50% reduction in bone marrow
blasts. However, DNA hypomethylating agents are now the most
frequently used agents in the treatment of elderly AML patients in
the U.S. and Europe. Accordingly, a second cohort of untreated AML
patients was subsequently added to the clinical trial for treatment
with prexigebersen in combination with decitabine, a DNA
hypomethylating agent. As a result, Stage 2 of the Phase 2 trial in
AML dropped was amended to, among other things, remove the
combination treatment of prexigebersen and LDAC and replace it with
the combination treatment of prexigebersen and decitabine. Since
decitabine is also used as a treatment for relapsed/refractory AML
patients, a second cohort of relapsed/refractory AML patients was
also added to the study.
The U.S. Food and Drug Administration (“FDA”) recently granted
approval of venetoclax in combination with LDAC, decitabine, or
azacytidine (the latter two drugs are DNA hypomethylating agents)
as frontline therapy for newly diagnosed AML in adults 75 years or
older, or who have comorbidities precluding intensive induction
chemotherapy. We believe this recent frontline therapy approval
provides an opportunity to include prexigebersen with the
combination therapy for the treatment of de novo AML
patients. Preclinical efficacy studies for the triple combination
treatment of prexigebersen, decitabine and venetoclax in AML have
been successfully completed. In the preclinical efficacy studies,
four AML cancer cell lines were treated with three different
combinations of decitabine, venetoclax and prexigebersen. Decrease
in AML cell viability was the primary measure of efficacy. The
triple combination of decitabine, venetoclax and prexigebersen
showed significant improvement in efficacy in three of the four AML
cell lines. Based on these results, the Company believes that
adding prexigebersen to the treatment combination of decitabine and
venetoclax could lead to improved efficacy in AML patients. The
amendment for Stage 2 of this Phase 2 clinical trial to add the
triple combination treatment comprised of prexigebersen, decitabine
and venetoclax had been approved by the FDA.
Bio-Path’s approved amended Stage 2 for this Phase 2 clinical trial
has three cohorts of patients. The first two cohorts will treat
patients with the triple combination of prexigebersen, decitabine
and venetoclax. The first cohort will include untreated AML
patients, and the second cohort will include relapsed/refractory
AML patients. Finally, the third cohort will treat
relapsed/refractory AML patients, who are venetoclax-resistant or
-intolerant, with the two-drug combination of prexigebersen and
decitabine. The full trial design plans have approximately 98
evaluable patients for the first cohort having untreated AML
patients with a preliminary review performed after 19 evaluable
patients and a formal interim analysis after 38 evaluable patients.
The full trial design plans have approximately 54 evaluable
patients for each of the second cohort, having relapsed/refractory
AML patients, and the third cohort, having AML patients who are
venetoclax-resistant or -intolerant, in each case with a review
performed after 19 evaluable patients. The study is anticipated to
be conducted at ten clinical sites in the U.S., and Gail J. Roboz,
MD will be the national coordinating Principal Investigator for the
Phase 2 trial. Dr. Roboz is a professor of medicine and
director of the Clinical and Translational Leukemia Program at the
Weill Medical College of Cornell University and the New
York-Presbyterian Hospital in New York City. On August 13,
2020, we announced the enrollment and dosing of the first patient
in this approved amended Stage 2 of the Phase 2 clinical study.
Our second drug candidate, Liposomal Bcl-2 (“BP1002”), targets the
protein Bcl-2, which is responsible for driving cell survival in up
to 60% of all cancers. On November 21, 2019, we announced that
the FDA cleared an IND application for BP1002. An initial Phase 1
clinical trial will evaluate the safety of BP1002 in
refractory/relapsed lymphoma and chronic lymphocytic leukemia
(“CLL”) patients. Initially, a total of six evaluable patients are
scheduled to be treated with BP1002 monotherapy in a standard 3+3
design. The Phase 1 clinical trial is being conducted at several
leading cancer centers, including The University of Texas MD
Anderson Cancer Center (“MD Anderson”), the Georgia Cancer Center
and the Sarah Cannon Research Institute, and is now open for
enrollment. Ian W. Flynn, MD is the national coordinating Principal
Investigator for the Phase 1 trial. Dr. Flynn serves as the
director of lymphoma research at the Sarah Cannon Research
Institute.
Our third drug candidate, Liposomal STAT3 (“BP1003”), targets the
STAT3 protein and is currently in IND enabling studies as a
potential treatment of pancreatic cancer, non-small cell lung
cancer (“NSCLC”) and AML. Preclinical models have shown BP1003 to
inhibit cell viability and STAT3 protein expression in NSCLC and
AML cell lines. Further, BP1003 successfully penetrated pancreatic
tumors and significantly enhanced the efficacy of gemcitabine, a
treatment for patients with advanced pancreatic cancer, in a
pancreatic cancer patient derived tumor model. Our lead indication
for BP1003 is pancreatic cancer due to the severity of this disease
and the lack of effective, life-extending treatments. For example,
pancreatic adenocarcinoma is projected to be the second most lethal
cancer behind lung cancer by 2030. Typical survival for a
metastatic pancreatic cancer patient is about three to six months
from diagnosis. We expect to complete several IND enabling studies
of BP1003 in 2021. If those studies are successful, our goal is to
file an IND in late 2021 for the first-in-humans Phase 1 study of
BP1003 in patients with refractory, metastatic solid tumors,
including pancreatic cancer and NSCLC.
In addition, a modified product named prexigebersen-A, Bio-Path’s
fourth drug candidate, has shown to enhance chemotherapy efficacy
in preclinical solid tumor models. Prexigebersen-A incorporates the
same drug substance as prexigebersen but has a slightly modified
formulation designed to enhance nanoparticle properties. In late
2019, we filed an Investigational New Drug (“IND”) application to
initiate a Phase 1 clinical trial of prexigebersen-A in patients
with solid tumors, including ovarian, endometrial, pancreatic and
breast cancer. Ovarian cancer is one of the most common type of
gynecologic malignancies, with approximately 50% of all cases
occurring in women older than 63 years. This trial is expected to
commence after the IND has been cleared by the FDA, which we
currently anticipate being in 2021.
Our DNAbilize® technology-based products are available for
out-licensing or partnering. We intend to apply our drug delivery
technology template to new disease-causing protein targets to
develop new nanoparticle antisense RNAi drug candidates. We have a
new product identification template in place to define a process of
scientific, preclinical, commercial and intellectual property
evaluation of potential new drug candidates for inclusion into our
drug product development pipeline. As we expand, we will look at
indications where a systemic delivery is needed and antisense RNAi
nanoparticles can be used to slow, reverse or cure a disease,
either alone or in combination with another drug. On
September 25, 2019, we announced that the United States Patent
and Trademark Office (“USPTO”) issued a patent for claims related
to DNAbilize®, including its use in the treatment of cancers,
autoimmune diseases and infectious diseases. This is the second
patent issued to the Company for its platform technology. In
February 2021, the Company announced that the USPTO has
granted U.S. Patent No. 10,898,506 titled, "P-ethoxy nucleic
acids for liposomal formulation." The new patent builds on earlier
patents granted that protect the platform technology for
DNAbilize®, the Company’s novel RNAi nanoparticle drugs.
The new patent is the third patent in our family of platform
intellectual property and offers expanded defense of our
DNAbilize® platform technology. In addition, the USPTO
has mailed an Issue Notification for a patent related to the
Company’s lead product candidate, prexigebersen, in combination
with either a cytidine analogue, such as decitabine, or the Bcr-Abl
tyrosine kinase inhibitors dasatinib and nilotinib. The new patent
is scheduled to issue as U.S. Patent No. 10,927,379 on
February 23, 2021. This patent will offer target-specific
protection for on-going clinical trials using prexigebersen in
combination with decitabine as a treatment for AML. We continue our
efforts to build protection around our technology as it safeguards
our platform technology and target-specific technology, is a
deterrent to would-be competitors and creates value around our core
competencies.
We have certain intellectual property as the basis for our current
drug products in clinical development, prexigebersen,
prexigebersen-A, BP1002 and BP1003. We are developing RNAi
antisense nanoparticle drug candidates based on our own patented
technology to treat cancer and autoimmune disorders where targeting
a single protein may be advantageous and result in reduced patient
adverse effects as compared to small molecule inhibitors with
off-target and non-specific effects. We have composition of matter
and method of use intellectual property for the design and
manufacture of antisense RNAi nanoparticle drug products.
Recent Developments
On February 10, 2021, we announced that the USPTO granted U.S.
Patent No. 10,898,506 titled, “P-ethoxy nucleic acids for
liposomal formulation.” We also announced that the USPTO mailed an
Issue Notification for a patent related to the Company’s lead
product candidate, prexigebersen, in combination with either a
cytidine analogue, such as decitabine, or the Bcr-Abl tyrosine
kinase inhibitors dasatinib and nilotinib.
Subsequent to September 30, 2020, we sold 1,128,800 shares of
our common stock under the Company’s At-The-Market Offering
Agreement (the “Offering Agreement”) with H. C.
Wainwright & Co., LLC and issued 416,655 shares of our
common stock pursuant to the exercise warrants to purchase shares
of our common stock.
Corporate Information
The Company was incorporated in May 2000 as a Utah
corporation. In February 2008, Bio-Path Subsidiary completed a
reverse merger with the Company, which at the time was traded over
the counter and had no current operations. The prior name of the
Company was changed to Bio-Path Holdings, Inc. and the
directors and officers of Bio-Path Subsidiary became the directors
and officers of Bio-Path Holdings, Inc. On March 10,
2014, our common stock ceased trading on the OTCQX and commenced
trading on the Nasdaq Capital Market under the ticker symbol
“BPTH.” Effective December 31, 2014, we changed our state of
incorporation from Utah to Delaware through a statutory conversion
pursuant to the Utah Revised Business Corporation Act and the
Delaware General Corporation Law.
On February 8, 2018, we effected a reverse stock split of our
outstanding shares of common stock at a ratio of 1-for-10, and our
common stock began trading on the split-adjusted basis on the
Nasdaq Capital Market at the commencement of trading on
February 9, 2018. In addition, on January 17, 2019, we
effected a reverse stock split of our outstanding shares of common
stock at a ratio of 1-for-20, and our common stock began trading on
the split-adjusted basis on the Nasdaq Capital Market at the
commencement of trading on January 18, 2019. All common stock
share and per share amounts in this prospectus supplement and in
the accompanying prospectus have been adjusted to give effect to
both the 1-for-10 reverse stock split and the 1-for-20 reverse
stock split, retrospectively.
Our principal executive offices are located at 4710 Bellaire
Boulevard, Suite 210, Bellaire, Texas 77401, and our telephone
number is (832) 742-1357. Our Internet address is
www.biopathholdings.com. None of the information on our
website forms a part of, or incorporated by reference into, this
prospectus supplement or the accompanying prospectus.
The Offering
Common
stock offered by us |
|
1,710,600 shares.
|
|
|
|
Common
stock to be outstanding immediately after this offering
(1) |
|
6,947,912 shares (assuming that we sell the maximum number of
shares of common stock offered in this offering).
|
|
|
|
Offering
price per share |
|
$7.60 per share.
|
|
|
|
Use
of proceeds |
|
We
currently expect to use the net proceeds from this offering for
working capital and general corporate purposes. See “Use of
Proceeds” on page S-11 |
|
|
|
Risk
factors |
|
An
investment in our company involves a high degree of risk, including
that the trading price of our common stock has been subject to
volatility and investors in this offering may not be able to sell
their shares of common stock at or above the public offering price.
Please refer to the sections titled “Risk Factors,” “Special Note
Regarding Forward-Looking Statements” and other information
included or incorporated by reference in this prospectus supplement
and the accompanying prospectus for a discussion of factors you
should carefully consider before investing our
securities. |
|
|
|
Nasdaq
Capital Market Symbol |
|
“BPTH” |
(1) The number of shares of common stock to be outstanding
after this offering is based on 5,237,312 shares of our common
stock outstanding as of the date of this prospectus supplement,
which excludes as of such date:
|
· |
274,008
shares of common stock reserved for issuance upon the exercise of
outstanding options granted under our equity incentive plans with a
weighted average exercise price of $20.57 per share; |
|
|
|
|
· |
402,724
additional shares of common stock reserved for future issuance
under our 2017 Stock Incentive Plan; and |
|
|
|
|
· |
442,043
shares of common stock issuable upon exercise of outstanding
warrants with a weighted average exercise price of $26.94 per
share. |
RISK FACTORS
An investment in our company involves a high degree of risk.
Before you make a decision to invest in our securities, you should
consider carefully the risks described below, as well as the risks
described in or incorporated by reference in this prospectus
supplement and the accompanying prospectus, including the risks and
uncertainties discussed under the section titled “Risk Factors” in
our most recent Annual Report on Form 10-K and any subsequent
Quarterly Reports on Form 10-Q or Current Reports on
Form 8-K, and all other documents incorporated by reference
into this prospectus supplement and accompanying prospectus, as
updated by our subsequent filings under the Securities Exchange Act
of 1934, as amended (the “Exchange Act”).
Any of these risks could have a material adverse effect on our
business, prospects, financial condition and results of operations.
In any such case, the trading price of our securities could decline
and you could lose all or part of your investment. Additional risks
not presently known to us or that we currently deem immaterial may
also adversely affect our business operations.
This is a best efforts offering, no minimum amount of shares
is required to be sold, and we may not raise the amount of capital
we believe is required for our business.
We have retained Roth Capital Partners, LLC to act as our exclusive
placement agent in connection with this offering. The placement
agent has agreed to use its reasonable best efforts to solicit
offers to purchase the shares of common stock in this offering. The
placement agent has no obligation to buy any of the shares of
common stock from us or to arrange for the purchase or sale of any
specific number or dollar amount of the shares of common stock.
There is no required minimum number of securities that must be sold
as a condition to completion of this offering. Because there is no
minimum offering amount required as a condition to the closing of
this offering, the actual offering amount, placement agent fees and
proceeds to us are not presently determinable and may be
substantially less than the maximum amounts set forth herein. We
may sell fewer than all of the shares of common stock offered
hereby, which may significantly reduce the amount of proceeds
received by us, and investors in this offering will not receive a
refund in the event that we do not sell an amount of shares
sufficient to pursue the business goals outlined in this
prospectus. Thus, we may not raise the amount of capital we believe
is required for our business and may need to raise additional
funds, which may not be available or available on terms acceptable
to us. Despite this, any proceeds from the sale of shares offered
by us will be available for our immediate use, and because there is
no escrow account and no minimum offering amount in this offering,
investors could be in a position where they have invested in us,
but we are unable to fulfill our objectives.
You will experience immediate and substantial dilution in the
net tangible book value per share of the common stock you
purchase.
Since the price per share of our common stock being offered is
substantially higher than the net tangible book value per share of
our common stock, you will suffer substantial dilution in the net
tangible book value of the common stock you purchase in this
offering. Based on an offering price of $7.60 per share of common
stock, if you purchase shares of common stock in this offering, you
will suffer immediate and substantial dilution of approximately
$2.41 per share in the net tangible book value of the common stock.
See the section titled “Dilution” in this prospectus supplement for
a more detailed discussion of the dilution you will incur if you
purchase common stock in this offering.
There may be future sales of our securities or other dilution
of our equity, which may adversely affect the market price of our
common stock.
With limited exceptions, we are generally not restricted from
issuing additional common stock, including any securities that are
convertible into or exchangeable for, or that represent the right
to receive, common stock. The market price of our common stock
could decline as a result of sales of common stock or securities
that are convertible into or exchangeable for, or that represent
the right to receive, common stock after this offering or the
perception that such sales could occur.
Our management has significant flexibility in using the net
proceeds of this offering.
We currently intend generally to use the net proceeds from this
offering for working capital and general corporate purposes. Our
management will have significant flexibility in applying the net
proceeds of this offering. Management’s failure to use these funds
effectively would have an adverse effect on the value of our common
stock and could make it more difficult and costly to raise funds in
the future.
We are a clinical stage biotechnology company with no
significant revenue. We have incurred significant operating losses
since our inception, and we expect to incur losses for the
foreseeable future and may never achieve profitability.
We have incurred significant operating losses since our inception.
As of September 30, 2020, we had an accumulated deficit of
$64.7 million. To date, we have not generated any revenue from the
sale of our drug candidates and we do not expect to generate any
revenue from sales of our drug candidates for the foreseeable
future. We expect to continue to incur significant operating losses
and we anticipate that our losses may increase substantially as we
expand our drug development programs and commercialization
efforts.
To achieve profitability, we must successfully develop and obtain
regulatory approval for one or more of our drug candidates and
effectively commercialize any drug candidates we develop. Even if
we succeed in developing and commercializing one or more of our
drug candidates, we may not be able to generate sufficient revenue
and we may never be able to achieve or sustain profitability.
We will continue to require substantial additional capital
for the foreseeable future. If we are unable to raise additional
capital when needed, we may be forced to delay, reduce or eliminate
our drug development programs and commercialization
efforts.
We expect to continue to incur significant operating expenses in
connection with our ongoing activities, including conducting
clinical trials, manufacturing and seeking regulatory approval of
our drug candidates, prexigebersen, BP1002, BP1003 and
prexigebersen-A. In addition, if we obtain regulatory approval of
one or more of our drug candidates, we expect to incur significant
commercialization expenses related to product sales, marketing,
manufacturing and distribution.
As of September 30, 2020, we had $12.1 million in cash on
hand, compared to $20.4 million as of December 31, 2019. Our
ongoing future capital requirements will depend on numerous
factors, including:
|
· |
the rate of progress, results and costs of completion of
ongoing clinical trials of our drug candidates; |
|
· |
the rate of progress, results and costs of completion of the
ongoing preclinical testing of prexigebersen, BP1002, BP1003 and
prexigebersen-A; |
|
· |
the size, scope, rate of progress, results and costs of
completion of any potential future clinical trials and preclinical
tests of our drug candidates that we may initiate; |
|
· |
the costs to obtain adequate supply of the compounds necessary
for our drug candidates; |
|
· |
the costs of obtaining regulatory approval of our drug
candidates; |
|
· |
the scope, prioritization and number of drug development
programs we pursue; |
|
· |
the costs for preparing, filing, prosecuting, maintaining and
enforcing our intellectual property rights and defending
intellectual property-related claims; |
|
· |
the extent to which we acquire or in-license other products and
technologies and the costs to develop those products and
technologies; |
|
· |
the costs of future commercializing activities, including
product sales, marketing, manufacturing and distribution, of any of
our drug candidates or other products for which marketing approval
has been obtained; |
|
· |
our ability to establish strategic collaborations and licensing
or other arrangements on terms favorable to us; and |
|
· |
competing technological and market developments. |
Any additional fundraising efforts may divert our management from
their day to day activities, which may adversely affect our ability
to develop and commercialize our drug candidates. Our ability to
raise additional funds will depend, in part, on the success of our
product development activities and other factors related to
financial, economic and market conditions, many of which are beyond
our control. There can be no assurance that we will be able to
raise additional capital when needed or on terms that are favorable
to us, if at all. If adequate funds are not available on a timely
basis, we may be forced to:
|
· |
delay, reduce the scope of or eliminate one or more of our drug
development programs; |
|
· |
relinquish, license or otherwise dispose of rights to
technologies, drug candidates or products that we would otherwise
seek to develop or commercialize ourselves at an earlier stage or
on terms that are less favorable than might otherwise be available;
or |
|
· |
liquidate and dissolve the Company. |
If our operating plans change, we may require additional capital
sooner than planned. Such additional financing may not be available
when needed or on terms favorable to us. In addition, we may seek
additional capital due to favorable market conditions or strategic
considerations, even if we believe we have sufficient funds for our
current and future operating plan.
The trading price of our common stock has been volatile and
is likely to be volatile in the future.
The trading price of our common stock has been highly volatile.
From January 1, 2018 through December 31, 2020, our stock
price has fluctuated from a low of $1.61 to a high of $73.52, after
adjustment for reverse stock splits. In addition, from
February 1, 2021 through February 12, 2021, our stock
price has fluctuated from a low of $4.1117 to a high of $24.34. The
high of $24.34 occurred on February 10, 2021, the same day
that the Company publicly announced that the USPTO granted the
Company a new patent and that the USPTO had mailed an Issue
Notification for a separate patent scheduled to be issued. The
market price for our common stock will be affected by a number of
factors, including:
|
· |
the denial or delay of regulatory approvals of our drug
candidates or receipt of regulatory approval of competing
products; |
|
· |
our ability to accomplish clinical, regulatory and other drug
development milestones; |
|
· |
the ability of our drug candidates, if they receive regulatory
approval, to achieve market success; |
|
· |
the performance of third-party manufacturers and
suppliers; |
|
· |
developments with respect to patents and other intellectual
property rights; |
|
· |
sales of common stock or other securities by us or our
stockholders in the future; |
|
· |
additions or departures of key scientific or management
personnel; |
|
· |
disputes or other developments relating to proprietary rights,
including patents, litigation matters and our ability to obtain
patent protection for our drug candidates; |
|
· |
trading volume of our common stock; |
|
· |
investor perceptions about us and our industry; |
|
· |
public reaction to our press releases, other public
announcements and SEC and other filings; |
|
· |
the failure of analysts to cover us, or changes in analysts’
estimates or recommendations; |
|
· |
the failure by us to meet analysts’ projections or
guidance; |
|
· |
general market conditions and other factors unrelated to our
operating performance or the operating performance of our
competitors; and |
|
· |
other risk factors described elsewhere in our public
filings. |
Continued market fluctuations could result in extreme volatility in
the price of our common stock, which could cause a decline in the
value of our common stock and the loss of some or all of your
investment. The stock prices of many companies in the biotechnology
industry have experienced wide fluctuations that have often been
unrelated to the operating performance of these companies.
Following periods of volatility in the market price of a company’s
securities, securities class action litigation often has been
initiated against a company. If any class action litigation is
initiated against us, we may incur substantial costs and our
management’s attention may be diverted from our operations, which
could materially adversely affect our business and financial
condition.
SPECIAL NOTE REGARDING
FORWARD-LOOKING STATEMENTS
This prospectus supplement, the accompanying prospectus and the
documents incorporated by reference into this prospectus supplement
and the accompanying prospectus contain “forward-looking
statements” within the meaning of Section 27A of the
Securities Act and Section 21E of the Exchange Act.
Forward-looking statements can be identified by words such as
“anticipate,” “expect,” “intend,” “plan,” “believe,” “seek,”
“estimate,” “project,” “goal,” “strategy,” “future,” “likely,”
“may,” “should,” “will” and variations of these words and similar
references to future periods, although not all forward-looking
statements contain these identifying words. Forward-looking
statements are neither historical facts nor assurances of future
performance. Instead, they are based on our current beliefs,
expectations and assumptions regarding the future of our business,
future plans and strategies, projections, anticipated events and
trends, the economy and other future conditions. Because
forward-looking statements relate to the future, they are subject
to inherent risks, uncertainties, and changes in circumstances,
including but not limited to risk factors incorporated by reference
under “Item 1A. Risk Factors” to Part I of our Annual Report on Form 10-K for
the fiscal year ended December 31, 2019 and other factors
described elsewhere in this prospectus supplement, the accompanying
prospectus or in our current and future filings with the SEC. As a
result, our actual results may differ materially from those
expressed or forecasted in the forward-looking statements, and you
should not rely on such forward-looking statements. You should
carefully read this prospectus supplement and the accompanying
prospectus, together with the information incorporated by reference
herein and therein as described under the sections titled “Where
You Can Find More Information,” completely and with the
understanding that our actual future results may be materially
different from what we expect. We can give no assurances that any
of the events anticipated by the forward-looking statements will
occur or, if any of them do, what impact they will have on our
results of operations and financial condition. Important factors
that could cause our actual results and financial condition to
differ materially from those indicated in the forward-looking
statements include, among others, the following:
|
· |
the
impact, risks and uncertainties related to COVID-19 and actions
taken by governmental authorities or others in connection
therewith; |
|
· |
our
lack of significant revenue to date, our history of recurring
operating losses and our expectation of future operating
losses; |
|
· |
our
need for substantial additional capital and our need to delay,
reduce or eliminate our drug development and commercialization
efforts if we are unable to raise additional capital; |
|
· |
the
highly-competitive nature of the pharmaceutical and biotechnology
industry and our ability to compete effectively; |
|
· |
the
success of our plans to use collaboration arrangements to leverage
our capabilities; |
|
· |
our
ability to retain and attract key personnel; |
|
· |
the
risk of misconduct of our employees, agents, consultants and
commercial partners; |
|
· |
disruptions
to our operations due to expansions of our operations; |
|
· |
the
costs we would incur if we acquire or license technologies,
resources or drug candidates; |
|
· |
risks
associated with product liability claims; |
|
· |
our
reliance on information technology systems and the liability or
interruption associated with cyber-attacks or other breaches of our
systems; |
|
· |
our
ability to use net operating loss carryforwards; |
|
· |
provisions
in our charter documents and state law that may prevent a change in
control; |
|
· |
work
slowdown or stoppage at government agencies could negatively
impact our business; |
|
· |
our
need to complete extensive clinical trials and the risk that we may
not be able to demonstrate the safety and efficacy of our drug
candidates; |
|
· |
risks
that that our clinical trials may be delayed or
terminated; |
|
· |
our
ability to obtain domestic and foreign regulatory approval for our
drug candidates; |
|
· |
changes
in existing laws and regulations affecting the healthcare
industry; |
|
· |
our
reliance on third parties to conduct clinical trials for our drug
candidates; |
|
· |
our
ability to maintain orphan drug exclusivity for our drug
candidates; |
|
· |
our
reliance on third parties for manufacturing our clinical drug
supplies; |
|
· |
risks
associated with the manufacture of our drug candidates; |
|
· |
our
ability to establish sales and marketing capabilities relating to
our drug candidates; |
|
· |
market
acceptance of our drug candidates; |
|
· |
third-party
payor reimbursement practices; |
|
· |
our
ability to adequately protect the intellectual property of our drug
candidates; |
|
· |
infringement
on the intellectual property rights of third parties; |
|
· |
costs
and time relating to litigation regarding intellectual property
rights; |
|
· |
our
ability to adequately prevent disclosure by our employees or others
of trade secrets and other proprietary information; |
|
· |
our
need to raise additional capital; |
|
· |
the
volatility of the trading price of our common stock; |
|
· |
our
common stock being thinly traded; |
|
· |
our
ability to issue shares of common or preferred stock without
approval from our stockholders; |
|
· |
our
ability to pay cash dividends; |
|
· |
costs
and expenses associated with being a public company;
and |
|
· |
our
ability to maintain compliance with the listing standards of the
Nasdaq Capital Market. |
Any forward-looking statement made by us in this prospectus
supplement, the accompanying prospectus and the documents
incorporated by reference herein and therein is based only on
information currently available to us and speaks only as of the
date on which it is made. We undertake no obligation to publicly
update any forward-looking statement, whether as a result of new
information, future developments or otherwise. However, you should
carefully review the risk factors set forth in other reports or
documents we file from time to time with the SEC.
USE OF PROCEEDS
We expect to receive net proceeds from this offering of
approximately $12.2 million after deducting the placement agent
fees and estimated offering expenses payable by us. We currently
intend to use the net proceeds from this offering for working
capital and general corporate purposes.
However, the amount and timing of what we actually spend for these
purposes may vary and will depend on a number of factors, including
our future revenue and cash generated by operations, if any, and
the other factors described in “Risk Factors.” Accordingly, our
management will have discretion and flexibility in applying the net
proceeds of this offering.
Because there is no minimum offering amount required as a condition
to the closing of this offering, the actual offering amount,
placement agent fees and proceeds to us are not presently
determinable and may be substantially less than the amount set
forth herein. We may sell fewer than all of the shares of common
stock offered hereby, which may significantly reduce the amount of
proceeds received by us. Thus, we may not raise the amount of
capital we believe is required for our business and may need to
raise additional funds, which may not be available or available on
terms acceptable to us.
DILUTION
If you invest in our securities, you will experience immediate and
substantial dilution to the extent of the difference between the
amount per share paid in this offering and the adjusted net
tangible book value per share of our common stock immediately after
the offering.
Our net tangible book value per share is determined by subtracting
our total liabilities from our total tangible assets, which is
total assets less intangible assets, and dividing this amount by
the number of shares of common stock outstanding. The historical
net tangible book value of our common stock as of September 30,
2020 was approximately $13.2 million, or $3.57 per share, based on
3,691,857 shares of common stock outstanding at September 30, 2020.
Subsequent to September 30, 2020, we sold 1,128,800 shares of our
common stock under the Offering Agreement with H. C. Wainwright
& Co., LLC for net proceeds of approximately $6.5 million and
issued 416,655 pursuant to the exercise warrants to purchase shares
of our common stock for net proceeds of approximately $4.1 million.
After giving effect to the sales under the Offering Agreement and
the exercise of warrants to purchase shares of our common stock,
the pro forma net tangible book value of our common stock as of
September 30, 2020 would have been approximately $23.8 million, or
$4.55 per share, based on 5,237,312 shares of common stock
outstanding.
After giving effect to the sales under the Offering Agreement and
the exercise of warrants to purchase shares of our common stock
described above, as well as our sale of shares of common stock to
be sold in this offering, and after deducting the placement agent
fees and our estimated offering expenses payable by us, our pro
forma as adjusted net tangible book value as of September 30, 2020
would have been approximately $36.0 million, or $5.19 per share of
common stock. This represents an immediate increase in net tangible
book value of $0.64 per share to existing stockholders and an
immediate dilution of $2.41 per share to new investors in this
offering. The following table illustrates this dilution on a per
share basis:
Offering price per share |
|
|
|
|
|
$ |
7.60 |
|
Pro forma net tangible book value per share as of
September 30, 2020, after giving effect to the sales under the
Offering Agreement and the exercise of warrants to purchase shares
of our common stock described above |
|
$ |
4.55 |
|
|
|
|
|
Increase in net tangible book value per share
attributable to new investors |
|
$ |
0.64 |
|
|
|
|
|
As adjusted net tangible book value per share
after the offering |
|
|
|
|
|
$ |
5.19 |
|
Dilution per share to new investors |
|
|
|
|
|
$ |
2.41 |
|
The above discussion and table are based on 5,237,312 shares of our
common stock outstanding as of September 30, 2020, after
giving effect to the sales under the Offering Agreement and the
exercise of warrants to purchase shares of our common stock
described above, which excludes as of September 30, 2020:
|
· |
274,008 shares of common stock reserved for
issuance upon the exercise of outstanding options granted under our
equity incentive plans with a weighted average exercise price of
$20.57 per share; |
|
|
|
|
· |
402,724 additional shares of common stock
reserved for future issuance under our 2017 Stock Incentive
Plan; |
|
|
|
|
· |
442,043 shares of common stock issuable upon
exercise of outstanding warrants with a weighted average exercise
price of $26.94 per share. |
The above illustration of dilution per share to investors
participating in this offering assumes no exercise of outstanding
options to purchase our common stock or outstanding warrants to
purchase shares of our common stock. To the extent that any of
these outstanding options or warrants are exercised or we issue
additional shares under our equity incentive plans, there will be
further dilution to new investors. In addition, we may choose to
raise additional capital due to market conditions or strategic
considerations even if we believe we have sufficient funds for our
current or future operating plans. To the extent that additional
capital is raised through the sale of equity or convertible debt
securities, the issuance of these securities could result in
further dilution to our stockholders.
PLAN OF
DISTRIBUTION
Roth Capital Partners, LLC has agreed to act as placement agent in
connection with this offering subject to the terms and conditions
of the placement agency agreement dated February 16, 2021. Roth
Capital Partners, LLC is not purchasing or selling any of the
shares of our common stock offered by this prospectus supplement,
nor is it required to arrange the purchase or sale of any specific
number or dollar amount of shares of our common stock, but has
agreed to use its reasonable best efforts to arrange for the sale
of all of the shares of our common stock offered hereby.
Therefore, we will enter into a securities purchase agreement
directly with investors in connection with this offering and we may
not sell the entire amount of shares of our common stock offered
pursuant to this prospectus supplement. Investors who do not enter
into a securities purchase agreement will rely solely on this
prospectus in connection with the purchase of our securities in
this offering. This agreement includes representations and
warranties by us and such purchasers.
Delivery of the shares of common stock offered hereby is expected
to take place on or about February 18, 2021, subject to
satisfaction of certain conditions.
We have agreed to pay the placement agent a cash fee equal to 5.0%
of the gross proceeds received from investors who purchase
securities in the offering. In addition, subject to FINRA Rule
5110(f)(2)(d)(i), we have also agreed to reimburse the placement
agent at closing up to a maximum aggregate amount of $50,000 for
expenses in connection with this offering.
|
|
Per
Share |
|
|
Total |
|
Offering price |
|
$ |
7.60 |
|
|
$ |
13,000,560.00 |
|
Placement agent
fees |
|
$ |
0.38 |
|
|
$ |
650,028.00 |
|
Proceeds, before
expenses, to us |
|
$ |
7.22 |
|
|
$ |
12,350,532.00 |
|
Because there is no minimum offering amount required as a condition
to closing in this offering, the actual offering amount, placement
agent fees, and proceeds to us, if any, are not presently
determinable and may be substantially less than the total maximum
offering amounts set forth above.
The placement agent may be deemed to be an underwriter within the
meaning of Section 2(a)(11) of the Securities Act, and any
commissions received by it and any profit realized on the resale of
the shares sold by it while acting as principal might be deemed to
be underwriting discounts or commissions under the Securities Act.
As an underwriter, the placement agent would be required to comply
with the requirements of the Securities Act and the Exchange Act,
including, without limitation, Rule 415(a)(4) under the
Securities Act and Rule 10b-5 and Regulation M under the
Exchange Act. These rules and regulations may limit the timing
of purchases and sales of shares by the placement agent acting as
principal. Under these rules and regulations, the placement
agent:
|
· |
may not engage in any stabilization activity in connection with
our securities; and |
|
· |
may not bid for or purchase any of our securities or attempt to
induce any person to purchase any of our securities, other than as
permitted under the Exchange Act, until it has completed its
participation in the distribution. |
Determination of Offering Price
The public offering price of the shares of common stock we are
offering was negotiated between us and the investors, in
consultation with the placement agent based on the trading of our
common stock prior to the offering, among other things. Other
factors considered in determining the public offering price of our
common stock we are offering include the history and prospects of
the Company, the stage of development of our business, our business
plans for the future and the extent to which they have been
implemented, an assessment of our management, general conditions of
the securities markets at the time of the offering and such other
factors as were deemed relevant.
Indemnification
We have agreed to indemnify the placement agent and certain other
persons against certain liabilities under the Securities Act
relating to or arising out of the placement agent’s activities
under the placement agency agreement. We have also agreed to
contribute to payments the placement agent may be required to make
in respect of such liabilities.
Electronic Distribution
This prospectus supplement and the accompanying prospectus may be
made available in electronic format on websites or through other
online services maintained by the placement agent, or by an
affiliate. Other than this prospectus supplement and the
accompanying prospectus in electronic format, the information on
the placement agent’s websites and any information contained in any
other website maintained by the placement agent is not part of this
prospectus supplement and the accompanying prospectus or the
registration statement of which this prospectus supplement and the
accompanying prospectus form a part, has not been approved and/or
endorsed by us or the placement agent, and should not be relied
upon by investors.
Lock-Up Agreements
Each of our directors and executive officers has entered into a
lock-up agreement with the Company in connection with this
offering. Under the lock-up agreements, from the date of the
lock-up agreements until ninety (90) days after the closing of this
offering, the directors and executive officers will not offer,
sell, contract to sell, hypothecate, pledge or otherwise dispose of
(or enter into any transaction which is designed to, or might
reasonably be expected to, result in the disposition (whether by
actual disposition or effective economic disposition due to cash
settlement or otherwise) by the director or executive officer),
directly or indirectly, or establish or increase a put equivalent
position or liquidate or decrease a call equivalent position within
the meaning of Section 16 of the Securities Exchange Act, with
respect to, any shares of the Company’s common stock or securities
convertible, exchangeable or exercisable into, shares of common
stock.
Passive Market Making
In connection with this offering, the placement agent may engage in
passive market making transactions in our common stock on the
Nasdaq Capital Market in accordance with Rule 103 of
Regulation M promulgated under the Exchange Act during a period
before the commencement of offers or sales of shares of our common
stock and extending through the completion of the distribution. A
passive market maker must display its bid at a price not in excess
of the highest independent bid of that security. If all independent
bids are lowered below the passive market maker’s bid, however,
that bid must then be lowered when specified purchase limits are
exceeded.
Other
From time to time, the placement agent and its respective
affiliates may in the future provide various investment banking,
financial advisory and other services to us and our affiliates for
which services they may receive customary fees. In the course of
their businesses, the placement agent and its respective affiliates
may actively trade our securities or loans for their own account or
for the accounts of customers, and, accordingly, the placement
agent and its respective affiliates may at any time hold long or
short positions in such securities or loans. Except for services
provided in connection with this offering, the placement agent has
not provided any investment banking or other financial services
during the 180-day period preceding the date of this prospectus
supplement and we do not expect to retain the placement agent to
perform any investment banking or other financial services for at
least 90 days after the date of this prospectus supplement.
The foregoing does not purport to be a complete statement of the
terms and conditions of the placement agency agreement and
securities purchase agreement. A copy of the placement agency
agreement and the form of securities purchase agreement with the
investors will be included as exhibits to our Current Report on
Form 8-K that will be filed with the SEC and incorporated by
reference into the Registration Statement of which this prospectus
supplement forms a part.
The transfer agent for our common stock to be issued in this
offering is American Stock Transfer & Trust Company,
LLC.
LEGAL MATTERS
The validity of the issuance of the securities offered hereby will
be passed upon for us by Winstead PC, Houston, Texas. Pryor Cashman
LLP, New York, New York is acting as counsel for the placement
agent in connection with this offering.
EXPERTS
The consolidated financial statements as of December 31, 2019
and 2018 and for the years then ended incorporated by reference in
this prospectus supplement have been so incorporated in reliance on
the report of BDO USA, LLP, an independent registered public
accounting firm, incorporated herein by reference, given on the
authority of said firm as experts in auditing and accounting.
WHERE YOU CAN FIND MORE
INFORMATION
We have filed with the SEC a registration statement on
Form S-3 under the Securities Act with respect to the
securities being offered hereby. This prospectus supplement and the
accompanying prospectus, which constitute a part of the
registration statement, do not contain all of the information set
forth in the registration statement or the exhibits and schedules
filed therewith. For further information about us and the
securities offered hereby, we refer you to the registration
statement and the exhibits filed thereto. Statements contained in
this prospectus supplement and the accompanying prospectus
regarding the contents of any contract or any other document that
is filed as an exhibit to the registration statement are not
necessarily complete, and each such statement is qualified in all
respects by reference to the full text of such contract or other
document filed as an exhibit to the registration statement.
We file annual, quarterly and current reports, proxy statements and
other information with the SEC. The SEC maintains an Internet site
that contains reports, proxy and information statements, and other
information regarding issuers that file electronically with the
SEC, including us. The SEC’s Internet site can be found
at http://www.sec.gov. In addition, we make available
on or through our Internet site copies of these reports as soon as
reasonably practicable after we electronically file or furnished
them to the SEC. Our Internet site can be found
at http://www.biopathholdings.com. The information
contained in, or that can be accessed through, our website is not
incorporated by reference in, and is not part of, this prospectus
supplement or the accompanying prospectus.
INFORMATION INCORPORATED
BY REFERENCE
We are incorporating by reference into this prospectus supplement
and the accompanying prospectus certain information that we file
with the SEC, which means that we are disclosing important
information to you by referring you to those documents. The
information incorporated by reference is deemed to be part of this
prospectus supplement and the accompanying prospectus, except for
information incorporated by reference that is superseded by
information contained in this prospectus supplement and the
accompanying prospectus. This means that you must look at all of
the SEC filings that we incorporate by reference to determine if
any statements in this prospectus supplement, the accompanying
prospectus or any document previously incorporated by reference
have been modified or superseded. This prospectus supplement
incorporates by reference the documents set forth below that we
have previously filed with the SEC:
|
· |
our
Annual Report on Form 10-K for the fiscal year ended
December 31, 2019; |
|
· |
our
Quarterly Reports on Form 10-Q for the quarters ended
March 31, June 30, and September 30, 2020; |
|
· |
our
Definitive Proxy Statement on Schedule 14A relating to our 2020
Annual Meeting of Stockholders, filed November 5,
2020; |
|
· |
our
Current Reports on Form 8-K filed with the SEC on
November 19, 2020; December 18, 2020; and
February 10, 2021; and |
|
· |
the
description of our common stock contained in Exhibit 4.17 to
our Annual Report on Form 10-K for
the fiscal year ended December 31, 2019. |
Any information in any of the foregoing documents will
automatically be deemed to be modified or superseded to the extent
that information in this prospectus supplement or in a later filed
document that is incorporated or deemed to be incorporated herein
by reference modifies or replaces such information.
We also incorporate by reference all documents we subsequently file
in the future pursuant to Section 13(a), 13(c), 14 or
15(d) of the Exchange Act after the date of this prospectus
supplement until the termination of the offering. These documents
include periodic reports, such as Annual Reports on Form 10-K,
Quarterly Reports on Form 10-Q and Current Reports on
Form 8-K (except, in any such case, the portions furnished and
not filed pursuant to Item 2.02, Item 7.01 or otherwise), as
well as any proxy statements.
We will provide to each person, including any beneficial owner, to
whom a prospectus supplement and accompanying prospectus are
delivered, without charge upon written or oral request, a copy of
any or all of the documents that are incorporated by reference into
this prospectus supplement and the accompanying prospectus but not
delivered with the prospectus supplement and accompanying
prospectus, including exhibits which are specifically incorporated
by reference into such documents. You may request a copy of these
filings at no cost, by writing to or telephoning us at the
following address:
Bio-Path Holdings, Inc.
Attention: Secretary
4710 Bellaire Boulevard, Suite 210
Bellaire, Texas 77401
(832) 742-1357
PROSPECTUS

$125,000,000
COMMON STOCK
PREFERRED STOCK
WARRANTS
UNITS
We may from time to time offer and sell up to $125,000,000 of
common stock, preferred stock, warrants to purchase common stock or
preferred stock or any combination of the foregoing, either
individually or in units, at prices and on terms described in one
or more supplements to this prospectus. We may also offer
securities as may be issuable upon conversion, redemption,
repurchase, exchange or exercise of any securities registered
hereunder, including any applicable anti-dilution provisions.
This prospectus provides the general terms of the securities we may
offer and the general manner in which these securities will be
offered. Each time we offer to sell securities, we will provide
specific terms related to such offers in a supplement to this
prospectus. The prospectus supplements may also add, update or
change information contained in this prospectus. Before you invest,
you should carefully read this prospectus and the applicable
prospectus supplement, as well the documents incorporated by
referenced in this prospectus. This prospectus may not be used to
consummate a sale of securities unless accompanied by the
applicable prospectus supplement.
Our common stock is currently listed on the Nasdaq Capital Market
under the symbol “BPTH.” On May 14, 2019, the last reported sales
price per share of our common stock on the Nasdaq Capital Market
was $18.00.
We will sell these securities directly, through agents, dealers or
underwriters as designated from time to time, or through a
combination of these methods. For additional information on the
methods of sale, you should refer to the section titled “Plan of
Distribution” in this prospectus. If any agents, dealers or
underwriters are involved in the sale of these securities, the
applicable prospectus supplement will set forth the names of the
agents, dealers or underwriters and any applicable fees,
commissions or discounts. The price to the public of such
securities and the net proceeds that we expect to receive from such
sale will also be set forth in a supplement to this prospectus.
Investing in our securities involves a high degree of risk.
Before making an investment decision, you should review carefully
and consider all of the information set forth in this prospectus,
the applicable prospectus supplement and the documents incorporated
by reference in this prospectus and applicable prospectus
supplement. See “Risk Factors” on page 4 of this prospectus and
under similar headings in the other documents that are incorporated
by reference into this prospectus.
Neither the Securities and Exchange Commission nor any state
securities commission has approved or disapproved of these
securities or determined if this prospectus is truthful or
complete. Any representation to the contrary is a criminal
offense.
The date of this prospectus is June 5, 2019
TABLE OF CONTENTS
ABOUT THIS PROSPECTUS
This prospectus is part of a registration statement on Form S-3
that we filed with the Securities and Exchange Commission (the
“SEC”) using a “shelf” registration process. Under this shelf
registration statement process, we may from time to time sell
common stock, preferred stock, warrants to purchase common stock or
preferred stock or any combination of the foregoing, either
individually or in units, in one or more offerings up to an
offering amount of $125,000,000. This prospectus provides you with
a general description of the securities we may offer and the
general manner in which these securities will be offered.
Each time we offer securities hereunder, we will provide specific
terms related to such offering in a supplement to this
prospectus.
The prospectus supplements may add, update or change any of the
information contained in this prospectus or in the documents that
we have incorporated by reference into this prospectus. We urge you
to read carefully this prospectus and the applicable prospectus
supplement, together with the information incorporated herein by
reference as described under the sections titled “Where You Can
Find More Information” and “Information Incorporated by Reference”
below. If there is any inconsistency between the information in
this prospectus and any prospectus supplement, you should rely on
the information contained in that prospectus supplement.
This prospectus may not be used to consummate a sale of
securities unless it is accompanied by a prospectus
supplement.
You should rely only on the information we have provided or
incorporated by reference in this prospectus and the applicable
prospectus supplement. We have not authorized anyone to provide you
with different information. No dealer, salesperson or other person
is authorized to give any information or to represent anything not
contained in this prospectus or the applicable prospectus
supplement. You must not rely on any unauthorized information or
representation. This prospectus or any applicable supplement to
this prospectus do not constitute an offer to sell or the
solicitation of an offer to buy any securities other than the
registered securities to which they relate, nor do this prospectus
or any applicable supplement to this prospectus constitute an offer
to sell or the solicitation of an offer to buy securities in any
jurisdiction to any person to whom it is unlawful to make such
offer or solicitation in such jurisdiction. You should assume that
the information in this prospectus is accurate only as of the date
on the front of the document and that any information we have
incorporated by reference is accurate only as of the date of the
document incorporated by reference. Our business, financial
condition, results of operations and prospects may have changed
since those dates.
This prospectus contains summaries of certain provisions contained
in some of the documents described herein, but reference is made to
the actual documents for complete information. All of the summaries
are qualified in their entirety by the actual documents. Copies of
some of the documents referred to herein have been filed, will be
filed or will be incorporated by reference as exhibits to the
registration statement of which this prospectus is a part, and you
may obtain copies of those documents as described below under the
section titled “Where You Can Find More Information.”
Unless the context requires otherwise, references in this
prospectus to “we,” “our,” “us,” “the Company” and “Bio-Path” refer
to Bio-Path Holdings, Inc. and its wholly-owned subsidiary.
Bio-Path Holdings, Inc.’s wholly-owned subsidiary, Bio-Path, Inc.,
is sometimes referred to herein as “Bio-Path Subsidiary.”
PROSPECTUS SUMMARY
This prospectus summary highlights selected information
contained elsewhere in this prospectus or in documents incorporated
by reference. This summary does not contain all of the information
that you should consider before making an investment decision. You
should carefully read the entire prospectus, the applicable
prospectus supplement, including under the section titled “Risk
Factors” and the documents incorporated by reference into this
prospectus, before making an investment decision.
Our Company
We are a clinical and preclinical stage oncology focused RNAi
nanoparticle drug development company utilizing a novel technology
that achieves systemic delivery for target specific protein
inhibition for any gene product that is over-expressed in disease.
Our drug delivery and antisense technology, called DNAbilize®, is a
platform that uses P-ethoxy, which is a deoxyribonucleic acid (DNA)
backbone modification that is intended to protect the DNA from
destruction by the body’s enzymes when circulating in vivo,
incorporated inside of a neutral charged lipid bilayer. We believe
this combination allows for high efficiency loading of antisense
DNA into non-toxic, cell-membrane-like structures for delivery of
the antisense drug substance into cells. In vivo, the
DNAbilize® delivered antisense drug substances are systemically
distributed throughout the body to allow for reduction or
elimination of target proteins in blood diseases and solid tumors.
Through testing in numerous animal studies and treatment in over 70
patients, the Company’s DNAbilize® drug candidates have
demonstrated an excellent safety profile. DNAbilize® is a
registered trademark of the Company.
Using DNAbilize® as a platform for drug development and
manufacturing, we currently have three antisense drug candidates in
development to treat at least five different cancer disease
indications. Our lead drug candidate, prexigebersen (pronounced
prex” i je ber’ sen), is in the efficacy portion of a Phase 2
clinical trial for acute myeloid leukemia (AML) in combination with
low-dose cytarabine (LDAC) and in combination with decitabine. On
March 6, 2019, we announced intended amendments to this Phase 2
clinical trial to, among other things, add prexigebersen in
combination with decitabine for myelodysplastic syndrome and close
prexigebersen in combination with LDAC. In addition, preclinical
efficacy studies are underway for triple combination prexigebersen,
decitabine and Venclexta in AML. Prexigebersen is also being
studied in the safety portion of a Phase 2a clinical trial for
chronic myeloid leukemia in combination with dasatinib.
Prexigebersen was shown to enhance chemotherapy efficacy in
preclinical solid tumor models, such as ovarian cancer, and we
intend to file an Investigational New Drug (IND) application for
prexigebersen in solid tumors in 2019.
Our second drug candidate, Liposomal Bcl-2 (“BP1002”), targets the
protein Bcl-2, which is responsible for driving cell survival in up
to 60% of all cancers. We are currently preparing an IND
application for BP1002 after completing additional IND enabling
studies. We intend to initiate a Phase 1 clinical trial of BP1002
in refractory/relapsed lymphoma and chronic lymphocytic leukemia
patients once we receive approval from the U.S. Food and Drug
Administration (FDA).
Our third drug candidate, Liposomal Stat3 (“BP1003”), targets the
Stat3 protein and is currently in preclinical development as a
potential treatment of pancreatic cancer, non-small cell lung
cancer (NSCLC) and AML. Preclinical models have shown BP1003 to
inhibit cell viability and STAT3 protein expression in NSCLC and
AML cell lines. Further, BP1003 successfully penetrated pancreatic
tumors and significantly enhanced the efficacy of gemcitabine, a
treatment for patients with advanced pancreatic cancer, in a
pancreatic patient derived tumor model. Our lead indication for
BP1003 is pancreatic cancer due to the severity of this disease and
the lack of effective, life-extending treatments. We intend to
complete IND enabling studies of BP1003 in 2019 and to file an IND
application for a Phase 1 clinical trial of BP1003 for the
treatment of solid tumors, including pancreatic cancer in 2020.
Our DNAbilize® technology-based products are available for
out-licensing or partnering. We intend to apply our drug delivery
technology template to new disease-causing protein targets as a
means to develop new nanoparticle antisense RNAi drug candidates.
We have a new product identification template in place to define a
process of scientific, preclinical, commercial and intellectual
property evaluation of potential new drug candidates for inclusion
into our drug product development pipeline. As we expand, we will
look at indications where a systemic delivery is needed and
antisense RNAi nanoparticles can be used to slow, reverse or cure a
disease, either alone or in combination with another drug. On July
19, 2017, we announced that the United States Patent and Trademark
Office issued a notice of allowance for claims related to
DNAbilize®, including its use in the treatment of cancers,
autoimmune diseases and infectious diseases.
We have certain intellectual property as the basis for our current
drug products in clinical development, specifically prexigebersen,
BP1002 and BP1003. We are developing RNAi antisense nanoparticle
drug candidates based on our own patented technology to treat
cancer and autoimmune disorders where targeting a single protein
may be advantageous and result in reduced patient adverse effects
as compared to small molecule inhibitors with off-target and
non-specific effects. We have composition of matter and method of
use intellectual property for the design and manufacture of
antisense RNAi nanoparticle drug products.
Corporate Information
The Company was incorporated in May 2000 as a Utah corporation. In
February 2008, Bio-Path Subsidiary completed a reverse merger with
the Company, which at the time was traded over the counter and had
no current operations. The prior name of the Company was changed to
Bio-Path Holdings, Inc. and the directors and officers of Bio-Path
Subsidiary became the directors and officers of Bio-Path Holdings,
Inc. On March 10, 2014, our common stock ceased trading on the
OTCQX and commenced trading on the Nasdaq Capital Market under the
ticker symbol “BPTH.” Effective December 31, 2014, we changed our
state of incorporation from Utah to Delaware through a statutory
conversion pursuant to the Utah Revised Business Corporation Act
and the Delaware General Corporation Law. Our principal executive
offices are located at 4710 Bellaire Boulevard, Suite 210,
Bellaire, Texas 77401, and our telephone number is (832)
742-1357.
On February 8, 2018, we effected a reverse stock split of our
outstanding shares of common stock at a ratio of 1-for-10, and our
common stock began trading on the split-adjusted basis on the
Nasdaq Capital Market at the commencement of trading on February 9,
2018. In addition, on January 17, 2019, we effected a reverse stock
split of our outstanding shares of common stock at a ratio of
1-for-20, and our common stock began trading on the split-adjusted
basis on the Nasdaq Capital Market at the commencement of trading
on January 18, 2019. All common stock share and per share amounts
in this prospectus have been adjusted to give effect to both the
1-for-10 reverse stock split and the 1-for-20 reverse stock split,
retrospectively.
THE OFFERING
We may offer common stock, preferred stock, warrants to purchase
common stock or preferred stock or any combination of the
foregoing, either individually or in units, in one or more
offerings, with an aggregate initial offering price not to exceed
$125,000,000. This prospectus describes the general terms that may
apply to the securities to be offered and the specific terms of any
particular securities that we offer will be described in a separate
supplement to this prospectus, including, to the extent
applicable:
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designation or
classification; |
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aggregate offering
price; |
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rates and times of payment of
dividends, if any; |
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redemption, conversion, exchange
or sinking fund terms, if any; |
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restrictive covenants, if
any; |
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voting or other rights, if
any; |
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conversion, exchange and exercise
prices, if any; and |
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important federal income tax
considerations. |
We may offer and sell the securities directly, through agents,
dealers or underwriters as designated from time to time, or through
a combination of these methods. The applicable prospectus
supplement will include any required information about the agents,
dealers or underwriters we use and the applicable fees, commissions
or discounts we may pay them for their services.
This prospectus may not be used to consummate a sale of
securities unless it is accompanied by a prospectus
supplement.
RISK FACTORS
An investment in our company involves a high degree of risk. Before
you make a decision to invest in our securities, you should
consider carefully the risks described in or incorporated by
reference in this prospectus, including the risks and uncertainties
discussed under the section titled “Risk Factors” in our most
recent Annual Report on Form 10-K and any subsequent Quarterly
Reports on Form 10-Q or Current Reports on Form 8-K, and all other
documents incorporated by reference into this prospectus, as
updated by our subsequent filings under the Securities Exchange Act
of 1934, as amended (the “Exchange Act”), and the risk factors and
other information contained in the applicable prospectus
supplement.
Any of these risks could have a material adverse effect on our
business, prospects, financial condition and results of operations.
In any such case, the trading price of our securities could decline
and you could lose all or part of your investment. Additional risks
not presently known to us or that we currently deem immaterial may
also adversely affect our business operations.
SPECIAL NOTE REGARDING
FORWARD-LOOKING STATEMENTS
This prospectus and the documents incorporated by reference into
this prospectus contain “forward-looking statements” within the
meaning of Section 27A of the Securities Act of 1933, as amended
(the “Securities Act”), and Section 21E of the Exchange Act.
Forward-looking statements can be identified by words such as
“anticipate,” “expect,” “intend,” “plan,” “believe,” “seek,”
“estimate,” “project,” “goal,” “strategy,” “future,” “likely,”
“may,” “should,” “will” and variations of these words and similar
references to future periods, although not all forward-looking
statements contain these identifying words. Forward-looking
statements are neither historical facts nor assurances of future
performance. Instead, they are based on our current beliefs,
expectations and assumptions regarding the future of our business,
future plans and strategies, projections, anticipated events and
trends, the economy and other future conditions. Because
forward-looking statements relate to the future, they are subject
to inherent risks, uncertainties, and changes in circumstances,
including but not limited to risk factors contained in or
incorporated by reference under the section titled, “Risk Factors.”
As a result, our actual results may differ materially from those
expressed or forecasted in the forward-looking statements, and you
should not rely on such forward-looking statements. You should
carefully read this prospectus and any applicable supplement to
this prospectus, together with the information incorporated herein
by reference as described under the section titled “Where You Can
Find More Information,” completely and with the understanding that
our actual future results may be materially different from what we
expect. We can give no assurances that any of the events
anticipated by the forward-looking statements will occur or, if any
of them do, what impact they will have on our results of operations
and financial condition. Forward-looking statements include, but
are not limited to, statements about:
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our lack of significant revenue
to date, our history of recurring operating losses and our
expectation of future operating losses; |
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our need for substantial
additional capital and our need to delay, reduce or eliminate our
drug development and commercialization efforts if we are unable to
raise additional capital; |
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the highly-competitive nature of
the pharmaceutical and biotechnology industry and our ability to
compete effectively; |
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the success of our plans to use
collaboration arrangements to leverage our
capabilities; |
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our ability to retain and attract
key personnel; |
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the risk of misconduct of our
employees, agents, consultants and commercial partners; |
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disruptions to our operations due
to expansions of our operations; |
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the costs we would incur if we
acquire or license technologies, resources or drug
candidates; |
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risks associated with product
liability claims; |
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our reliance on information
technology systems and the liability or interruption associated
with cyber-attacks or other breaches of our systems; |
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our ability to use net operating
loss carryforwards; |
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provisions in our charter
documents and state law that may prevent a change in
control; |
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work slowdown or stoppage at
government agencies could negatively impact our
business |
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our need to complete extensive
clinical trials and the risk that we may not be able to demonstrate
the safety and efficacy of our drug candidates; |
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risks that that our clinical
trials may be delayed or terminated; |
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our ability to obtain domestic
and foreign regulatory approval for our drug
candidates; |
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changes in existing laws and
regulations affecting the healthcare industry; |
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our reliance on third parties to
conduct clinical trials for our drug candidates; |
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our ability to maintain orphan
drug exclusivity for our drug candidates; |
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our reliance on third parties for
manufacturing our clinical drug supplies; |
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risks associated with the
manufacture of our drug candidates; |
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our ability to establish sales
and marketing capabilities relating to our drug
candidates; |
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market acceptance of our drug
candidates; |
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third-party payor reimbursement
practices; |
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our ability to adequately protect
the intellectual property of our drug candidates; |
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infringement on the intellectual
property rights of third parties; |
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costs and time relating to
litigation regarding intellectual property rights; |
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our ability to adequately prevent
disclosure by our employees or others of trade secrets and other
proprietary information; |
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the volatility of the trading
price of our common stock; |
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our common stock being thinly
traded; |
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our ability to issue shares of
common or preferred stock without approval from our
stockholders; |
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our ability to pay cash
dividends; |
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costs and expenses associated
with being a public company; |
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a material weakness identified in
our internal controls over financial reporting; and |
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our ability to maintain
compliance with the listing standards of the Nasdaq Capital
Market. |
Any forward-looking statement made by us in this prospectus, any
applicable supplement to this prospectus and the documents
incorporated by reference into this prospectus is based only on
information currently available to us and speaks only as of the
date on which it is made. We undertake no obligation to publicly
update any forward-looking statement, whether as a result of new
information, future developments or otherwise. However, you should
carefully review the risk factors set forth in other reports or
documents we file from time to time with the SEC.
USE OF PROCEEDS
Unless otherwise indicated in the applicable prospectus supplement,
we expect to use the net proceeds from the sale of securities
offered pursuant to this prospectus for working capital and general
corporate purposes. Until the net proceeds are used for these
purposes, we may deposit them in interest-bearing accounts or
invest them in short-term marketable securities.
DESCRIPTION OF CAPITAL
STOCK
The following description of our common stock and preferred stock
is a summary. It is not complete and is subject to and qualified in
its entirety by our certificate of incorporation and first amended
and restated bylaws, each of which is incorporated by reference
into this prospectus. See the sections titled
“Where You Can Find More Information” and “Information Incorporated
by Reference.” As of the date of this prospectus, our certificate
of incorporation authorizes us to issue 200,000,000 shares of
common stock, par value $0.001 per share, and 10,000,000 shares of
preferred stock, par value $0.001 per share. As of May 7, 2019,
there were 2,831,356 shares of common stock issued and outstanding
and no shares of preferred stock issued and outstanding.
Common Stock
Holders of common stock are entitled to one vote for each share
held in the election of directors and on all other matters
submitted to a vote of stockholders. Cumulative voting of shares of
common stock is prohibited. Accordingly, holders of a majority of
the shares of common stock entitled to vote in any election of
directors may elect all of the directors standing for election.
Subject to the prior rights of the holders of any outstanding
preferred stock, holders of common stock are entitled to receive
dividends when, as and if declared by our board of directors out of
funds legally available therefor. Upon the liquidation, dissolution
or winding up of our company, the holders of common stock are
entitled to receive ratably the assets of our company remaining
after payment of all liabilities and payment to holders of
preferred stock if such preferred stock has an involuntary
liquidation preference over the common stock. Holders of common
stock have no preemptive, subscription, redemption or conversion
rights. The outstanding shares of common stock are, and the shares
offered by us in this offering will be, when issued and paid for,
validly issued, fully paid and nonassessable.
As of March 31, 2019, there were approximately 227 holders of
record of our common stock.
Preferred Stock
Our board of directors is authorized, without any further notice to
or action of the stockholders, to issue up to 10,000,000 shares of
preferred stock in one or more series. Our board of directors is
further authorized, subject to limitations prescribed by law, to
fix by resolution or resolutions the designations, powers,
preferences and rights, and the qualifications, limitations or
restrictions thereof, of any wholly unissued series of our
preferred stock, including without limitation authority to fix by
resolution or resolutions the dividend rights, dividend rate,
conversion rights, voting rights, rights and terms of redemption
(including sinking fund provisions), redemption price or prices,
and liquidation preferences of any such series, and the number of
shares constituting any such series and the designation thereof, or
any of the foregoing. The board of directors is further authorized
to increase (but not above the total number of authorized shares of
the class) or decrease (but not below the number of shares of any
such series then outstanding) the number of shares of any series,
the number of which was fixed by it, subsequent to the issuance of
shares of such series then outstanding, subject to the powers,
preferences and rights, and the qualifications, limitations and
restrictions thereof stated in our certificate of incorporation or
the resolution of our board of directors originally fixing the
number of shares of such series. If the number of shares of any
series is so decreased, then the shares constituting such decrease
shall resume the status which they had prior to the adoption of the
resolution originally fixing the number of shares of such series.
As of the date of this prospectus, no such shares had been
designated.
The following briefly summarizes the material terms of preferred
stock that we may offer, other than pricing and related terms
disclosed in a prospectus supplement. You should read the
particular terms of any series of preferred stock that we offer
which we will describe in more detail in the applicable prospectus
supplement relating to such series. You should also read the more
detailed provisions of our certificate of incorporation and the
statement with respect to shares relating to each particular series
of preferred stock for provisions that may be important to you. The
statement with respect to shares relating to each particular series
of preferred stock offered by the applicable prospectus supplement
and this prospectus will be filed as an exhibit to a document
incorporated by reference in the prospectus. The prospectus
supplement will also state whether any of the terms summarized
below do not apply to the series of preferred stock being
offered.
Rank. A series of preferred stock will have the rank set
forth in the relevant certificate of designation and described in
the prospectus supplement relating to the applicable series.
Voting Rights. The holders of shares of a series of
preferred stock will have the voting rights provided by the
applicable certificate of designation and as required by applicable
law. These voting rights will be described in the relevant
prospectus supplement.
Dividends. The certificate of designation setting forth the
terms of a series of preferred stock may provide that the holders
of that series are entitled to receive dividends, when, as and if
authorized by our board of directors out of funds legally available
for dividends, before any declaration or payment of any dividends
on securities ranking junior to such series relating to dividends.
The rates and dates of payment of dividends and any other terms
applicable to the dividends will be set forth in the applicable
certificate of designation and described in the prospectus
supplement relating to the relevant series. To the extent provided
in the certificate of designation, dividends will be payable to the
holders of record of our preferred stock as they appear on our
books on the record dates fixed by our board of directors.
Dividends on any series of our preferred stock may be cumulative or
noncumulative and payable in cash or in kind.
Conversion and Exchange. The certificate of designation
setting forth the terms of a series of our preferred stock may
provide for, and the prospectus supplement for the applicable
series of preferred stock may describe, the terms, if any, on which
shares of that series are convertible into or exchangeable for
shares of our common stock or securities of a third party.
Redemption. If so specified in the certificate of
designation setting forth the terms of a series of our preferred
stock, which will be described in the applicable prospectus
supplement, a series of our preferred stock may be redeemable at
our or the holder’s option and/or may be mandatorily redeemed
partially or in whole.
Liquidation Preference. Upon any voluntary or involuntary
liquidation, dissolution or winding up of our company, the holders
of each series of our preferred stock may be entitled to receive
distributions upon liquidation. Those distributions will be made
before any distribution is made on any securities ranking junior to
such series relating to liquidation. The terms and conditions of
those distributions to the relevant series of our preferred stock
will be set forth in the applicable certificate of designation and
described in the relevant prospectus supplement.
Our board of directors may cause shares of preferred stock to be
issued in public or private transactions for any proper corporate
purposes, and such issuance could adversely affect the voting
rights of the holders of our common stock. The issuance of our
preferred stock could also affect the likelihood that the holders
of common stock will receive dividends or distributions upon
liquidation. In addition, the rights of the holders of the
preferred stock offered may be adversely affected by the rights of
the holders of any shares of our preferred stock that may be issued
in the future. The preferred stock could have the effect of acting
as an anti-takeover device to prevent a change in control of our
company.
Unless the particular prospectus supplement states otherwise, the
holders of each series of our preferred stock will not have any
preemptive or subscription rights to acquire more of our capital
stock.
The transfer agent, registrar, dividend disbursing agent and
redemption agent for shares of each series of preferred stock will
be named in the prospectus supplement relating to such series.
Limitation on Liability and Indemnification of Officers and
Directors
Our certificate of incorporation and first amended and restated
bylaws provide for indemnification of our officers and directors to
the fullest extent permitted by Delaware law. Our certificate of
incorporation and first amended and restated bylaws limit the
liability of our directors for monetary damages to the fullest
extent permitted by Delaware law. We maintain directors’ and
officers’ liability insurance.
Anti-Takeover Effects of Provisions of Our Certificate of
Incorporation, Our Bylaws and Delaware Law
Some provisions of Delaware law and our certificate of
incorporation and our first amended and restated bylaws contain
provisions that could have the effect of delaying, deterring or
preventing another party from acquiring or seeking to acquire
control of us. These provisions are intended to discourage certain
types of coercive takeover practices and inadequate takeover bids
and to encourage anyone seeking to acquire control of us to
negotiate first with our board of directors. However, these
provisions may also delay, deter or prevent a change in control or
other takeover of our company that our stockholders might consider
to be in their best interests, including transactions that might
result in a premium being paid over the market price of our common
stock and also may limit the price that investors are willing to
pay in the future for our common stock. These provisions may also
have the effect of preventing changes in our management.
Our certificate of incorporation and first amended and restated
bylaws include anti-takeover provisions that:
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authorize our board of directors,
without further action by the stockholders, to issue shares of
preferred stock in one or more series, and with respect to each
series, to fix the number of shares constituting that series and
establish the rights and other terms of that series; |
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establish advance notice
procedures for stockholders to submit nominations of candidates for
election to our board of directors and other proposals to be
brought before a stockholders meeting; |
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provide that our first amended
and restated bylaws may be amended by our board of directors
without stockholder approval; |
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limit our stockholders’ ability
to call special meetings of stockholders; |
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allow our directors to establish
the size of the board of directors by action of the board, subject
to a minimum of three members; |
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provide that vacancies on our
board of directors or newly created directorships resulting from an
increase in the number of our directors may be filled only by a
majority of directors then in office, even though less than a
quorum; and |
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do not give the holders of our
common stock cumulative voting rights with respect to the election
of directors. |
Business Combinations
Section 203 of the Delaware General Corporation Law provides that
we may not engage in certain “business combinations” with any
“interested stockholder” for a three-year period following the time
that the person became an interested stockholder, unless:
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prior to the time that person
became an interested stockholder, our board of directors approved
either the business combination or the transaction which resulted
in the person becoming an interested stockholder; |
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upon consummation of the
transaction which resulted in the person becoming an interested
stockholder, the interested stockholder owned at least 85% of the
voting stock of the corporation outstanding at the time the
transaction commenced, excluding certain shares; or |
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at or subsequent to the time the
person became an interested stockholder, the business combination
is approved by the board of directors and by the affirmative vote
of at least 66 2/3% of the outstanding voting stock which is not
owned by the interested stockholder. |
Generally, a business combination includes a merger, consolidation,
asset or stock sale or other transaction resulting in a financial
benefit to the interested stockholder. Subject to certain
exceptions, an interested stockholder is a person who, together
with that person’s affiliates and associates, owns, or within the
previous three years owned, 15% or more of our voting stock. The
statute could prohibit or delay mergers or other takeover or change
in control attempts with respect to us and, accordingly, may
discourage attempts to acquire us.
Listing
Our common stock is listed for trading on the Nasdaq Capital Market
under the symbol “BPTH.”
Transfer Agent and Registrar
The transfer agent and registrar for our common stock is American
Stock Transfer & Trust Company, LLC, 6201 15th
Avenue, Brooklyn, New York 11219. Its phone number is (800)
937-5449.
DESCRIPTION OF
WARRANTS
The following description, together with the additional information
we include in the applicable prospectus supplement, summarizes the
material terms and provisions of the warrants that we may offer
under this prospectus. We may issue warrants for the purchase of
shares of common stock and/or preferred stock. We may issue
warrants independently or together with shares of common stock
and/or shares of preferred stock, and the warrants may be attached
to or separate from these securities. While the terms summarized
below will apply generally to any warrants that we may offer, we
will describe the particular terms of any series of warrants in
more detail in the applicable prospectus supplement. The terms of
any warrants offered under a prospectus supplement may differ from
the terms described below.
Before the issuance of a series of warrants, the form of warrant
agreement, including a form of warrant certificate, if applicable,
that describes the terms of the particular series of warrants we
are offering will be filed as an exhibit to the registration
statement of which this prospectus is a part, or incorporated by
reference from reports that we file with the SEC. The following
summaries of material provisions of the warrants are subject to,
and qualified in their entirety by reference to, all the provisions
of the warrant agreement and warrant certificate applicable to the
particular series of warrants that we may offer under this
prospectus and the applicable prospectus supplement. We urge you to
read the applicable prospectus supplements related to the
particular series of warrants that we may offer under this
prospectus, as well as any related free writing prospectuses, and
the complete warrant agreements and warrant certificates that
contain the terms of the warrants.
General
We will describe in the applicable prospectus supplement the terms
of the warrants that may be offered, including the following, where
applicable:
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the title of the
warrants; |
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• |
the aggregate number of the
warrants offered; |
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• |
the price or prices at which the
warrants will be issued; |
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• |
the securities, which may include
shares of any class or series of common stock or preferred stock,
for which the warrants are exercisable; |
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• |
in the case of warrants to
purchase common stock or preferred stock, the number of shares of
common stock or preferred stock, as the case may be, purchasable
upon the exercise of one warrant and the price at which these
shares may be purchased upon such exercise; |
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• |
the terms of any rights to redeem
or call the warrants; |
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• |
the date on and after which the
warrants and the related securities will be separately
transferable; |
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• |
the effect of any merger,
consolidation, sale or other disposition of our business on the
warrant agreements and the warrants; |
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• |
the terms of any rights to force
the exercise of the warrants; |
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• |
the dates on which the right to
exercise the warrants will commence and the date on which the right
will expire; |
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• |
the minimum or maximum number of
warrants that may be exercised at any one time; |
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• |
the manner in which the warrant
agreements and warrants may be modified; |
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• |
any provisions for changes to or
adjustments in the exercise price or number of securities issuable
upon exercise of the warrants; |
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information relating to
book-entry procedures; |
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• |
the listing of the warrants on a
securities exchange or automated quotation system; |
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• |
whether the warrants may be sold
separately or with other securities as parts of units; |
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• |
a discussion of material United
States federal income tax considerations of holding or exercising
the warrants; and |
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any other terms of the warrants,
including terms, procedures and limitations relating to the
exchange and exercise of the warrants. |
Before exercising their warrants, the holders of warrants will not
have any of the rights of the holders of the securities purchasable
upon such exercise, including the right to receive dividends, if
any, or, payments upon our liquidation, dissolution or winding up
or to exercise voting rights, if any.
Exercise of Warrants
Each warrant will entitle the holder to purchase the securities
that we specify in the applicable prospectus supplement at the
exercise price that we describe in the applicable prospectus
supplement. Unless we otherwise specify in the applicable
prospectus supplement, the holders of the warrants may exercise the
warrants at any time up to the specified time on the expiration
date that we set forth in the applicable prospectus supplement.
After the close of business on the expiration date, unexercised
warrants will become void.
Unless we otherwise specify in the applicable prospectus
supplement, the holders of the warrants may exercise the warrants
by delivering the warrant certificate representing the warrants to
be exercised together with specified information, and paying the
required amount to us or to the warrant agent in immediately
available funds, or, if provided in the applicable prospectus
supplement, by cashless exercise. We will set forth in the warrant
agreement, on the reverse side of the warrant certificate and in
the applicable prospectus supplement the information that the
holder of the warrant will be required to deliver to the warrant
agent in connection with the exercise of the warrant.
Unless we otherwise specify in the applicable prospectus
supplement, upon receipt of the required exercise price and the
warrant certificate properly completed and duly executed at the
corporate trust office of the warrant agent or any other office
indicated in the applicable prospectus supplement, we will issue
and deliver the securities purchasable upon such exercise. If fewer
than all of the warrants represented by the warrant certificate are
exercised, then we may issue a new warrant certificate for the
remaining amount of warrants. If we so indicate in the applicable
prospectus supplement, the holders of the warrants may surrender
securities as all or part of the exercise price for warrants.
Enforceability of Rights by Holders of Warrants
Any warrant agent will act solely as our agent under the applicable
warrant agreement and will not assume any obligation or
relationship of agency or trust with any holder of any warrant. A
single bank or trust company may act as warrant agent for more than
one issue of warrants. A warrant agent will have no duty or
responsibility in case of any default by us under the applicable
warrant agreement or warrant, including any duty or responsibility
to initiate any proceedings at law or otherwise, or to make any
demand upon us. Any holder of a warrant may, without the consent of
any related warrant agent or the holder of any other warrant,
enforce by appropriate legal action its right to exercise, and
receive the securities purchasable upon exercise of, its
warrants.
Warrant Adjustments
Unless the applicable prospectus supplement states otherwise, the
exercise price of, and the number of securities covered by, a
warrant to purchase shares of common stock or preferred stock will
be adjusted proportionately if we subdivide or combine common stock
or preferred stock, as applicable.
Warrant Agreement Will Not Be Qualified Under Trust Indenture
Act
No warrant agreement will be qualified as an indenture, and no
warrant agent will be required to qualify as a trustee, under the
Trust Indenture Act. Therefore, holders of warrants issued under a
warrant agreement will not have the protection of the Trust
Indenture Act with respect to their warrants.
Currently Outstanding Warrants
As of May 7, 2019, we had issued and outstanding warrants to
purchase 256,564 shares of our common stock with a weighted
exercise price of $37.43 per share.
DESCRIPTION OF UNITS
The following description, together with the additional information
we may include in any applicable prospectus supplements, summarizes
the material terms and provisions of the units that we may offer
under this prospectus. While the terms we have summarized below
will apply generally to any units that we may offer under this
prospectus, we will describe the particular terms of any series of
units in more detail in the applicable prospectus supplement. The
terms of any units offered under a prospectus supplement may differ
from the terms described below. However, no prospectus supplement
will fundamentally change the terms that are set forth in this
prospectus or offer a security that is not registered and described
in this prospectus at the time of its effectiveness.
Before the issuance of units, the form of unit agreement that
describes the terms of the series of units we are offering, and any
supplemental agreements, will be filed as an exhibit to the
registration statement of which this prospectus is a part, or
incorporated by reference from reports that we file with the SEC.
The following summaries of material terms and provisions of the
units are subject to, and qualified in their entirety by reference
to, all the provisions of the unit agreement and any supplemental
agreements applicable to a particular series of units. We urge you
to read the applicable prospectus supplements related to the
particular series of units that we sell under this prospectus, as
well as any related free writing prospectuses, and the complete
unit agreement and any supplemental agreements that contain the
terms of the units.
General
We may issue units consisting of common stock, preferred stock
and/or warrants in any combination. Each unit will be issued so
that the holder of the unit is also the holder of each security
included in the unit. Thus, the holder of a unit will have the
rights and obligations of a holder of each included security. The
unit agreement under which a unit is issued may provide that the
securities included in the unit may not be held or transferred
separately, at any time or at any time before a specified date.
We will describe in the applicable prospectus supplement the terms
of the series of units, including:
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the designation and terms of the
units and of the securities comprising the units, including whether
and under what circumstances those securities may be held or
transferred separately; |
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• |
any provisions of the governing
unit agreement that differ from those described below;
and |
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• |
any provisions for the issuance,
payment, settlement, transfer or exchange of the units or of the
securities comprising the units. |
The provisions described in this section, as well as those
described under “Description of Capital Stock” and “Description of
Warrants” will apply to each unit and to any common stock,
preferred stock and/or warrant included in each unit,
respectively.
Issuance in Series
We may issue units in such amounts and in numerous distinct series
as we determine.
Enforceability of Rights by Holders of Units
Any unit agent will act solely as our agent under the applicable
unit agreement and will not assume any obligation or relationship
of agency or trust with any holder of any unit. A single bank or
trust company may act as unit agent for more than one series of
units. A unit agent will have no duty or responsibility in case of
any default by us under the applicable unit agreement or unit,
including any duty or responsibility to initiate any proceedings at
law or otherwise, or to make any demand upon us. Any holder of a
unit may, without the consent of the related unit agent or the
holder of any other unit, enforce by appropriate legal action its
rights as holder under any security included in the unit.
LEGAL OWNERSHIP OF
SECURITIES
We can issue securities in registered form or in the form of one or
more global securities. We describe global securities in greater
detail below. We refer to those persons who have securities
registered in their own names on the books that we or any
applicable trustee, depositary or warrant or unit agent maintain
for this purpose as the “holders” of those securities. These
persons are the legal holders of the securities. We refer to those
persons who, indirectly through others, own beneficial interests in
securities that are not registered in their own names as “indirect
holders” of those securities. As we discuss below, indirect holders
are not legal holders and investors in securities issued in
book-entry form or in street name will be indirect holders.
Book-Entry Holders
We may issue securities in book-entry form only, as we will specify
in the applicable prospectus supplement. This means securities may
be represented by one or more global securities registered in the
name of a financial institution that holds them as depositary on
behalf of other financial institutions that participate in the
depositary’s book-entry system. These participating institutions,
which are referred to as participants, in turn, hold beneficial
interests in the securities on behalf of themselves or their
customers.
Only the person in whose name a security is registered is
recognized as the holder of that security. Securities issued in
global form will be registered in the name of the depositary or its
participants. Consequently, for securities issued in global form,
we will recognize only the depositary as the holder of the
securities, and we will make all payments on the securities to the
depositary. The depositary passes along the payments it receives to
its participants, which in turn pass the payments along to their
customers who are the beneficial owners. The depositary and its
participants do so under agreements they have made with one another
or with their customers; they are not obligated to do so under the
terms of the securities.
As a result, investors in a book-entry security will not own
securities directly. Instead, they will own beneficial interests in
a global security, through a bank, broker or other financial
institution that participates in the depositary’s book-entry system
or holds an interest through a participant. As long as the
securities are issued in global form, investors will be indirect
holders, and not holders, of the securities.
Street Name Holders
We may terminate a global security or issue securities in
non-global form. In these cases, investors may choose to hold their
securities in their own names or in “street name.” Securities held
by an investor in street name would be registered in the name of a
bank, broker or other financial institution that the investor
chooses, and the investor would hold only a beneficial interest in
those securities through an account he or she maintains at that
institution.
For securities held in street name, we or any applicable trustee or
depositary will recognize only the intermediary banks, brokers and
other financial institutions in whose names the securities are
registered as the holders of those securities, and we or any such
trustee or depositary will make all payments on those securities to
them. These institutions pass along the payments they receive to
their customers who are the beneficial owners, but only because
they agree to do so in their customer agreements or because they
are legally required to do so. Investors who hold securities in
street name will be indirect holders, not holders, of those
securities.
Legal Holders
Our obligations, as well as the obligations of any applicable
trustee and of any third parties employed by us or a trustee, run
only to the legal holders of the securities. We do not have
obligations to investors who hold beneficial interests in global
securities, in street name or by any other indirect means. This
will be the case whether an investor chooses to be an indirect
holder of a security or has no choice because we are issuing the
securities only in global form.
For example, once we make a payment or give a notice to the holder,
we have no further responsibility for the payment or notice even if
that holder is required, under agreements with depositary
participants or customers or by law, to pass it along to the
indirect holders but does not do so.
Special Considerations for Indirect Holders
If you hold securities through a bank, broker or other financial
institution, either in book-entry form or in street name, you
should check with your own institution to find out:
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how it handles securities
payments and notices; |
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whether it imposes fees or
charges; |
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how it would handle a request for
the holders’ consents, if ever required; |
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whether and how you can instruct
it to send you securities registered in your own name so you can be
a registered holder, if that is permitted in the
future; |
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how it would exercise rights
under the securities if there were a default or other event
triggering the need for holders to act to protect their interests;
and |
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if the securities are in
book-entry form, how the depositary’s rules and procedures will
affect these matters. |
Global Securities
A global security is a security that represents one or any other
number of individual securities held by a depositary. Generally,
all securities represented by the same global securities will have
the same terms.
Each security issued in book-entry form will be represented by a
global security that we deposit with and register in the name of a
financial institution or its nominee that we select. The financial
institution that we select for this purpose is called the
depositary. Unless we specify otherwise in the applicable
prospectus supplement, The Depository Trust Company, New York, New
York, known as DTC, will be the depositary for all securities
issued in book-entry form.
A global security may not be transferred to or registered in the
name of anyone other than the depositary, its nominee or a
successor depositary, unless special termination situations arise.
We describe those situations below under the section titled
“Special Situations When a Global Security Will Be Terminated” in
this prospectus. As a result of these arrangements, the depositary,
or its nominee, will be the sole registered owner and holder of all
securities represented by a global security, and investors will be
permitted to own only beneficial interests in a global security.
Beneficial interests must be held by means of an account with a
broker, bank or other financial institution that in turn has an
account with the depositary or with another institution that does.
Thus, an investor whose security is represented by a global
security will not be a holder of the security, but only an indirect
holder of a beneficial interest in the global security.
If the prospectus supplement for a particular security indicates
that the security will be issued in global form only, then the
security will be represented by a global security at all times
unless and until the global security is terminated. If termination
occurs, we may issue the securities through another book-entry
clearing system or decide that the securities may no longer be held
through any book-entry clearing system.
Special Considerations for Global Securities
The rights of an indirect holder relating to a global security will
be governed by the account rules of the investor’s financial
institution and of the depositary, as well as general laws relating
to securities transfers. We do not recognize an indirect holder as
a holder of securities and instead deal only with the depositary
that holds the global security.
If securities are issued only in the form of a global security, an
investor should be aware of the following:
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an investor cannot cause the
securities to be registered in his or her name, and cannot obtain
non-global certificates for his or her interest in the securities,
except in the special situations we describe below; |
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an investor will be an indirect
holder and must look to his or her own bank or broker for payments
on the securities and protection of his or her legal rights
relating to the securities, as we describe above; |
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an investor may not be able to
sell interests in the securities to some insurance companies and to
other institutions that are required by law to own their securities
in non-book-entry form; |
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an investor may not be able to
pledge his or her interest in a global security in circumstances
where certificates representing the securities must be delivered to
the lender or other beneficiary of the pledge in order for the
pledge to be effective; |
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the depositary’s policies, which
may change from time to time, will govern payments, transfers,
exchanges and other matters relating to an investor’s interest in a
global security. We and any applicable trustee have no
responsibility for any aspect of the depositary’s actions or for
its records of ownership interests in a global security. We and the
trustee also do not supervise the depositary in any
way; |
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the depositary may, and we
understand that DTC will, require that those who purchase and sell
interests in a global security within its book-entry system use
immediately available funds, and your broker or bank may require
you to do so as well; and |
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financial institutions that
participate in the depositary’s book-entry system, and through
which an investor holds its interest in a global security, may also
have their own policies affecting payments, notices and other
matters relating to the securities |
There may be more than one financial intermediary in the chain of
ownership for an investor. We do not monitor and are not
responsible for the actions of any of those intermediaries.
Special Situations When a Global Security Will Be
Terminated
In a few special situations described below, the global security
will terminate and interests in it will be exchanged for physical
certificates representing those interests. After that exchange, the
choice of whether to hold securities directly or in street name
will be up to the investor. Investors must consult their own banks
or brokers to find out how to have their interests in securities
transferred to their own name, so that they will be direct holders.
We have described the rights of the holders and street name
investors above.
Unless we provide otherwise in the applicable prospectus
supplement, the global security will terminate when the following
special situations occur:
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if the depositary notifies us
that it is unwilling, unable or no longer qualified to continue as
depositary for that global security and we do not appoint another
institution to act as depositary within 90 days; |
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• |
if we notify any applicable
trustee that we wish to terminate that global security;
or |
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• |
if an event of default has
occurred with regard to securities represented by that global
security and has not been cured or waived. |
The applicable prospectus supplement may also list additional
situations for terminating a global security that would apply only
to the particular series of securities covered by the applicable
prospectus supplement. When a global security terminates, the
depositary, and not we or any applicable trustee, is responsible
for deciding the names of the institutions that will be the initial
direct holders.
PLAN OF
DISTRIBUTION
We may sell the securities covered by this prospectus from time to
time in one or more offerings. Registration of the securities
covered by this prospectus does not mean, however, that those
securities will necessarily be offered or sold.
We may sell our securities, separately or together, in any one or
more of the following ways:
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• |
directly to investors, including
through a specific bidding, auction or other process; |
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• |
to investors through
agents; |
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• |
to or through brokers or
dealers; |
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• |
to the public through
underwriting syndicates led by one or more managing
underwriters; |
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• |
in “at the market” offerings,
within the meaning of Rule 415(a)(4) of the Securities Act or
through a market maker or into an existing trading market on an
exchange or otherwise; |
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• |
to one or more underwriters
acting alone for resale to investors or to the public;
and |
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• |
through any combination of the
foregoing. |
Sales of securities may be effected from time to time in one or
more transactions, including negotiated transactions:
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• |
at a fixed price or prices, which
may be changed; |
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• |
at market prices prevailing at
the time of sale; |
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• |
at prices related to prevailing
market prices; or |
We will describe the method of distribution of the securities and
the terms of the offering in the prospectus supplement. Any
discounts or concessions allowed or re-allowed or paid to dealers
may be changed from time to time.
If underwriters are used in the sale of any securities, the
securities will be acquired by the underwriters for their own
account and may be resold from time to time in one or more
transactions described above. The securities may be either offered
to the public through underwriting syndicates represented by
managing underwriters, or directly by underwriters. Generally, the
underwriters’ obligations to purchase the securities will be
subject to conditions precedent and the underwriters will be
obligated to purchase all of the securities if they purchase any of
the securities. We may use underwriters with whom we have a
material relationship. We will describe in the prospectus
supplement, naming the underwriter, the nature of any such
relationship.
We may authorize underwriters, dealers or agents to solicit offers
by certain purchasers to purchase the securities from us at the
public offering price set forth in the prospectus supplement
pursuant to delayed delivery contracts providing for payment and
delivery on a specified date in the future. The contracts will be
subject only to those conditions set forth in the prospectus
supplement, and the prospectus supplement will set forth any
commissions we pay for solicitation of these contracts.
We may enter into derivative transactions with third parties, or
sell securities not covered by this prospectus to third parties in
privately negotiated transactions. If the applicable prospectus
supplement indicates, in connection with those derivative
transactions, the third parties may sell securities covered by this
prospectus and the applicable prospectus supplement, including in
short sale transactions. If so, the third party may use securities
pledged by us or borrowed from us or others to settle those sales
or to close out any related open borrowings of stock, and may use
securities received from us in settlement of those derivatives to
close out any related open borrowings of stock. The third party in
such sale transactions will be an underwriter and will be
identified in the applicable prospectus supplement or in a
post-effective amendment.
Underwriters, dealers and agents may be entitled to indemnification
by us against certain civil liabilities, including liabilities
under the Securities Act, or to contribution with respect to
payments made by the underwriters, dealers or agents, under
agreements between us and the underwriters, dealers and agents.
We may grant underwriters who participate in the distribution of
securities an option to purchase additional securities to cover
over-allotments, if any, in connection with the distribution.
Underwriters, dealers or agents may receive compensation in the
form of discounts, concessions or commissions from us or our
purchasers, as their agents in connection with the sale of
securities. These underwriters, dealers or agents may be considered
to be underwriters under the Securities Act. As a result,
discounts, commissions or profits on resale received by the
underwriters, dealers or agents may be treated as underwriting
discounts and commissions. The prospectus supplement will identify
any such underwriter, dealer or agent and describe any compensation
received by them from us. Any initial public offering price and any
discounts or concessions allowed or re-allowed or paid to dealers
may be changed from time to time.
Unless otherwise specified in the related prospectus supplement,
all securities we offer, other than common stock, will be new
issues of securities with no established trading market. Any
underwriters may make a market in these securities, but will not be
obligated to do so and may discontinue any market making at any
time without notice. Any common stock sold pursuant to a prospectus
supplement will be listed on the Nasdaq Capital Market or other
principal market for our common stock. We may apply to list any
series of preferred stock or warrants on an exchange, but we are
not obligated to do so. Therefore, there may not be liquidity or a
trading market for any such series of preferred stock or such
warrants.
Any underwriter may engage in over-allotment transactions,
stabilizing transactions, short-covering transactions and penalty
bids in accordance with Regulation M under the Exchange Act.
Over-allotment involves sales in excess of the offering size, which
create a short position. Stabilizing transactions permit bids to
purchase the underlying security so long as the stabilizing bids do
not exceed a specified maximum. Short covering transactions involve
purchases of the securities in the open market after the
distribution is completed to cover short positions. Penalty bids
permit the underwriters to reclaim a selling concession from a
dealer when the securities originally sold by the dealer are
purchased in a covering transaction to cover short positions. Those
activities may cause the price of the securities to be higher than
it would otherwise be. If commenced, the underwriters may
discontinue any of the activities at any time. We make no
representation or prediction as to the direction or magnitude of
any effect that such transactions may have on the price of the
securities. For a description of these activities, see the
information under the section titled “Underwriting” or “Plan of
Distribution” in the applicable prospectus supplement.
Underwriters, broker-dealers or agents who may become involved in
the sale of the common stock may engage in transactions with and
perform other services for us in the ordinary course of their
business for which they receive compensation.
LEGAL MATTERS
The validity of the issuance of the securities offered hereby will
be passed upon for us by Winstead PC, Houston, Texas. The validity
of any securities will be passed upon for any underwriters or
agents by counsel that we will name in the applicable prospectus
supplement.
EXPERTS
The consolidated financial statements as of December 31, 2018 and
2017 and for the years then ended incorporated by reference in this
prospectus have been so incorporated in reliance on the report of
BDO USA, LLP, an independent registered public accounting firm,
incorporated herein by reference, given on the authority of said
firm as experts in auditing and accounting.
WHERE YOU CAN FIND MORE
INFORMATION
We file annual, quarterly and current reports, proxy statements and
other information with the SEC. The SEC maintains an Internet site
that contains reports, proxy and information statements, and other
information regarding issuers that file electronically with the
SEC, including us. The SEC’s Internet site can be found
at http://www.sec.gov. In addition, we make available
on or through our Internet site copies of these reports as soon as
reasonably practicable after we electronically file or furnished
them to the SEC. Our Internet site can be found
at http://www.biopathholdings.com. The information
contained in, or that can be accessed through, our website is not
incorporated by reference in, and is not part of, this
prospectus.
INFORMATION INCORPORATED BY
REFERENCE
We are incorporating by reference into this prospectus certain
information that we file with the SEC, which means that we are
disclosing important information to you by referring you to those
documents. The information incorporated by reference is deemed to
be part of this prospectus, except for information incorporated by
reference that is superseded by information contained in this
prospectus. This means that you must look at all of the SEC filings
that we incorporate by reference to determine if any statements in
the prospectus or any document previously incorporated by reference
have been modified or superseded. This prospectus incorporates by
reference the documents set forth below that we have previously
filed with the SEC:
|
• |
the description of our common
stock contained in our registration statement on Form 8-A filed
with the SEC on
March 5, 2014, as updated by our Current Report on Form 8-K
filed with the SEC on
January 6, 2015. |
Any information in any of the foregoing documents will
automatically be deemed to be modified or superseded to the extent
that information in this prospectus or in a later filed document
that is incorporated or deemed to be incorporated herein by
reference modifies or replaces such information.
We also incorporate by reference all documents we file in the
future pursuant to Section 13(a), 13(c), 14 or 15(d) of the
Exchange Act (i) after the date of the filing of the registration
statement of which this prospectus is a part and prior to the
effectiveness of such registration statement or (ii) after the date
of this prospectus and until the offering of the securities made by
this prospectus is terminated. These documents include periodic
reports, such as Annual Reports on Form 10-K, Quarterly Reports on
Form 10-Q and Current Reports on Form 8-K (except, in any such
case, the portions furnished and not filed pursuant to Item 2.02,
Item 7.01 or otherwise), as well as any proxy statements.
We will provide to each person, including any beneficial owner, to
whom a prospectus is delivered, without charge upon written or oral
request, a copy of any or all of the documents that are
incorporated by reference into this prospectus but not delivered
with the prospectus, including exhibits which are specifically
incorporated by reference into such documents. You may request a
copy of these filings at no cost, by writing to or telephoning us
at the following address:
Bio-Path Holdings, Inc.
Attention: Secretary
4710 Bellaire Boulevard, Suite 210
Bellaire, Texas 77401
(832) 742-1357
1,710,600 SHARES OF COMMON STOCK
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February 16, 2021