Gemphire Therapeutics Inc. (Gemphire) (Nasdaq: GEMP), a
clinical-stage biopharmaceutical company focused on developing
therapies for the treatment of dyslipidemia as well as nonalcoholic
fatty liver disease, and NeuroBo Pharmaceuticals, Inc. (NeuroBo), a
privately-held clinical-stage biotechnology company focused on
novel, disease-modifying therapies for neurodegenerative diseases,
today jointly announced that they have entered into a definitive
agreement whereby NeuroBo will merge with a wholly-owned subsidiary
of Gemphire in an all-stock transaction. Upon completion of the
merger, Gemphire will change its name to NeuroBo Pharmaceuticals,
Inc., and plans to change its ticker symbol on the Nasdaq Capital
Market to “NRBO.” The merged company will focus on the development
of NeuroBo’s clinical-stage drug candidates for the treatment of
neurodegenerative diseases.
NeuroBo is focused on the development of a treatment for
diabetic neuropathic pain (DNP), with its lead drug candidate,
NB-01, in Phase 3 clinical development as a first-line,
disease-modifying therapy. NeuroBo’s second drug candidate, NB-02,
is in development for the treatment of neurodegenerative diseases
associated with the pathological dysfunction of the amyloid-beta
and tau proteins in the human brain, which include Alzheimer’s
disease and tauopathies. NeuroBo believes that leveraging the
therapeutic properties of its natural product-based platform will
drive a paradigm shift in the treatment of DNP and other
neurodegenerative diseases where drug safety combined with efficacy
is a strong unmet need.
NeuroBo licensed NB-01 from Korean pharmaceutical company Dong-A
ST. NB-01 has successfully completed Korean and U.S. Phase 2
proof-of-concept clinical trials, showing that NB-01 provided
significant relief of diabetic neuropathic pain with minimal side
effects, compared to placebo. Phase 3 clinical trials are expected
to begin in the fourth quarter of 2019. NeuroBo acquired NB-02
outright from Dong-A ST.
“We are excited about the opportunities and resources that will
become available to NeuroBo and its therapeutic pipeline as a
result of the merger,” explained John L. Brooks III, president and
chief executive officer, NeuroBo Pharmaceuticals. “As we move
towards developing both NB-01 and NB-02, we believe that having
shares publicly traded on Nasdaq will provide greater opportunity
to advance our therapeutic pipeline and corporate strategy.”
Today, Gemphire also announced that the company has signed an
out-licensing partnership with Beijing SL Pharmaceutical Co. Ltd.
to advance its drug candidate, gemcabene, into the Chinese market.
This partnership is expected to provide an upfront gross payment of
$2.5 million to Gemphire and back end milestone and royalty
payments to the combined company if certain development and
commercialization milestones are met.
“NeuroBo represents an ideal merger partner for us,” stated Dr.
Steve Gullans, president and chief executive officer of Gemphire.
“NeuroBo has a compelling Phase 3 program with NB-01 in diabetic
neuropathic pain and a strong team to advance its pipeline. We
evaluated numerous potential merger partners and recognized that
NeuroBo has a solid base of investors and the potential to deliver
significant value based on its pipeline assets. The NeuroBo merger
complements our partnership with Beijing SL Pharmaceutical Co., and
together, these relationships will enable us to continue to advance
gemcabene toward a Food and Drug Administration (FDA) partial
clinical hold decision and potentially lead to a beneficial outcome
for Gemphire shareholders who will hold contingent value
rights.”
About the Proposed Merger Transaction
On a pro forma basis and based upon the number of shares of
Gemphire common stock to be issued in the merger, the pre-merger
Gemphire shareholders will own approximately 4.06% of the
post-merger combined company and the pre-merger NeuroBo investors
will own approximately 95.94% of the post-merger combined company
on a fully-diluted basis. The actual allocation will be subject to
adjustment based on Gemphire’s net cash balance at the time of the
closing of the merger as well as any additional Series B capital
above the minimum required amount and up to a total of $50 million
that NeuroBo may secure at or before the closing of the merger. The
transaction has been approved by the board of directors of both
companies. The merger is expected to close in the second half of
2019, subject to the approval of the stockholders of each company,
as well as other customary closing conditions.
In addition, Gemphire stockholders of record as of immediately
prior to the effective time of the merger will receive
non-transferable contingent value rights (CVRs) entitling the
holders to receive in the aggregate, after the retention of
$500,000 by the combined company and certain other permitted
deductions, 80% of the net proceeds, if any, received during the
15-year period following the merger from transactions entered into
during the 10-year period following the merger involving the sale
or license of gemcabene.
Ladenburg Thalmann & Co. Inc. is acting as financial advisor
to Gemphire for the transaction and Consilium Partners Inc. is
acting as financial advisor to NeuroBo for the transaction. Mintz,
Levin, Cohn, Ferris, Glovsky and Popeo, P.C. is serving as legal
counsel to NeuroBo. Honigman LLP is serving as legal counsel to
Gemphire.
Management and Organization
Following the merger, John L. Brooks III will be appointed to
serve as the post-merger combined company’s president and chief
executive officer. The board of directors for the post-merger
combined company will be comprised of six directors, one of whom
will be Steve Gullans, Ph.D., Gemphire’s current president and
chief executive officer and member of the Gemphire board of
directors.
Conference Call
Gemphire and NeuroBo will host a conference call at 8:30 a.m. ET
on July 25, 2019 to discuss the proposed merger transaction. The
conference call may be accessed by dialing 877-451-6152 for U.S.
callers and 201-389-0879 for international callers at least five
minutes prior to the start of the call and providing the passcode
13693096. Additionally, the live, listen-only webcast of the
conference call can be accessed by visiting the investors and media
section of the Gemphire website at www.gemphire.com, or the
investors and media section of the NeuroBo website at
www.neurobopharma.com. A webcast replay will be available on the
investors and media sections of the Gemphire website for all
interested parties following the call and will be archived and
available for 90 days.
About NeuroBo Pharmaceuticals
NeuroBo Pharmaceuticals Inc. is focused on novel treatments
for neurodegenerative diseases affecting millions of patients
worldwide. The company’s novel lead candidate NB-01 is a drug
candidate for diabetic neuropathic pain. NB-01 is a natural product
candidate that restores nerve growth factor levels in pre-clinical
models of pain. In Phase 2 clinical trials, NB-01 has shown
efficacy comparable to existing therapies and a superior safety
profile. The Phase 3 program with NB-01 is expected to begin in Q4
of 2019, studying diabetic neuropathic pain patients in the U.S.
and a number of other countries. NeuroBo’s IND-ready second drug
candidate, NB-02, focuses on the treatment of neurodegenerative
diseases. NeuroBo Pharmaceuticals, based in Boston, MA, was
jointly founded by Dr. Roy Freeman, professor of neurology at
Harvard Medical School and renowned expert in neuropathic pain, and
JK BioPharma Solutions, a biotechnology consulting company, to
commercialize natural product-based research into ethical
medicines.
About Gemphire
Gemphire is a clinical-stage biopharmaceutical company that is
committed to helping patients with cardiometabolic disorders,
including dyslipidemia and NASH. The company is focused on
providing new treatment options for cardiometabolic diseases
through its complementary, convenient, cost-effective product
candidate, gemcabene, as an add-on to the standard of care,
especially with statins that will benefit patients, physicians, and
payers. Gemphire’s Phase 2 clinical program is evaluating the
efficacy and safety of gemcabene in hypercholesterolemia,
hypertriglyceridemia and fatty liver disease, including Familial
Hypercholesterolemia (FH), Severe Hypertriglyceridemia (SHTG),
Non-alcoholic Steatohepatitis (NASH)/Non-alcoholic Fatty Liver
Disease (NAFLD) and Atherosclerotic Cardiovascular Disease (ASCVD).
Two Phase 2b trials supporting hypercholesterolemia and one Phase
2b trial in SHTG were recently completed under NCT02722408,
NCT02634151 and NCT02944383, respectively.
Important Additional Information Will be Filed with the
SEC
In connection with the proposed transaction between Gemphire and
NeuroBo, the parties intend to file relevant materials with the
SEC, including a registration statement on Form S-4 that will
contain a combined proxy statement/prospectus/information
statement. INVESTORS AND STOCKHOLDERS OF GEMPHIRE AND NEUROBO ARE
URGED TO READ THESE MATERIALS CAREFULLY AND IN THEIR ENTIRETY WHEN
THEY BECOME AVAILABLE BECAUSE THEY WILL CONTAIN IMPORTANT
INFORMATION ABOUT GEMPHIRE, NEUROBO, THE PROPOSED MERGER AND
RELATED MATTERS. Investors and shareholders will be able to obtain
free copies of the proxy statement/prospectus/information statement
and other documents filed by Gemphire with the SEC (when they
become available) through the website maintained by the SEC at
www.sec.gov. In addition, investors and shareholders will be able
to obtain free copies of the proxy statement/prospectus/information
statement and other documents filed by Gemphire with the SEC by
written request to: Gemphire Therapeutics Inc., 17199 N. Laurel
Park Drive, Suite 401, Livonia, MI, 48152, Attention: Corporate
Secretary. Investors and stockholders are urged to read the proxy
statement/prospectus/information statement and the other relevant
materials when they become available before making any voting or
investment decision with respect to the proposed transaction.
No Offer or Solicitation
This communication shall not constitute an offer to sell, the
solicitation of an offer to sell or an offer to buy or the
solicitation of an offer to buy any securities, nor shall there be
any sale of securities in any jurisdiction in which such offer,
solicitation or sale would be unlawful prior to registration or
qualification under the securities laws of any such jurisdiction.
No offer of securities shall be made except by means of a
prospectus meeting the requirements of Section 10 of the Securities
Act of 1933, as amended.
Participants in the Solicitation
Gemphire, and its directors and executive officers, and NeuroBo,
and its directors and executive officers, may be deemed to be
participants in the solicitation of proxies from the stockholders
of Gemphire in connection with the proposed merger. Information
regarding the special interests of these directors and executive
officers in the proposed merger will be included in the proxy
statement/prospectus/information statement referred to above.
Additional information about Gemphire’s directors and executive
officers is included in Gemphire’s Annual Report on Form 10-K for
the year that ended December 31, 2018, filed with the SEC on March
18, 2019. These documents are available free of charge at the SEC
website (www.sec.gov) and from the Corporate Secretary of Gemphire
at the address above.
Forward Looking Statements
Any statements in this press release that are not statements of
historical fact constitute forward-looking statements within the
meaning of The Private Securities Litigation Reform Act of 1995, as
amended, and Section 21E of the Securities Exchange Act of 1934, as
amended. These statements include, but are not limited to,
statements regarding the proposed merger and other contemplated
transactions (including statements relating to satisfaction of the
conditions to and consummation of the proposed merger, the expected
ownership of the combined company and the ability of the combined
company to raise additional capital to complete its clinical
programs and opportunities relating to or resulting from the
merger), and statements regarding the nature, potential approval
and commercial success of NeuroBo’s clinical programs and pipeline,
the effects of having shares of capital stock traded on the Nasdaq
Capital Market, NeuroBo’s and the post-merger combined company’s
financial resources and cash expenditures, the ability of Gemphire
or the post-merger combined company to advance gemcabene through
the FDA partial clinical hold and Gemphire’s or the post-merger
combined company’s potential receipt of payments pursuant to the
Beijing SL Pharmaceuticals licensing partnership. Forward-looking
statements are usually identified by the use of words such as
“believes,” “anticipates,” “expects,” “intends,” “plans,” “ideal,”
“may,” “potential,” “will,” “could” and similar expressions. Actual
results may differ materially from those indicated by
forward-looking statements as a result of various important factors
and risks. These factors, risks and uncertainties include, but are
not limited to: risks relating to the completion of the merger,
including the need for stockholder approval and the satisfaction of
closing conditions; risks that the conditions to the milestone and
royalty payments pursuant to the licensing partnership with Beijing
SL Pharmaceutical Co. may not be met; risks related to Gemphire’s
ability to correctly estimate and manage its operating expenses and
its expenses associated with the proposed merger pending closing;
the cash balances of the combined company following the closing of
the merger; the ability of Gemphire to remain listed on the Nasdaq
Capital Market; the risk that as a result of adjustments to the
exchange ratio, Gemphire shareholders or NeuroBo stockholders could
own more or less of the combined company than is currently
anticipated; the risk that the conditions to payment under the CVRs
will not be met and that the CVRs may otherwise never deliver any
value to Gemphire stockholders; potential adverse reactions or
changes to business relationships resulting from the announcement
or completion of the proposed merger; the success and timing of
regulatory submissions and pre-clinical and clinical trials;
regulatory requirements or developments; changes to clinical trial
designs and regulatory pathways; changes in capital resource
requirements; and other factors discussed in the "Risk Factors"
section of Gemphire’s most recent annual report, subsequent
quarterly reports and in other filings Gemphire makes with the SEC
from time to time. Risks and uncertainties related to NeuroBo that
may cause actual results to differ materially from those expressed
or implied in any forward-looking statement include, but are not
limited to: NeuroBo’s plans to develop and commercialize its
product candidates; the timing of completion of NeuroBo’s planned
clinical trials; the timing of the availability of data from
NeuroBo’s clinical trials; NeuroBo’s plans to research, develop and
commercialize its current and future product candidates; NeuroBo’s
ability to successfully collaborate with existing collaborators or
enter into new collaborations and to fulfill its obligations under
any such collaboration agreements; the clinical utility, potential
benefits and market acceptance of NeuroBo’s product candidates;
NeuroBo’s commercialization, marketing and manufacturing
capabilities and strategy; NeuroBo’s ability to identify additional
products or product candidates with significant commercial
potential; developments and projections relating to NeuroBo’s
competitors and its industry; the impact of government laws and
regulations; NeuroBo’s ability to protect its intellectual property
position; and NeuroBo’s estimates regarding future revenue,
expenses, capital requirements and need for additional financing
following the proposed transaction. In addition, the
forward-looking statements included in this press release represent
Gemphire’s and NeuroBo’s views as of the date hereof. Gemphire and
NeuroBo anticipate that subsequent events and developments will
cause their respective views to change. However, while Gemphire and
NeuroBo may elect to update these forward-looking statements at
some point in the future, Gemphire and NeuroBo specifically
disclaim any obligation to do so. These forward-looking statements
should not be relied upon as representing Gemphire’s or NeuroBo’s
views as of any date subsequent to the date hereof.
Gemphire Contact:
Ashley RobinsonLifeSci Advisors LLC(617) 535-7742
NeuroBo Contact:
Nicole FranklinRacepoint Global(617)
624-3264nfranklin@racepointglobal.com
Gemphire Therapeutics (NASDAQ:GEMP)
Gráfico Histórico do Ativo
De Dez 2024 até Jan 2025
Gemphire Therapeutics (NASDAQ:GEMP)
Gráfico Histórico do Ativo
De Jan 2024 até Jan 2025