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UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
WASHINGTON, DC 20549
FORM 8-K
CURRENT REPORT
Pursuant to Section 13 or 15(d) of the
Securities Exchange Act of 1934
Date of report (Date of earliest event reported):
December 27, 2023
|
First Wave BioPharma, Inc. |
|
|
(Exact name of registrant as specified in its charter) |
|
Delaware |
|
001-37853 |
|
46-4993860 |
(State or other jurisdiction of incorporation) |
|
(Commission File Number) |
|
(IRS Employer Identification No.) |
777 Yamato Road, Suite 502
Boca Raton, Florida |
|
33431 |
(Address of principal executive offices) |
|
(Zip Code) |
Registrant’s telephone number, including
area code: (561) 589-7020
Not Applicable
(Former name or former address, if changed since
last report)
Check the appropriate box below if the Form 8-K
filing is intended to simultaneously satisfy the filing obligation of the registrant under any of the following provisions:
¨ |
Written communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425) |
¨ |
Soliciting material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12) |
¨ |
Pre-commencement communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b)) |
¨ |
Pre-commencement communications pursuant to Rule 13e-4(c) under the Exchange Act (17 CFR 240.13e-4(c)) |
Securities registered pursuant to Section 12(b)
of the Act:
Title of each class |
|
Trading Symbol(s) |
|
Name of each exchange on which
registered |
Common Stock, par value $0.0001 per share |
|
FWBI |
|
Nasdaq Capital Market |
Indicate by check mark whether the registrant is an emerging growth company as defined in Rule 405 of the Securities Act of 1933 (§230.405
of this chapter) or Rule 12b-2 of the Securities Exchange Act of 1934 (§240.12b-2 of this chapter).
Emerging growth company ¨
If an emerging growth company, indicate by check
mark if the registrant has elected not to use the extended transition period for complying with any new or revised financial accounting
standards provided pursuant to Section 13(a) of the Exchange Act. ¨
On
December 27, 2023, First Wave BioPharma, Inc. (the “Company”) announced it has entered into a non-binding letter of
intent (the “Niclosamide LOI”) for the sale of the Company’s niclosamide program, which is designed to treat
inflammatory bowel diseases such as ulcerative colitis and related conditions, to an undisclosed biopharmaceutical company (the
“Niclosamide Sale”). The Niclosamide LOI contemplates a low seven-figure upfront payment to the Company for the rights
to Niclosamide, as well as economics to the Company related to future milestones and royalties.
The Niclosamide LOI only
represents a mutual indication of interest regarding the Niclosamide Sale and the terms of the Niclosamide Sale are subject to a number
of contingencies, including the completion of customary due diligence and the negotiation and execution of definitive agreements. Upon
execution of the definitive agreement, the completion of the transaction will be subject to, among other matters, satisfaction of the
conditions negotiated therein, the buyer having secured adequate financing, and receipt of all third party (including governmental) approvals,
licenses, consents, and clearances, as and when applicable. There can be no assurance that the Niclosamide Sale will be completed on the
terms contemplated in the Niclosamide LOI or otherwise. In particular, the timing of closing of any such transaction and the aggregate
consideration that we may receive may materially differ from that currently contemplated by the Niclosamide LOI.
A
copy of the press release is attached as Exhibit 99.1 to this Current Report on Form 8-K and incorporated herein by reference.
Item 9.01 |
Financial Statements and Exhibits. |
(d) Exhibits
The
following exhibits are being filed or furnished, as applicable, with this Current Report on Form 8-K:
SIGNATURES
Pursuant to the requirements of the Securities
Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned hereunto duly authorized.
|
First Wave BioPharma, Inc. |
|
|
December 27, 2023 |
By: |
/s/ James Sapirstein |
|
Name: |
James Sapirstein |
|
Title: |
Chief Executive Officer |
Exhibit 99.1
First Wave BioPharma
Announces Streamlining of Clinical Pipeline with Non-Binding Term Sheet to Sell Niclosamide IBD Program
First Wave BioPharma
to advance GI development pipeline with the expected addition of Phase 3 Latiglutenase celiac disease program and Phase 2 clinical programs
built around Capeserod and Adrulipase
BOCA RATON, FL, December
27, 2023 – First Wave BioPharma, Inc., (NASDAQ: FWBI), (“First Wave BioPharma” or the “Company”), a
clinical-stage biopharmaceutical company specializing in the development of targeted, non-systemic therapies for gastrointestinal
(GI) diseases, today announced that it has entered a non-binding term sheet to sell its Niclosamide program for the treatment of inflammatory
bowel diseases (IBD) such as ulcerative colitis and related conditions to an undisclosed biopharmaceutical company (the “Proposed
Transaction”). The Proposed Transaction will enable First Wave BioPharma to focus its development resources on its three late-stage
clinical programs: Capeserod, a selective 5-HT4 receptor partial agonist licensed from Sanofi; Adrulipase, a recombinant lipase enzyme
for the treatment of exocrine pancreatic insufficiency (EPI); and, after the closing of the recently announced potential business combination
with ImmunogenX, Latiglutenase, a Phase 3-ready oral biotherapeutic for celiac disease.
The non-binding term sheet includes a low
seven-figure upfront payment to First Wave BioPharma for rights to Niclosamide, as well as economics related to future milestones and
royalties. The transaction is expected to close in the first half of 2024. Additional details of the transaction will be disclosed upon
finalization and execution of the definitive agreement. Upon execution of the definitive agreement, the completion of the transaction
will be subject to, among other matters, satisfaction of the conditions negotiated therein, the buyer having secured adequate financing,
and receipt of all third party (including governmental) approvals, licenses, consents, and clearances, as and when applicable.
“This is a very
exciting time in the evolution of First Wave BioPharma as we have recently reinvigorated our GI-focused clinical development pipeline
with Phase 2-ready Capeserod from Sanofi and the pending addition of Phase 3-ready Latiglutenase,” stated James Sapirstein, President
and CEO of First Wave BioPharma. “We plan to rapidly advance these programs in 2024 given the significant potential of each to address
GI conditions for which no effective therapies currently exist. As a result, we made the strategic decision to streamline our development
pipeline and are pleased to have entered a non-binding term sheet for Niclosamide, which has the potential to infuse First Wave with additional,
non-dilutive capital.”
Niclosamide is a prescription,
non-systemic, small molecule drug listed as an essential medicine by the World Health Organization (WHO). Niclosamide was approved by
the U.S. Food and Drug Administration (FDA) in 1982 for the treatment of intestinal tapeworm infections and has been safely used on millions
of patients. The drug is a potential non-steroidal anti-inflammatory therapy for the treatment of mild-to-moderate inflammatory bowel
diseases (IBD). First Wave BioPharma had previously conducted Phase 2 trials with niclosamide for the treatment of ulcerative proctitis/proctosigmoiditis
(the most prevalent form of ulcerative colitis) and for the treatment of COVID gastrointestinal infections. The Company also has a Phase
2 open-IND for the treatment of immune checkpoint inhibitor-associated colitis and diarrhea in patients with metastatic cancer. Intellectual
property for niclosamide formulations governing composition of matter and methods of use extends beyond 2040.
About First Wave BioPharma, Inc.
First Wave BioPharma is a clinical-stage biopharmaceutical
company specializing in the development of targeted, non-systemic therapies for gastrointestinal (GI) diseases. The Company is currently
advancing a therapeutic development pipeline with multiple late-stage clinical stage programs, including Capeserod, a selective 5-HT4
receptor partial agonist which First Wave is developing for gastrointestinal (GI) indications; the biologic Adrulipase, a recombinant
lipase enzyme designed to enable the digestion of fats and other nutrients in cystic fibrosis and chronic pancreatitis patients with exocrine
pancreatic insufficiency; and it is anticipated that the Company will soon acquire Latiglutenase, a targeted, oral first-in-class biotherapeutic
for celiac disease. First Wave BioPharma is headquartered in Boca Raton, Florida. For more information visit www.firstwavebio.com.
Forward-Looking Statements
This press release may contain certain statements
relating to future results which are forward-looking statements. It is possible that the Company’s actual results and financial
condition may differ, possibly materially, from the anticipated results and financial condition indicated in these forward-looking statements,
depending on factors including whether a definitive agreement for the Proposed Transaction or a transaction with ImmunogenX and any concurrent
financing or licensing transaction will be entered into; whether such transactions, or any other contemplated transaction, may be completed
with different terms, in an untimely manner, or not at all; whether the Company will be able to realize the benefits of the Proposed
Transaction described herein; the Company’s ability to integrate the assets and commercial operations contemplated to be acquired
from ImmunogenX into the Company’s business; whether results obtained in preclinical and nonclinical studies and clinical trials
will be indicative of results obtained in future clinical trials; whether preliminary or interim results from a clinical trial will be
indicative of the final results of the trial; whether the Company will be able to maintain compliance with Nasdaq’s continued listing
criteria and the effect of a delisting from Nasdaq on the market for the Company’s securities; the size of the potential markets
for the Company’s drug candidates and its ability to service those markets; the effects of the First Wave Bio, Inc. acquisition,
the related settlement and their effect on the Company’s business, operating results and financial prospects; and the Company’s
current and future capital requirements and its ability to raise additional funds to satisfy its capital needs. Additional information
concerning the Company and its business, including a discussion of factors that could materially affect the Company’s financial
results are contained in the Company’s Annual Report on Form 10-K for the year ended December 31, 2022, under the heading “Risk
Factors,” as well as the Company’s subsequent filings with the Securities and Exchange Commission. All forward-looking statements
included in this press release are made only as of the date of this press release, and we do not undertake any obligation to publicly
update or correct any forward-looking statements to reflect events or circumstances that subsequently occur or of which we hereafter
become aware.
For more information:
First Wave BioPharma, Inc.
777 Yamato Road, Suite 502
Boca Raton, FL 33431
Phone: (561) 589-7020
info@firstwavebio.com
Media contact:
Tiberend Strategic Advisors, Inc.
David Schemelia
(609) 468-9325
dschemelia@tiberend.com
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