Adial Pharmaceuticals Signs Agreement with Boudicca Dx to Advance Regulatory Strategy for Companion Diagnostic Genetic Test for AD04
13 August 2024 - 3:00PM
Adial Pharmaceuticals, Inc. (
NASDAQ: ADIL)
(“Adial” or the “Company”), a clinical-stage biopharmaceutical
company focused on developing therapies for the treatment and
prevention of addiction and related disorders, announced a
collaboration with Boudicca Dx, LLC, a global precision medicine
testing accelerator.
Under the agreement, Boudicca will support Adial
in advancing its technical and regulatory strategy for the
Company’s companion diagnostic genetic test, to ensure it is
validated both technically and clinically per FDA guidelines as
part of Adial’s regulatory strategy for its lead investigational
asset, AD04, a genetically targeted, serotonin-3 receptor
antagonist, therapeutic agent for the treatment of Alcohol Use
Disorder (AUD). Adial’s companion diagnostic is intended to
accompany AD04 in identifying potential patients, including
recruitment for the Company’s planned Phase 3 program.
Cary Claiborne, President and Chief Executive
Officer of Adial commented, “As we continue to prepare for the
Phase 3 study for AD04, this agreement with Boudicca Dx is another
key component toward achieving clinical success and is expected to
support our next FDA interaction. Kelly Gordon, the Chief Executive
Officer and founder of Boudicca Dx, along with her team, are the
ideal partners for Adial to develop a comprehensive clinical,
regulatory and commercial strategy for the AD04 companion
diagnostic. Our mission is to bring a first in class precision
medicine to the treatment of AUD, and having our companion
diagnostic validated by the FDA is a critical step in the
process.”
Kelly Gordon commented, “The Boudicca Dx team is
excited to support the development of a first-in-class companion
diagnostic test for AD04, a precision medicine designed to treat
patients with Alcohol Use Disorder. This disease affects more than
30 million people in the US alone and causes 3 million deaths
worldwide each year. There is a high unmet need for a targeted
therapy and its companion diagnostic test.”
About Adial Pharmaceuticals, Inc.
Adial Pharmaceuticals is a clinical-stage biopharmaceutical
company focused on the development of treatments for addictions and
related disorders. The Company’s lead investigational new drug
product, AD04, is a genetically targeted, serotonin-3 receptor
antagonist, therapeutic agent for the treatment of Alcohol Use
Disorder (AUD) in heavy drinking patients and was recently
investigated in the Company’s ONWARD™ pivotal Phase 3 clinical
trial for the potential treatment of AUD in subjects with certain
target genotypes identified using the Company’s companion
diagnostic genetic test. ONWARD showed promising results in
reducing drinking in heavy drinking patients, and no overt safety
or tolerability concerns. AD04 is also believed to have the
potential to treat other addictive disorders such as Opioid Use
Disorder, gambling, and obesity. Additional information is
available at www.adial.com.
Forward-Looking Statements
This communication contains certain “forward-looking statements”
within the meaning of the U.S. federal securities laws. Such
statements are based upon various facts and derived utilizing
numerous important assumptions and are subject to known and unknown
risks, uncertainties and other factors that may cause actual
results, performance or achievements to be materially different
from any future results, performance or achievements expressed or
implied by such forward-looking statements. Statements preceded by,
followed by or that otherwise include the words “believes,”
“expects,” “anticipates,” “intends,” “projects,” “estimates,”
“plans” and similar expressions or future or conditional verbs such
as “will,” “should,” “would,” “may” and “could” are generally
forward-looking in nature and not historical facts, although not
all forward-looking statements include the foregoing. The
forward-looking statements include statements regarding Boudicca
supporting us in advancing our technical and regulatory strategy,
our companion diagnostic accompanying AD04 in identifying potential
patients, including recruitment for our planned Phase 3 program,
continuing to prepare for the Phase 3 study for AD04, the agreement
with Boudicca being another key component toward achieving clinical
success and supporting our next FDA interaction. the potential of
AD04 to treat other addictive disorders such as Opioid Use
Disorder, gambling, and obesity. Any forward-looking statements
included herein reflect our current views, and they involve certain
risks and uncertainties, including, among others, our companion
diagnostic being able to accompany AD04 in identifying potential
patients, including recruitment for our planned Phase 3 program,
our ability to prepare and commence the planned Phase 3 program,
our agreement with Boudicca supporting our next FDA interaction and
clinical success, our ability to pursue our regulatory strategy,
our ability to advance ongoing partnering discussions, our ability
to obtain regulatory approvals for commercialization of product
candidates or to comply with ongoing regulatory requirements, our
ability to develop strategic partnership opportunities and maintain
collaborations, our ability to obtain or maintain the capital or
grants necessary to fund our research and development activities,
our ability to complete clinical trials on time and achieve desired
results and benefits as expected, regulatory limitations relating
to our ability to promote or commercialize our product candidates
for specific indications, acceptance of our product candidates in
the marketplace and the successful development, marketing or sale
of our products, our ability to maintain our license agreements,
the continued maintenance and growth of our patent estate and our
ability to retain our key employees or maintain our Nasdaq listing.
These risks should not be construed as exhaustive and should be
read together with the other cautionary statement included in our
Annual Report on Form 10-K for the year ended December 31, 2023,
subsequent Quarterly Reports on Form 10-Q and current reports on
Form 8-K filed with the Securities and Exchange Commission. Any
forward-looking statement speaks only as of the date on which it
was initially made. We undertake no obligation to publicly update
or revise any forward-looking statement, whether as a result of new
information, future events, changed circumstances or otherwise,
unless required by law.
Contact:
Crescendo Communications, LLC
David Waldman / Alexandra Schilt
Tel: 212-671-1020
Email: adil@crescendo-ir.com
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