Vallon Pharmaceuticals Announces Issuance of New European Patent Covering Method of Use and Composition of Matter for ADAIR
July 13 2021 - 8:05AM
Vallon Pharmaceuticals Inc. (NASDAQ: VLON), (“Vallon” or the
“Company”), a clinical-stage biopharmaceutical company primarily
focused on the development of novel drugs that are designed to
deter abuse in the treatment of central nervous system (CNS)
disorders, today announced that the European Patent Office has
issued patent number EP3576719B1 covering ADAIR1, the Company’s
proprietary abuse-deterrent formulation of immediate-release
dextroamphetamine.
ADAIR is being developed for Europe and the UK
through a license and collaboration agreement with MEDICE
Arzneimittel Pütter GmbH, a leader in the European ADHD market.
Under the terms of the agreement, Vallon will receive development
and sales milestone payments and double-digit sales-based royalty
payments. The issuance of this Composition of Matter and Method of
Use patent provides additional protection as MEDICE works towards
the potential commercialization of ADAIR in the European Union and
United Kingdom. In the US, the Company continues to develop ADAIR,
leveraging the 505(b)(2) regulatory pathway. The Company is
currently conducting a pivotal intranasal abuse study, the SEAL
Study, in recreational drug abusers.
David Baker, President & Chief Executive
Officer of Vallon commented, “There is a clear and growing unmet
need for products that can treat ADHD effectively while attending
to the significant problem of stimulant misuse. We continue to be
encouraged by the potential of our novel platform technology, which
we believe can also be applied to other prescription drugs that
have abuse potential. We are pleased to successfully expand our
intellectual property portfolio with the issuance of this new
European patent.”
The new European patent covers composition of
matter and method of use for ADAIR, with a base patent term
extending until 2038. The design and development of an
abuse-deterrent formulation involves the balance of limiting the
potential for manipulation and abuse while maintaining acceptable
dissolution rates and bioavailability. ADAIR was previously granted
two patents in the United States with a base patent term extending
until 2037, excluding patent term extensions.
About ADAIR
ADAIR (Abuse Deterrent Amphetamine Immediate
Release) is an investigational new drug; a novel, patented
formulation of dextroamphetamine designed to deter attempts to
crush and snort it or take it by other non-oral routes that can
produce a greater “high.” Dextroamphetamine has been used
clinically for more than 50 years. It is the same active ingredient
used in FDA-approved products, such as Adderall®, Dexedrine®, and
Vyvanse®. ADAIR is not approved by the FDA.
About Vallon
Pharmaceuticals Inc.
Vallon Pharmaceuticals Inc. is a clinical-stage
biopharmaceutical company, headquartered in Philadelphia, PA. The
Company is focused on the development of new medications to help
patients with central nervous system (CNS) disorders. The Company’s
lead investigational product candidate, ADAIR, is a novel abuse
deterrent formulation of amphetamine immediate release being
developed for the treatment of ADHD and narcolepsy.
For more information about the company, please
visit www.vallon-pharma.com or connect with us on LinkedIn or
Twitter.
References and links to websites have been
provided for convenience, and the information contained on any such
website is not a part of, or incorporated by reference into, this
press release. Vallon is not responsible for the contents of
third-party websites.
Forward Looking Statements
This press release contains “forward-looking
statements” that are based on Vallon’s current expectations and
subject to inherent uncertainties, risks and assumptions that are
difficult to predict, including, without limitation, Vallon’s
ability to execute its business plan, continue its growth and fund
its ongoing business activities as planned, Vallon’s ability to
develop and commercialize its product candidates, expectations
related to results of clinical trials and studies, Vallon’s
expectations with respect to the important advantages it believes
its abuse-deterrent formulation of drugs have over similar drugs in
the market and the growing need for abuse-deterrent formulations of
drugs, Vallon’s ability to utilize the 505(b)(2) regulatory
pathway, Vallon’s ability to obtain FDA approval of ADAIR and its
other product candidates, and Vallon’s expectations with respect to
its cash runway. Forward-looking statements may be identified by
the use of words such as “anticipate,” “believe,” “contemplate,”
“could,” “estimate,” “expect,” “intend,” “seek,” “may,” “might,”
“plan,” “potential,” “predict,” “project,” “target,” “aim,”
“should,” "will,” “would,” or the negative of these words or other
similar expressions. Further, certain forward-looking statements
are based on assumptions as to future events that may not prove to
be accurate. These and other risks and uncertainties are described
more fully in the section titled “Risk Factors” in Vallon’s
Quarterly and Annual Reports filed with the U.S. Securities and
Exchange Commission. Forward-looking statements contained in this
announcement are made as of this date, and the Company undertakes
no duty to update such information except as required under
applicable law.
Investor Contact:
JTC Team, LLCJenene Thomas(833) 475-8247vallon@jtcir.com
1 ADAIR is not approved by the FDA
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