Gelteq Receives FDA Approval of its Suitability Petition for New Animal Drug
17 Dezembro 2024 - 10:30AM
Gelteq Limited (NASDAQ: GELS) (“Gelteq” or the “Company”), a
clinical and biotechnology company focused on developing and
commercializing white label gel-based delivery solutions for
prescription drugs, nutraceuticals, pet care, sports, and other
products, announces today that the U.S. Food and Drug
Administration (“FDA”) has approved its suitability petition for a
new animal drug under development. The new animal drug leverages
Gelteq’s ingestible gel platform designed for nutrient and drug
delivery. A suitability petition is a request by a drug sponsor to
submit an abbreviated new animal drug application (“ANADA”) for a
proposed innovative new animal drug that differs from a previously
FDA approved generic animal drug.
“We believe there is enormous opportunity for us in
the animal pharmaceuticals market, as there is a significant need
to deliver medications more efficiently,” Gelteq co-founder and CEO
Nathan Givoni said. “This pathway, which is essentially a faster
track as opposed to the standard new animal drug application (NADA)
pathway, is a strategic way for us to expedite our entry into the
animal drug space and provide long-term value for all our
stakeholders.”
Gelteq has proposed changing the reference drug
from a pill form into an oral gel form. These changes could be
considered through the suitability petition, as defined under
section 512(n)(3) of the Federal Food, Drug, and Cosmetic Act (the
“FD&C Act”). The FDA found that the proposed changes did not
require Gelteq to conduct further investigations to show the safety
and effectiveness of the innovative new animal drug for its
intended uses. Therefore, the FDA approved the petition under
section 512(n)(3)(C) of the FD&C Act which foregoes the safety
and effectiveness studies and helps reduce the timeframe to reach
potential approval of the new animal drug. This approval of
the suitability petition, however, does not guarantee approval of
the ANADA for Gelteq’s proposed generic new animal drug.
About Gelteq Limited:Headquartered in
Melbourne, Australia, Gelteq (NASDAQ: GELS) is a clinical and
biotechnology company that is focused on developing and
commercializing white label gel-based delivery solutions for
prescription drugs, nutraceuticals, pet care and other products.
Gelteq is focused on advancing and commercializing its delivery
solutions within five core verticals: pharmaceuticals,
over-the-counter medications, nutraceuticals, animal medications,
and sports nutrition. Gelteq’s unique formulation directly
addresses the issues associated with traditional drug delivery
methods such as difficulty swallowing, taste of unpalatable
ingredients, and dosage control. For more information,
visit www.gelteq.com.
Forward-Looking Statements Certain
statements in this press release may constitute “forward-looking
statements” within the meaning of the Private Securities Litigation
Reform Act of 1995. All statements, other than statements of
historical fact, contained in this press release are
forward-looking statements. Forward-looking statements contained in
this press release may be identified by the use of words such as
“anticipate,” “believe,” “contemplate,” “could,” “estimate,”
“expect,” “intend,” “seek,” “may,” “might,” “plan,” “potential,”
“predict,” “project,” “suggest,” “target,” “aim,” “should,” "will,”
“would,” or the negative of these words or other similar
expressions, although not all forward-looking statements contain
these words. Forward-looking statements are based on Gelteq’s
current expectations and are subject to inherent uncertainties,
risks and assumptions that are difficult to predict, including
risks related to the timing and fulfilment of current and future
orders relating to Gelteq’s products, the success of new programs,
the ability to implement a new strategic plan and the success of a
new strategic plan. Further, certain forward-looking statements are
based on assumptions as to future events that may not prove to be
accurate. For a further discussion of risks and uncertainties that
could cause actual results to differ from those expressed in these
forward-looking statements, as well as risks relating to the
business of Gelteq in general, see the risk factors in the Annual
Report on 20-F filed on November 15, 2024. All such
forward-looking statements speak only as of the date they are made,
and Gelteq undertakes no obligation to update or revise these
statements, whether as a result of new information, future events
or otherwise.
Contact: CORE
IR516-222-2560pr@gelteq.com
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