Enveric Biosciences Announces Preclinical Results Confirming Potential of EB-003 to be Dosed Orally
25 Julho 2024 - 9:00AM
Business Wire
Confirmation of oral bioavailability and
significant brain exposure in rodent models supports expedited
development of EB-003, with Investigational New Drug (IND) filing
and first patient dosed expected in 2025
Enveric Biosciences (NASDAQ: ENVB) (“Enveric”), a biotechnology
company dedicated to the development of novel neuroplastogens for
the treatment of neuropsychiatric disorders, today announced
encouraging EB-003 preclinical results indicating the potential for
the drug candidate to be delivered via oral administration with
significant brain exposure in rodent models at potential
therapeutic doses. EB-003 is a novel, neuroplastogenic molecule
designed to treat severe mental health disorders without the
hallucinogenic effect typically associated with DMT
(N,N-Dimethyltryptamine) and other psychedelic compounds.
EB-003 exhibited good oral bioavailability and brain penetration
in a mouse pharmacokinetic study, with a brain:plasma exposure
ratio of ~1.5. Furthermore EB-003 demonstrated significant in vitro
stability against human monoamine oxidase-A (MAO-A) as well as in
mouse, rat, dog, and human liver microsomes. By contrast, DMT and
similar analogs are not orally available due to rapid metabolism by
MAO-A.
Based on these results, Enveric is accelerating its evaluation
of EB-003 in several in vivo animal efficacy models to determine
the optimal therapeutic indication for clinical development and
expected dose range. Enveric now expects to file an IND application
for EB-003 by the third quarter of 2025 and initiate clinical
development by the end of 2025.
“We continue to believe that EB-003 is substantially
differentiated from the various psychedelic-inspired compounds in
development. Not only does EB-003 offer the potential to
significantly reduce or eliminate the hallucinogenic side-effect
common to DMT and related analogs, but we now have confirmation
that EB-003 can potentially be administered orally and penetrate
the brain at levels expected to elicit the desired therapeutic
effect,” said Joseph Tucker, Ph.D., CEO of Enveric. “We believe
these results support our decision to advance EB-003 as our lead
candidate and pursue a development timeline intended to enable the
initiation of a clinical program and dosing of a first patient by
end of 2025.”
“Burdensome drug delivery methods, like injections, may not be
appealing to patients and can result in compliance challenges,
often leading to the discontinuation of treatment altogether,” said
Dr. Tucker. “Confirming that EB-003 can potentially be dosed orally
is an important milestone, and we believe supports our overarching,
patient-centered mindset, that non-hallucinogenic treatments must
have favorable pharmacological properties that support patient
adherence and reduce the treatment burden as they work to improve
their mental health.”
About Enveric Biosciences
Enveric Biosciences (NASDAQ: ENVB) is a biotechnology company
dedicated to the development of novel neuroplastogenic
small-molecule therapeutics for the treatment of depression,
anxiety, and addiction disorders. Leveraging its unique discovery
and development platform, Psybrary™, Enveric has created a robust
intellectual property portfolio of new chemical entities for
specific mental health indications. Enveric’s lead program, EB-003,
is a first-in-class approach to the treatment of
difficult-to-address mental health disorders designed to promote
neuroplasticity without inducing hallucinations in the patient.
Enveric is also developing EB-002, formerly EB-373, a next
generation synthetic prodrug of the active metabolite, psilocin,
being studied as a treatment of psychiatric disorders. Enveric is
headquartered in Naples, FL with offices in Cambridge, MA and
Calgary, AB Canada. For more information, please visit
www.enveric.com.
Forward-Looking Statements
This press release contains forward-looking statements and
forward-looking information within the meaning of applicable
securities laws. These statements relate to future events or future
performance. All statements other than statements of historical
fact may be forward-looking statements or information. Generally,
forward-looking statements and information may be identified by the
use of forward-looking terminology such as “plans,” “expects” or
“does not expect,” “proposes,” “budgets,” “explores,” “schedules,”
“seeks,” “estimates,” “forecasts,” “intends,” “anticipates” or
“does not anticipate,” or “believes,” or variations of such words
and phrases, or by the use of words or phrases which state that
certain actions, events or results may, could, should, would, or
might occur or be achieved. Forward-looking statements may include
statements regarding beliefs, plans, expectations, or intentions
regarding the future and are based on the beliefs of management as
well as assumptions made by and information currently available to
management. Actual results could differ materially from those
contemplated by the forward-looking statements as a result of
certain factors, including, but not limited to, the ability of
Enveric to: negotiate and finalize definitive agreements based on
the any of its out-licensing term sheets and perform pursuant to
the terms thereof; carry out successful clinical programs; achieve
the value creation contemplated by technical developments; avoid
delays in planned clinical trials; establish that potential
products are efficacious or safe in preclinical or clinical trials;
establish or maintain collaborations for the development of
therapeutic candidates; obtain appropriate or necessary
governmental approvals to market potential products; obtain future
funding for product development and working capital on commercially
reasonable terms; scale-up manufacture of product candidates;
respond to changes in the size and nature of competitors; hire and
retain key executives and scientists; secure and enforce legal
rights related to Enveric’s products, including patent protection;
identify and pursue alternative routes to capture value from its
research and development pipeline assets; continue as a going
concern; and manage its future growth effectively.
A discussion of these and other factors, including risks and
uncertainties with respect to Enveric, is set forth in Enveric’s
filings with the Securities and Exchange Commission, including
Enveric’s Annual Report on Form 10-K and its Quarterly Reports on
Form 10-Q. Enveric disclaims any intention or obligation to revise
any forward-looking statements, whether as a result of new
information, future events or otherwise, except as required by
law.
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version on businesswire.com: https://www.businesswire.com/news/home/20240725903859/en/
Investor Relations Tiberend Strategic Advisors, Inc.
David Irish (231) 632-0002 dirish@tiberend.com
Media Relations Tiberend Strategic Advisors, Inc. Casey
McDonald (646) 577-8520 cmcdonald@tiberend.com
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