atai Life Sciences Announces Positive Topline Results from Beckley Psytech’s BPL-003 (intranasal 5-MeO-DMT benzoate) Phase 2a Open-Label Study for Alcohol Use Disorder
28 Janvier 2025 - 1:00PM
atai Life Sciences (NASDAQ: ATAI) (“atai” or “Company”), a
clinical-stage biopharmaceutical company aiming to transform the
treatment of mental health disorders, today announced positive
topline results from Beckley Psytech’s Phase 2a open-label study of
BPL-003 in 12 patients with moderate to severe alcohol use disorder
(AUD). BPL-003 is a patent-protected synthetic intranasal
formulation of 5-MeO-DMT benzoate designed to deliver rapid and
durable treatment effects from a single dose with a short in-clinic
treatment time. The results showed that a single dose of BPL-003,
in combination with relapse prevention cognitive behavioral
therapy, induced meaningful and sustained reduction in alcohol use
and heavy drinking days (HDDs) in patients with moderate to severe
AUD out to 12 weeks.
“We are encouraged by these exploratory results
from Beckley Psytech, our strategic investment, which demonstrate
the potential of short in-clinic psychedelic therapies to transform
the treatment of substance use disorders,” stated Dr. Srinivas Rao,
CEO and Co-founder of atai. “The high rates of sustained abstinence
in this study are particularly promising given the significant
challenges patients with alcohol use disorder face in achieving and
maintaining abstinence. These findings add to the growing body of
evidence supporting the potential of BPL-003 in treating serious
mental health disorders. We look forward to the Phase 2b data
readout of BPL-003 in treatment-resistant depression expected
mid-year.”
The 12-week Phase 2a open-label study enrolled
12 patients with moderate to severe AUD and evaluated the safety,
tolerability, pharmacodynamic effects and impact on alcohol use of
a single dose of BPL-003, in combination with relapse prevention
cognitive behavioral therapy (NCT05674929). The results
demonstrated meaningful and sustained reductions in alcohol use
following a single dose of BPL-003:
- Mean number of alcohol units
consumed per day decreased from 9.3 units to 2.2 units at Week
12
- Mean percentage of HDDs, defined as
consuming seven or more units of alcohol per day for women and nine
or more units of alcohol per day for men, declined from 56% to 13%
at Week 12
- Mean number of abstinent days
increased from 33% to 81% at Week 12
- 50% of the patients remained
completely abstinent through the 12-week study
BPL-003 was shown to be well-tolerated with
adverse events (AEs) being reported as mild or moderate and there
were no serious or severe adverse events reported. Most patients
were assessed as ready for discharge within approximately two
hours.
Beckley Psytech plans to evaluate future
development options for BPL-003 in substance use disorders and
anticipates reporting additional clinical data from this study in
publications and conferences in 2025.
About Alcohol Use Disorder
(AUD)AUD is a medical condition characterized by an
impaired ability to stop or control alcohol use despite adverse
social, occupational, or health consequences. The World Health
Organization estimates that around 400 million people suffer with
AUD worldwide, with around 3 million deaths each year attributed to
the harmful use of alcohol. Currently available pharmacological
treatment options are not very effective and some people with
alcohol use disorder who wish to abstain from, or reduce, alcohol
consumption do not achieve their treatment goal with currently
approved treatment options. This contributes to an unmet need for
more effective medical treatments.
About BPL-003 BPL-003 is
Beckley Psytech’s patent-protected synthetic intranasal 5-MeO-DMT
benzoate formulation, designed to deliver rapid and durable effects
from a single dose, with a short time in clinic. PL-003 is being
investigated for treatment resistant depression (TRD) and for
alcohol use disorder (AUD). In a Phase 2a study TRD study, a single
10mg dose of BPL-003 produced a rapid antidepressant response in
55% of patients at Day 1, with 55% of patients in remission at Day
29 and 45% in remission at Day 85. BPL-003 demonstrated a short
treatment duration, with patients deemed ready to be discharged
within an average of less than two hours. Topline Phase 2b data are
anticipated mid-2025.
About Beckley Psytech
LtdBeckley Psytech Ltd. is a private clinical-stage
biopharmaceutical company dedicated to improving the lives of
people with neuropsychiatric disorders through the development of
rapid-acting, short-duration psychedelic medicines. In January
2024, atai made a strategic investment in Beckley Psytech,
resulting in a 35.5% ownership stake and 1:1 warrant coverage at a
30% premium on the primary issuances. atai holds a time-limited
right of first refusal on a future sale of the company and an
indefinite right of first negotiation for BPL-003 and ELE-101. atai
and Beckley Psytech also agreed to collaborate on digital
therapeutics, commercial and market access activities in
preparation for future potential commercialization.
About atai Life Sciencesatai is
a clinical-stage biopharmaceutical company aiming to transform the
treatment of mental health disorders. The Company was founded in
response to the significant unmet need and lack of innovation in
the mental health treatment landscape. atai is dedicated to
developing novel, evidence-based therapeutics to treat depression,
anxiety and other mental health disorders. atai's vision is to heal
mental health disorders so that everyone, everywhere can live a
more fulfilled life. For more information, please
visit www.atai.life.
Forward-looking Statements This
press release contains forward-looking statements within the
meaning of the Private Securities Litigation Reform Act of 1995, as
amended. We intend such forward-looking statements to be covered by
the safe harbor provisions for forward-looking statements contained
in Section 27A of the Securities Act of 1933, as amended, and
Section 21E of the Securities Exchange Act of 1934, as amended. The
words “believe,” “may,” “will,” “estimate,” “continue,”
“anticipate,” “intend,” “expect,” “initiate,” “could,” “would,”
“project,” “plan,” “potentially,” “preliminary,” “likely,” and
similar expressions are intended to identify forward-looking
statements, although not all forward-looking statements contain
these words. All statements contained in this press release that do
not relate to matters of historical fact should be considered
forward-looking statements, including, without limitation,
statements relating to our business strategy and plans; and the
potential, success, cost and timing of development of our product
candidates, and the product candidates of those companies we invest
in, including the progress of preclinical and clinical trials and
related milestones such as BPL-003 and related data readouts.
Forward-looking statements are neither promises
nor guarantees, but involve known and unknown risks and
uncertainties that could cause actual results to differ materially
from those projected, including, without limitation, the factors
described in the section titled “Risk Factors” in our most recent
Annual Report on Form 10-K filed with the Securities and Exchange
Commission (SEC) on March 28, 2024, as such factors may be updated
from time to time in atai's other filings with the SEC. atai
disclaims any obligation or undertaking to update or revise any
forward-looking statements contained in this press release, other
than to the extent required by applicable law.
Contact InformationInvestor
Contact:IR@atai.life
Media Contact:PR@atai.life
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