atai Life Sciences (NASDAQ: ATAI) (“atai” or “Company”), a
clinical-stage biopharmaceutical company aiming to transform the
treatment of mental health disorders, today announced the
publication of the Phase 1 results of BPL-003, Beckley Psytech’s
novel, synthetic, intranasal benzoate salt formulation of
5-MeO-DMT, in The Journal of Psychopharmacology.
The double-blind, placebo-controlled, single
ascending dose Phase 1 study explored the safety, tolerability,
pharmacokinetics (PK) and pharmacodynamics (PD) of BPL-003 in
combination with psychological support in 44 psychedelic-naïve
healthy volunteers. Participants across seven cohorts were given
either a single dose of BPL-003 between 1 mg to 12 mg or a
placebo.
The paper shows that BPL-003 was safe and
well-tolerated with no serious or severe adverse events reported.
BPL-003 was rapidly absorbed and eliminated, with 5-MeO-DMT
systemic exposure increasing approximately dose‑proportionally.
There was a reliable onset of subjective psychedelic effects within
minutes, which resolved in less than two hours. If confirmed in
larger studies, these findings could support a scalable single dose
treatment model fitting within the existing interventional
treatment paradigm.
The intensity of the subjective psychedelic
experience was shown to correlate with exposure to the compound.
The PD endpoint scores of the Mystical Experience Questionnaire
(MEQ-30) and Ego Dissolution Inventory (EDI) increased with an
increase in the BPL-003 dose. Sixty percent of participants had a
‘complete mystical experience,’ which is defined as reaching or
exceeding a score of three on all four subdomains of the MEQ-30
scale, at 10 mg and 12 mg doses of BPL-003. Notably, 87% of
participants who received BPL-003 said they would accept the same
or higher dose again, with 100% of participants who received the
highest (12 mg) dose stating they would accept the same or higher
dose again.
Commenting on the publication, Florian Brand,
CEO and Co-Founder of atai, said: “We are pleased by the
publication of the BPL-003 Phase 1 data in the Journal of
Psychopharmacology, a well-regarded, peer-reviewed journal.
Consistent with the initial Phase 2a data reported recently, the
Phase 1 results showed that BPL-003 was safe and well-tolerated and
underscore its potential as a scalable interventional treatment
requiring two hours or less in the clinic, in line with the
treatment paradigm successfully established by Spravato®.”
BPL-003 is currently under investigation in
Phase 2a studies as a potential treatment for Alcohol Use Disorder
(NCT05674929) and Treatment Resistant Depression (TRD)
(NCT05660642). It is also being explored in a multi-site Phase 2b
study (NCT05870540) for TRD. The trial is evaluating the effects of
a single, medium, or high dose of BPL-003 against a sub-perceptual
dose in TRD patients not taking concomitant antidepressants.
Initial results from that study are expected in H2 2024.
About Beckley Psytech and
BPL-003
Beckley Psytech is a private clinical-stage
biopharmaceutical company developing BPL-003, which is 5-MeO-DMT, a
short-duration psychedelic tryptamine that binds to a variety of
serotonergic receptors. Epidemiological surveys and observational
studies have reported that 5-MeO-DMT is associated with
improvements in mood, anxiety, reduced stress, increased life
satisfaction and mindfulness. 5-MeO-DMT has been reported to
produce mystical experiences with comparative intensity as seen
with high doses of psilocybin but has a significantly shorter
duration of effect.
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 Sciences
atai is a clinical-stage biopharmaceutical
company aiming to transform the treatment of mental health
disorders and was founded as a response to the significant unmet
need and lack of innovation in the mental health treatment
landscape. atai is dedicated to efficiently developing innovative
therapeutics to treat depression, anxiety, addiction, and other
mental health disorders. By pooling resources and best practices,
atai aims to responsibly accelerate the development of new
medicines to achieve clinically meaningful and sustained behavioral
change in mental health patients. 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. The words “believe,” “may,” “will,” “estimate,” “continue,”
“anticipate,” “intend,” “expect,” “could,” “would,” “project,”
“plan,” “potentially,” “preliminary,” “likely,” and the negative of
these terms and similar expressions are intended to identify
forward-looking statements, though not all forward-looking
statements use these words or expressions. All statements contained
in this press release other than statements of historical fact
should be considered forward-looking statements, including without
limitation our expectations and projections regarding the success,
potential uses and timing of development of BPL-003 and related
trials and studies, and our business strategy and plans.
Because forward-looking statements are subject to risks and
uncertainties, actual results may differ materially from those
expressed or implied by such forward-looking statements. These
risks and uncertainties include, among others: clinical and
preclinical development is uncertain, and our programs may
experience delays or may never advance to clinical trials; our
reliance on third parties to assist in conducting our clinical
trials including failure by third parties to meet trial or testing
deadlines; our reliance on qualified therapists working at
third-party clinical trial sites to administer certain of our
product candidates; the timing and outcome of regulatory review
and/or approvals; research and development of drugs targeting the
central nervous system, or CNS, is particularly difficult, and it
can be difficult to predict and understand why a drug has a
positive effect on some patients but not others; significant
competition; obtaining, maintaining and protecting our intellectual
property; restricted operating activity as a result of covenants in
any financing arrangements; and operational activity. These
forward-looking statements are subject to a number of important
factors that could cause actual results to differ materially from
those in the forward-looking statements, including the risks,
uncertainties, and assumptions described in our Form 10-K for the
year ended December 31, 2023, filed with the Securities and
Exchange Commission (“SEC”), as may be updated by other filings we
file with or furnish to the SEC.
Any forward-looking statements made herein speak
only as of the date of this press release. Except as required by
applicable law, we undertake no obligation to update any of these
forward-looking statements for any reason after the date of this
press release or to conform these statements to actual results or
revised expectations.
Contact Information
Investor Contact:
IR@atai.life
Media Contact:
PR@atai.life
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