atai Life Sciences (NASDAQ: ATAI) (“atai”), a clinical-stage
biopharmaceutical company aiming to transform the treatment of
mental health disorders, announced positive results from its Phase
1 study evaluating orally administered EMP-01, the R-enantiomer of
MDMA (3,4-methylenedioxy-methamphetamine).
The goals of this Phase 1 study were to evaluate the safety,
tolerability, pharmacokinetics (PK), and pharmacodynamics (PD) of
EMP-01. The four-cohort, single-ascending dose, randomized,
double-blind, placebo-controlled study enrolled 32 healthy
participants who received 75mg, 125mg, 175mg or 225mg of EMP-01 or
placebo in a 6+2 design.
EMP-01 was well-tolerated, and treatment-related adverse events
(AEs) were all expected and generally dose dependent. There were no
study discontinuations, and no serious or severe AEs were observed
in the study. Non-clinically significant increases in blood
pressure and heart rate were observed, though such changes showed
limited dose dependency. Further, the peak body temperatures
observed fell within the normal range. Finally, bruxism was
observed in only 1 of 24 subjects that received EMP-01.
The PK profile of EMP-01 was dose-proportional. The PD measures
included both subjective reports and blood-based biomarkers.
Significant, consistent and dose-dependent changes were seen on
several of these exploratory PD measures. EMP-01 administration
resulted in a differentiated subjective experience compared to
racemic MDMA on standard psychedelic experience questionnaires.
Further, dose dependent changes on measures of emotional
breakthrough, a phenomenon thought to be a key mediator of the
long-term psychological changes associated with psychedelics, were
noted in this healthy volunteer population.
Detailed clinical data from the Phase 1 study of EMP-01 are
expected to be presented at a future medical meeting.
“I am grateful to the participants and investigators, as well as
the members of the atai study team on the successful completion of
this Phase 1 study,” said Florian Brand, CEO and Co-Founder of
atai. “Building upon the decades of research into MDMA as a
potential treatment for mental health disorders, including two
positive Phase 3 studies in PTSD, we are encouraged by the unique
characteristics of EMP-01 and exploring the implications for
further clinical development.”
“The two enantiomers of MDMA show markedly different and rich
pharmacology. The present study is one of the first specifically
focused on assessing the PK and PD of R-MDMA,” said Srinivas Rao,
CSO of atai. “We found differences in the subjective experience
R-MDMA in comparison to published reports involving racemic MDMA.
If confirmed, these differences suggest that R-MDMA may have
applicability in a broad array of mental conditions.”
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 EMP-01 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: our limited
operating history, historical losses, and anticipation that we will
continue to incur significant losses for the foreseeable future; we
will require substantial additional funding to achieve our business
goals, including the development and any commercialization of our
product candidates; we have never generated revenue and may never
be profitable; our product candidates contain controlled
substances, the use of which may generate public controversy;
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 and impact to such trials based on factors 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 and failure to
recruit and retain a sufficient number of therapists; the timing
and outcome of regulatory review and/or approvals, which are
necessary prior to commercialization; 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, including our loan
agreement with Hercules Capital, Inc.; our aggregate tax burden
based on our management 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, 2022, filed with the Securities and
Exchange Commission (“SEC”) and our quarterly reports on Form 10-Q,
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 InformationInvestor
Contact:ir@atai.life Media Contact:PR@atai.life
ATAI Life Sciences NV (NASDAQ:ATAI)
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