atai Life Sciences (NASDAQ: ATAI) (“atai”), a clinical-stage
biopharmaceutical company focused on developing innovative
therapies for neuropsychiatric diseases and its subsidiary,
Perception Neuroscience (“Perception”), today announced the
completion of enrollment of its Phase 2a clinical trial to evaluate
the safety and efficacy of a single intravenous infusion (IV) dose
of PCN-101 (R-ketamine). R-ketamine is a stereoisomer of ketamine
being developed for treatment-resistant depression (TRD). TRD
patients are partially or entirely unresponsive to antidepressants
and face issues of misdiagnosis, prolonged depressive periods,
co-occurring mental and physical disorders, and longer periods with
a lower quality of life than patients suffering from less severe
depression.
The Phase 2a proof-of-concept trial is a randomized,
double-blind, placebo-controlled study with an enrollment target of
93 TRD patients across three arms. The last patient is expected to
be dosed this week, with the total number of patients expected to
be around 100. These patients – all of whom had previously failed
at least two rounds of antidepressants – received either a single
dose of placebo, 30 mg, or 60 mg of PCN-101 via IV in addition to
their existing treatment regimen. Patients were assessed for a
change in depressive symptomatology using the Montgomery-Asberg
Depression Rating Scale (MADRS) at intervals over 14 days, with the
primary endpoint at 24 hours post-dose. Dissociation and sedation
were measured using the Clinician-Administered Dissociative States
Scale (CADSS) and the Modified Observer’s Alertness/Sedation Scale
(MOAA/S), respectively.
“This is a critical study and the first to assess the efficacy,
tolerability, and duration of action of PCN-101 in a double-blind
manner. We look forward to sharing the topline results around
year-end,” said Maju Mathews, MD, Chief Medical Officer of
Perception. “We are working diligently to initiate our next study
comparing the intravenous to the subcutaneous formulation.”
“I am very proud of the Perception team and our partners for
reaching this critical milestone in our program to explore the
potential of PCN-101 for people living with TRD. In addition, I am
grateful to the patients who took the time and effort to
participate in the study,” said Terence Kelly, Ph.D., CEO of
Perception Neuroscience. “An estimated 100 million people worldwide
live with TRD. These patients are more likely than those with
milder depression to experience serious complications, ranging from
physical comorbidities to suicidal ideation and suicide attempts.
PCN-101 has the potential to offer those with TRD a rapid-acting
antidepressant that can be administered in the home.”
“Completing enrollment of this Phase 2a trial is an important
achievement and represents a major step towards potentially
delivering a novel care option for mental health patients with
unsupervised, at-home administration,” added Florian Brand,
Co-Founder, and CEO of atai Life Sciences. “Changing the treatment
landscape for TRD may not only alleviate the suffering of the 100
million people living with TRD around the globe, but also decrease
overall healthcare utilization, bringing us closer to realizing our
vision of healing mental health disorders so that everyone,
everywhere can live a more fulfilled life.”
atai will be hosting a virtual R&D Day today, October 25, at
12 pm ET, during which it will discuss the PCN-101 program and
contextualize the upcoming Phase 2a readout, among other topics.
Click here or visit our website for more information:
https://ir.atai.life/news-events/events.
About PCN-101Perception Neuroscience is
developing PCN-101 (R-ketamine) for the treatment of
treatment-resistant depression. PCN-101 is a single isomer of
ketamine and belongs to a new generation of glutamate receptor
modulators with the potential for rapid-acting antidepressant
(RAAD) activity and anti-suicidal effects. Pharmacologically,
PCN-101 is a non-competitive N-methyl-D-aspartate (NMDA) receptor
antagonist. Nonclinical depression model studies in rodents suggest
that R-ketamine could possess more durable and potent effects than
S-ketamine despite a lower affinity to the NMDA receptor and
potentially a more favorable safety and tolerability profile.
About Perception Neuroscience, IncPerception
Neuroscience is a New York City-based clinical-stage
biopharmaceutical company committed to developing therapies for
neuropsychiatric diseases. Perception’s mission is to provide more
effective treatment solutions for serious psychiatric disorders.
The company is a majority-owned subsidiary of atai Life
Sciences.
About atai Life Sciencesatai Life Sciences is a
clinical-stage biopharmaceutical company aiming to transform the
treatment of mental health disorders. Founded in 2018 as a response
to the significant unmet need and lack of innovation in the mental
health treatment landscape, atai is dedicated to acquiring,
incubating, and 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 across its
companies 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 StatementsThis press release
contains forward-looking statements within the meaning of the
Private Securities Litigation Reform Act of 1995, 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. Forward-looking statements include express or implied
statements relating to, among other things: statements regarding
the trials by Perception Neuroscience and future results and
activities thereunder; the potential of PCN-101; the success, cost
and timing of development of our product candidates, including the
progress of preclinical and clinical trials and related milestones;
our business strategy and plans; potential acquisitions; and the
plans and objectives of management for future operations and
capital expenditures. The forward-looking statements in this press
release are neither promises nor guarantees, and you should not
place undue reliance on these forward-looking statements because
they involve known and unknown risks, uncertainties, and other
factors, many of which are beyond our control and which could cause
actual results, levels of activity, performance, or achievements to
differ materially from those expressed or implied by these
forward-looking statements.
The forward-looking statements in this press release are neither
promises nor guarantees, and you should not place undue reliance on
these forward-looking statements. These forward-looking statements
are subject to a number of risks, uncertainties, and assumptions
that could cause actual results to differ materially from those
expressed or implied by the forward-looking statements, including
without limitation: we are a clinical-stage biopharmaceutical
company and have incurred significant losses since our inception,
and we anticipate that we will continue to incur significant losses
for the foreseeable future; we will require substantial additional
funding to achieve our business goals, and if we are unable to
obtain this funding when needed and on acceptable terms, we could
be forced to delay, limit or terminate our product development
efforts; our limited operating history may make it difficult to
evaluate the success of our business and to assess our future
viability; we have never generated revenue and may never be
profitable; clinical and preclinical development is uncertain, and
our preclinical programs may experience delays or may never advance
to clinical trials; we rely on third parties to assist in
conducting our clinical trials and some aspects of our research and
preclinical testing, and those clinical trials, including progress
and related milestones, may be impacted by several factors
including the failure by such third parties to meet deadlines for
the completion of such trials, research, or testing, changes to
trial sites and other circumstances; we cannot give any assurance
that any of our product candidates will receive regulatory
approval, which is necessary before they can be commercialized;
third parties may claim that we are infringing, misappropriating or
otherwise violating their intellectual property rights, the outcome
of which would be uncertain and may prevent or delay our
development and commercialization efforts; and a pandemic,
epidemic, or outbreak of an infectious disease, such as the
COVID-19 pandemic, may materially and adversely affect our
business, including our preclinical studies, clinical trials, third
parties on whom we rely, our supply chain, our ability to raise
capital, our ability to conduct regular business and our financial
results. These and other important factors described in the section
titled “Risk Factors” in our Annual Report on Form 10-K for the
fiscal year ended December 31, 2021, filed with the Securities and
Exchange Commission (“SEC”), our Quarterly Reports on Form 10-Q and
our Current Reports on Form 8-K, as updated by our subsequent
filings with the SEC, may cause our actual results, performance, or
achievements to differ materially and adversely from those
expressed or implied by the forward-looking statements. Any such
forward-looking statements represent management’s estimates as of
the date of this press release. While we may elect to update such
forward-looking statements at some point in the future, we disclaim
any obligation to do so, even if subsequent events cause our views
to change.
Contact Information
Investor Contact:Stephen BardinChief Financial
OfficerIR@atai.life
Media Contact:Allan MalievskySenior Director, External
AffairsPR@atai.life
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