MindMed Appoints Javier Muniz, M.D., as Vice President of Research and Development Strategy
03 Dezember 2024 - 1:00PM
Business Wire
Mind Medicine (MindMed) Inc. (NASDAQ: MNMD), (the "Company" or
"MindMed"), a clinical-stage biopharmaceutical company developing
novel product candidates to treat brain health disorders, today
announced the appointment of Javier A. Muniz, M.D., as Vice
President of Research and Development (R&D) Strategy. In his
new role, Dr. Muniz will drive innovation and growth of MindMed’s
R&D operations as the Company prepares to initiate three Phase
3 studies of MM120 orally disintegrating tablet (ODT) in
generalized anxiety disorder and major depressive disorder.
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Javier Muniz, M.D. - Vice President of
Research and Development Strategy, MindMed (Photo: Business
Wire)
“Javier’s extensive expertise leading interdisciplinary
scientific teams at the U.S. Food and Drug Administration (FDA),
combined with his deep experience within the uniformed services in
the fields of neuroscience and psychiatry makes him a welcome
addition to the MindMed team,” said Dan Karlin, M.D., M.A., Chief
Medical Officer of MindMed. “His leadership will play an important
role in strengthening our R&D operations as we advance the
therapeutic potential of our pipeline, prepare for two potential
approvals and aim to reshape the treatment landscape for people
living with brain health disorders.”
Dr. Muniz will report to Dr. Karlin.
“I am thrilled to join MindMed at such a pivotal moment in the
Company’s history, with potential approvals of MM120 ODT for
multiple indications on the horizon,” said Dr. Muniz. “The
groundbreaking science and purpose-driven culture made this a
unique and compelling opportunity. I look forward to advancing our
pipeline and ushering in psychedelics as a potential
transformational treatment paradigm in psychiatry.”
Javier A. Muniz, M.D.
Dr. Muniz is an expert in psychiatry, regulatory science, and
drug development, with more than 20 years of experience in the
uniformed services. He served 11 years at the FDA as a member of
the U.S. Public Health Service, where he held roles including
clinical team leader, associate director, acting deputy director,
and supervisory health scientist. He provided regulatory oversight
for innovative psychiatric drug development programs, including
first-in-class treatments, the first “digital” pill, and
breakthrough therapy-designated programs. He also co-authored
several guidance for industry documents.
Dr. Muniz is a recognized thought leader in psychedelic and
entactogen-based therapies, having presented at numerous national
and international conferences on scientific and regulatory
challenges. Before the FDA, he served in the U.S. Air Force,
directing psychiatric programs at Andrews Air Force Base, and Fort
Meade, MD, where he supported national security missions, led
rapid-response teams for the U.S. Department of Health and Human
Services, and provided care to Wounded Warriors.
Dr. Muniz completed his undergraduate and medical degrees in
Puerto Rico and his psychiatry residency at Mount Sinai Medical
Center in New York City. He is board-certified in psychiatry and
has received numerous awards, including two Presidential Unit
Citations, the Meritorious Service Medal, and the Afghanistan
Campaign Medal.
About MindMed
MindMed is a clinical-stage biopharmaceutical company developing
novel product candidates to treat brain health disorders. Our
mission is to be the global leader in the development and delivery
of treatments that unlock new opportunities to improve patient
outcomes. We are developing a pipeline of innovative product
candidates, with and without acute perceptual effects, targeting
neurotransmitter pathways that play key roles in brain health.
MindMed trades on NASDAQ under the symbol MNMD.
Forward-Looking Statements
Certain statements in this news release related to the Company
constitute "forward-looking information" within the meaning of
applicable securities laws and are prospective in nature.
Forward-looking information is not based on historical facts, but
rather on current expectations and projections about future events
and are therefore subject to risks and uncertainties which could
cause actual results to differ materially from the future results
expressed or implied by the forward-looking statements. These
statements generally can be identified by the use of
forward-looking words such as "will", "may", "should", "could",
"intend", "estimate", "plan", "anticipate", "expect", "believe",
"potential" or "continue", or the negative thereof or similar
variations. Forward-looking information in this news release
includes, but is not limited to, statements regarding the Company’s
anticipated upcoming milestones, trials and studies; and the
potential benefits of the Company’s product candidates. There are
numerous risks and uncertainties that could cause actual results
and the Company's plans and objectives to differ materially from
those expressed in the forward-looking information, including
history of negative cash flows; limited operating history;
incurrence of future losses; availability of additional capital;
compliance with laws and regulations; difficulty associated with
research and development; risks associated with clinical trials or
studies; heightened regulatory scrutiny; early stage product
development; clinical trial risks; regulatory approval processes;
novelty of the psychedelic inspired medicines industry; as well as
those risk factors discussed or referred to herein and the risks
described in the Company's Annual Report on Form 10-K for the
fiscal year ended December 31, 2023 under headings such as "Special
Note Regarding Forward-Looking Statements," and "Risk Factors" and
"Management's Discussion and Analysis of Financial Condition and
Results of Operations" and other filings and furnishings made by
the Company with the securities regulatory authorities in all
provinces and territories of Canada which are available under the
Company's profile on SEDAR+ at www.sedarplus.ca and with the U.S.
Securities and Exchange Commission on EDGAR at www.sec.gov. Except
as required by law, the Company undertakes no duty or obligation to
update any forward-looking statements contained in this release as
a result of new information, future events, changes in expectations
or otherwise.
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