PureTech Founded Entity Seaport Therapeutics Appoints David Wheadon, M.D., to its Board of Directors
13 August 2024 - 1:05PM
Business Wire
Prominent pharmaceutical leader from
AstraZeneca, Abbott, GlaxoSmithKline and Eli Lilly, brings
extensive regulatory affairs and clinical development expertise to
Seaport Board
PureTech Health plc (Nasdaq: PRTC, LSE: PRTC) ("PureTech" or the
"Company"), a clinical-stage biotherapeutics company, noted that
its Founded Entity, Seaport Therapeutics, a biopharmaceutical
company that is advancing novel neuropsychiatric medicines with a
proven strategy and team, today announced the appointment of David
Wheadon, M.D., to its Board of Directors. Dr. Wheadon is a
physician and psychiatrist with more than three decades of
experience in regulatory affairs, clinical strategy, and global
health policy at multinational companies across the pharmaceutical
industry.
The full text of the announcement from Seaport is as
follows:
Seaport Therapeutics Appoints David Wheadon,
M.D., to its Board of Directors
Prominent pharmaceutical leader from
AstraZeneca, Abbott, GlaxoSmithKline and Eli Lilly, brings
extensive regulatory affairs and clinical development expertise to
Seaport Board
BOSTON, August 13, 2024 – Seaport Therapeutics, a
clinical-stage biopharmaceutical company that is advancing novel
neuropsychiatric medicines with a proven strategy and team, today
announced the appointment of David Wheadon, M.D., to its Board of
Directors. Dr. Wheadon is a physician and psychiatrist with more
than three decades of experience in regulatory affairs, clinical
strategy, and global health policy at multinational companies
across the pharmaceutical industry.
“It is our pleasure to welcome David Wheadon to our Board of
Directors,” said Daphne Zohar, Founder and Chief Executive Officer
at Seaport. “David brings extensive regulatory expertise, and a
successful background in the development and approval of several
important neuropsychiatric medicines which will benefit Seaport as
we advance our clinical-stage pipeline of therapeutics for the
treatment of depression, anxiety and other neuropsychiatric
disorders.”
Dr. Wheadon is a distinguished pharmaceutical leader who most
recently served as Senior Vice President, Global Regulatory
Affairs, Patient Safety and Quality Assurance at AstraZeneca. While
at AstraZeneca, he drove regulatory strategy for the development
and approval of the company’s product portfolio and oversaw the
global regulatory affairs, patient safety and quality assurance
organization. Dr. Wheadon also served as a member of the company’s
Global Medicines Development Leadership team and Late-Stage Product
Committee, which was responsible for the progression of
AstraZeneca’s late-stage portfolio through clinical development,
regulatory approvals and market access.
“I’m excited to join the talented members of Seaport’s Board and
executive team with deep experience and a proven track record of
developing neuropsychiatric drugs,” said Dr. Wheadon. “Seaport has
a promising pipeline of novel antidepressants and anxiolytics, and
I look forward to being a part of the journey of delivering these
important new treatments to the millions of patients suffering from
devastating and debilitating mental health conditions, including
depression and anxiety.”
Dr. Wheadon held previous leadership positions at the
Pharmaceutical Research and Manufacturers of America (PhRMA), the
Juvenile Diabetes Research Foundation as well as senior regulatory
and clinical development leader roles at Abbott and
GlaxoSmithKline. He also served on the Board of Directors at Karuna
Therapeutics until its acquisition by Bristol Myers Squibb in March
2024. He began his career as a clinical research physician in
neuroscience at Eli Lilly. Dr. Wheadon earned an A.B. from Harvard
College and an M.D. from Johns Hopkins University School of
Medicine. His residency was in psychiatry at the Tufts-New England
Medical Center. He is a member of the American Academy of
Pharmaceutical Physicians and the American Psychiatric
Association.
“I had the privilege of working with David on the Karuna board,
so I know how incredibly fortunate we are to gain his unparalleled
level of expertise and industry perspective at Seaport,” said Steve
Paul, M.D., Founder and Chair of the Board of Directors at Seaport.
“He has an accomplished career and an astute understanding of the
regulatory and clinical landscape, which will make him a valuable
addition to Seaport as we continue to advance our novel
neuropsychiatric medicines through clinical development.”
About Seaport Therapeutics Seaport Therapeutics is a
clinical-stage biopharmaceutical company advancing the development
of novel neuropsychiatric medicines in areas of high unmet patient
needs. The Company has a proven strategy of advancing clinically
validated mechanisms previously held back by limitations that are
overcome with its proprietary Glyph™ technology platform. All the
therapeutic candidates in its pipeline of first and best-in-class
medicines are based on the Glyph platform, which is uniquely
designed to enable oral bioavailability, bypass first-pass
metabolism and reduce hepatotoxicity and other side effects.
Seaport is led by an experienced team that invented and advanced
important neuropsychiatric medicines and are guided by an extensive
network of renowned scientists, clinicians and key opinion leaders.
For more information, please visit www.seaporttx.com.
About PureTech Health PureTech is a clinical-stage
biotherapeutics company dedicated to giving life to new classes of
medicine to change the lives of patients with devastating diseases.
The Company has created a broad and deep pipeline through its
experienced research and development team and its extensive network
of scientists, clinicians and industry leaders that is being
advanced both internally and through its Founded Entities.
PureTech's R&D engine has resulted in the development of 29
therapeutics and therapeutic candidates, including two that have
received both U.S. FDA clearance and European marketing
authorization and a third (KarXT) that has been filed for FDA
approval. A number of these programs are being advanced by PureTech
or its Founded Entities in various indications and stages of
clinical development, including registration enabling studies. All
of the underlying programs and platforms that resulted in this
pipeline of therapeutic candidates were initially identified or
discovered and then advanced by the PureTech team through key
validation points.
For more information, visit www.puretechhealth.com or connect
with us on X (formerly Twitter) @puretechh.
Cautionary Note Regarding Forward-Looking Statements This
press release contains statements that are or may be
forward-looking statements within the meaning of the Private
Securities Litigation Reform Act of 1995. 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 those related to Seaport’s development plans for
its pipeline of therapeutics for the treatment of depression,
anxiety and other neuropsychiatric disorders, potential benefits to
patients and our future prospects, developments and strategies. The
forward-looking statements are based on current expectations and
are subject to known and unknown risks, uncertainties and other
important factors that could cause actual results, performance and
achievements to differ materially from current expectations,
including, but not limited to, those risks, uncertainties and other
important factors described under the caption "Risk Factors" in our
Annual Report on Form 20-F for the year ended December 31, 2023,
filed with the SEC and in our other regulatory filings. These
forward-looking statements are based on assumptions regarding the
present and future business strategies of the Company and the
environment in which it will operate in the future. Each
forward-looking statement speaks only as at the date of this press
release. Except as required by law and regulatory requirements, we
disclaim any obligation to update or revise these forward-looking
statements, whether as a result of new information, future events
or otherwise.
View source
version on businesswire.com: https://www.businesswire.com/news/home/20240812570975/en/
PureTech Public Relations
publicrelations@puretechhealth.com Investor Relations
IR@puretechhealth.com
UK/EU Media Ben Atwell, Rob Winder +44 (0) 20 3727 1000
puretech@fticonsulting.com
US Media Nichole Bobbyn +1 774 278 8273
nichole@tenbridgecommunications.com
PureTech Health (NASDAQ:PRTC)
Historical Stock Chart
Von Nov 2024 bis Dez 2024
PureTech Health (NASDAQ:PRTC)
Historical Stock Chart
Von Dez 2023 bis Dez 2024