Neurobiological Technologies Names David E. Levy, M.D., As Vice President of Clinical Development to Lead Viprinex(TM) Team
August 23 2004 - 9:45AM
PR Newswire (US)
Neurobiological Technologies Names David E. Levy, M.D., As Vice
President of Clinical Development to Lead Viprinex(TM) Team
RICHMOND, Calif., Aug. 23 /PRNewswire-FirstCall/ -- Neurobiological
Technologies, Inc. (NTI(R)) (NASDAQ:NTII) today announced that on
September 1, 2004, David E. Levy, M.D., will join the company as
vice president of clinical development, a newly created position.
Initially, Dr. Levy will lead the clinical development effort for
Viprinex(TM) (ancrod), a late-stage reperfusion therapy for use in
the treatment of acute ischemic stroke. NTI obtained rights to
Viprinex through its acquisition of Empire Pharmaceuticals in July
2004. "Viprinex was initially developed by Knoll Pharmaceuticals,
where Dr. Levy was in charge of the clinical program. He has
extensive experience in the area of stroke therapy and comes to NTI
with expertise successfully directing major clinical programs in
CNS," said Paul E. Freiman, Neurobiological Technologies' president
and chief executive officer. "We believe David is ideally suited to
help lead NTI's stroke program and our planned Viprinex Phase III
clinical trials, as well as other clinical efforts at the company.
We expect that he will be a tremendous asset to NTI and we are
delighted that he will be joining our team." Levy joins NTI after
14 years in the pharmaceutical industry preceded by an illustrious
academic career. Most recently, he was international project team
leader at Eisai Medical Research, Inc. where he directed a clinical
program to develop a novel, new therapy in Alzheimer's disease as
well as acute ischemic stroke programs. Previously, he served as an
advisor to Empire Pharmaceuticals and as senior director of medical
research at DOV Pharmaceutical, where he directed several clinical
development programs. From 1991 to 2001, Dr. Levy was with Knoll
Pharmaceuticals, serving initially as senior director and
therapeutic head of clinical CNS and then as senior director of
cardiovascular/internal medicine. At Knoll, he directed the group
that designed and conducted one of the world's only successful
therapeutic studies of acute ischemic stroke. Dr. Levy's academic
career includes 23 years at Weill-Cornell Medical College and New
York Presbyterian Hospital, where he was an intern and resident
from 1968 through 1970 and served as executive vice chair of
neurology from 1988 to 1991. He continues to serve as adjunct
associate professor of neurology and adjunct associate attending
neurologist at these institutions. He is certified by the American
Board of Psychiatry and Neurology, the American Board of Internal
Medicine, and is licensed to practice medicine in New York State.
Among his professional affiliations, Levy is a fellow of the
American Academy of Neurology, the American College of Physicians,
and the Stroke Counsel of the American Heart Association. He is
widely published in the areas of cerebrovascular disease, including
ischemic stroke and central nervous system disorders. Levy earned
his bachelor of arts degree in chemistry and physics, cum laude,
from Harvard College and his doctor of medicine degree from Harvard
Medical School. About Neurobiological Technologies, Inc. (NTI) NTI
is an emerging drug development company focused on the clinical
evaluation and regulatory approval of neuroscience drugs. The
company's strategy is to in-license and develop early- and
later-stage drug candidates that target major medical needs and
that can be rapidly commercialized. Its management team oversees
the human clinical trials necessary to establish preliminary
evidence of efficacy and seeks partnerships with pharmaceutical and
biotechnology companies to complete development and marketing of
its product candidates. Except for the historical information
contained herein, the matters discussed in this press release are
forward-looking statements that involve risks and uncertainties,
including, but not limited to, our ability to develop and meet
regulatory requirements for our products, including Viprinex, the
inherent risk of failure in developing product candidates based on
new technologies, the risks of acquiring companies and new
technologies and other risks detailed from time to time in the
Company's Securities and Exchange Commission filings. Actual
results may differ materially from those projected. These
forward-looking statements represent management's judgment as of
the date of this release. The company disclaims, however, any
intent or obligation to update these forward-looking statements.
DATASOURCE: Neurobiological Technologies, Inc. CONTACT: Paul E.
Freiman, President & CEO of Neurobiological Technologies, Inc.,
+1-510-262-1730; or Roger Pondel or Rob Whetstone, both of
PondelWilkinson Inc., +1-310-279-5980, for Neurobiological
Technologies, Inc. Web site: http://www.ntii.com/
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