New River Pharmaceuticals Names Dr. Samir Roy Vice President, Formulation and Manufacturing
August 17 2006 - 5:03PM
PR Newswire (US)
RADFORD, Va., Aug. 17 /PRNewswire-FirstCall/ -- New River
Pharmaceuticals Inc. (NASDAQ:NRPH) announced today that Samir Roy,
Ph.D., has joined the company as Vice President, Formulation and
Manufacturing. Dr. Roy will operate from the company's laboratories
at the Virginia Tech Corporate Research Center in Blacksburg,
Virginia, and will report to Krish S. Krishnan, New River's Chief
Operating Officer. Krishnan remarked, "Dr. Roy is a strong addition
to New River, bringing the requisite skills and experience to
enhance our formulation and manufacturing capabilities. Our team
looks forward to working with him to advance our research and
development program." Immediately prior to joining New River, Dr.
Roy served as the Executive Director of Product Research at Watson
Pharmaceuticals Inc. In his nearly twenty years in the
pharmaceutical industry, he has held positions with Insite Vision
Inc., Pfizer-Agouron Pharmaceutical Inc., Roche Pharmaceuticals,
and Cygnus Therapeutics Inc. He has authored or co-authored more
than 25 journal articles, is listed on ten U.S. patents, and has
been involved in the development of a number of FDA product
approvals. Dr. Roy holds a Ph.D. degree from the College of
Pharmacy, University of Saskatchewan in Saskatoon, Canada, with a
research focus on the oral absorption of amphetamines and its
analogs. He conducted a post-doctoral fellowship at the University
of Michigan College of Pharmacy in Ann Arbor, Michigan, with a
research focus involving narcotic analgesics. He also holds a B.S.
degree in Pharmacy from the BHU Institute of Technology, India. Dr.
Roy commented, "I am excited to join the New River team to apply my
knowledge and experience to help realize the potential of the
company's Carrierwave(TM) technology." About New River New River
Pharmaceuticals Inc. is a specialty pharmaceutical company
developing novel pharmaceuticals that are generational improvements
of widely prescribed drugs in large and growing markets. For
further information on New River, please visit the Company's Web
site at http://www.nrpharma.com/. "SAFE HARBOR" STATEMENT UNDER THE
PRIVATE SECURITIES LITIGATION REFORM ACT OF 1995 This press release
contains certain forward-looking information that is intended to be
covered by the safe harbor for "forward-looking statements"
provided by the Private Securities Litigation Reform Act of 1995.
Forward- looking statements are statements that are not historical
facts. Words such as "expect(s)," "feel(s)," "believe(s)," "will,"
"may," "anticipate(s)" and similar expressions are intended to
identify forward-looking statements. These statements include, but
are not limited to, financial projections and estimates and their
underlying assumptions; statements regarding plans, objectives and
expectations with respect to future operations, products and
services; and statements regarding future performance. Such
statements are subject to certain risks and uncertainties, many of
which are difficult to predict and generally beyond the control of
New River Pharmaceuticals, that could cause actual results to
differ materially from those expressed in, or implied or projected
by, the forward-looking information and statements. These risks and
uncertainties include: those discussed and identified in the New
River Pharmaceuticals Inc. annual report on Form 10-K, filed with
the SEC on March 15, 2006; the timing, progress and likelihood of
success of our product research and development programs; the
timing and status of our preclinical and clinical development of
potential drugs; the likelihood of success of our drug products in
clinical trials and the regulatory approval process; our drug
products' efficacy, abuse and tamper resistance, resistance to
intravenous abuse, onset and duration of drug action, ability to
provide protection from overdose, ability to improve patients'
symptoms, incidence of adverse events, ability to reduce opioid
tolerance, ability to reduce therapeutic variability, and ability
to reduce the risks associated with certain therapies; the ability
to develop, manufacture, launch and market our drug products; our
projections for future revenues, profitability and ability to
achieve certain sales targets; our estimates regarding our capital
requirements and our needs for additional financing; the likelihood
of obtaining favorable scheduling and labeling of our drug
products; the likelihood of regulatory approval under the Federal
Food, Drug, and Cosmetic Act without having to conduct long and
costly trials to generate all of the data which are often required
in connection with a traditional new chemical entity; our ability
to develop safer and improved versions of widely prescribed drugs
using our Carrierwave(TM) technology; our success in developing our
own sales and marketing capabilities for our lead product
candidate, NRP104; and our ability to obtain favorable patent
claims. Readers are cautioned not to place undue reliance on these
forward-looking statements that speak only as of the date hereof.
New River Pharmaceuticals does not undertake any obligation to
republish revised forward-looking statements to reflect events or
circumstances after the date hereof or to reflect the occurrence of
unanticipated events. Readers are also urged to carefully review
and consider the various disclosures in New River Pharmaceuticals'
annual report on Form 10-K, filed with the SEC on March 15, 2006,
as well as other public filings with the SEC. Contacts: The Ruth
Group John Quirk (investors) 646-536-7029 Zack Kubow (media)
646-536-7020 DATASOURCE: New River Pharmaceuticals Inc. CONTACT:
Investors: John Quirk, +1-646-536-7029, , or Media: Zack Kubow,
+1-646-536-7020, , both of The Ruth Group, for New River
Pharmaceuticals Inc. Web site: http://www.nrpharma.com/
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