CV Therapeutics Announces Presentations at the American Diabetes Association 68th Scientific Sessions
May 27 2008 - 5:01PM
PR Newswire (US)
PALO ALTO, Calif., May 27 /PRNewswire-FirstCall/ -- CV
Therapeutics, Inc. (NASDAQ:CVTX) announced today that two clinical
abstracts have been accepted for presentation at the American
Diabetes Association (ADA) 68th Scientific Sessions, which will be
held in San Francisco, CA on June 6 - 10, 2008. Ranexa(R)
(ranolazine extended-release tablets) Relationship Between
Nonfasting Plasma Glucose Concentrations and Improved Glycemic
Control in Patients with Diabetes and Coronary Artery Disease
Treated with Ranolazine; Poster; Sunday, June 8, 2008, 12:00 - 2:00
p.m. and 6:15 - 7:30 p.m. PDT Minority Angina Pectoris Patients at
High Risk for Diabetes and Metabolic Syndrome; Poster; Sunday, June
8, 2008, 12:00 - 2:00 p.m. and 6:15 - 7:30 p.m. PDT Additional
information regarding the ADA 68th Scientific Sessions can be
accessed at
http://professional.diabetes.org/Congress_Display.aspx?TYP=9&CID=58000.
About CV Therapeutics CV Therapeutics, Inc., headquartered in Palo
Alto, California, is a biopharmaceutical company primarily focused
on applying molecular cardiology to the discovery, development and
commercialization of novel, small molecule drugs for the treatment
of cardiovascular diseases. CV Therapeutics' approved products
include Ranexa(R) (ranolazine extended-release tablets), indicated
for the treatment of chronic angina in patients who have not
achieved an adequate response with other antianginal drugs, and
Lexiscan(TM) (regadenoson) injection for use as a pharmacologic
stress agent in radionuclide myocardial perfusion imaging in
patients unable to undergo adequate exercise stress. CV
Therapeutics also has other clinical and preclinical drug
development candidates and programs that have not been determined
to be safe or effective in humans for any uses. Except for the
historical information contained herein, the matters set forth in
this press release, including statements as to research and
development and commercialization of products, are forward-looking
statements within the meaning of the "safe harbor" provisions of
the Private Securities Litigation Reform Act of 1995. These
forward-looking statements are subject to risks and uncertainties
that may cause actual results to differ materially, including
operating losses and fluctuations in operating results; capital
requirements; regulatory review and approval of our products;
special protocol assessment agreement; the conduct and timing of
clinical trials; commercialization of products; market acceptance
of products; product labeling; concentrated customer base; reliance
on strategic partnerships and collaborations; uncertainties in drug
development; uncertainties regarding intellectual property and
other risks detailed from time to time in CV Therapeutics' SEC
reports, including its Quarterly Report on Form 10-Q for the
quarter ended March 31, 2008. CV Therapeutics disclaims any intent
or obligation to update these forward-looking statements.
DATASOURCE: CV Therapeutics, Inc. CONTACT: Investor and Media
Contact, John Bluth, Executive Director, Corporate Communications
& Investor Relations, CV Therapeutics, Inc., +1-650-384-8850
Web site: http://www.cvt.com/
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