with, or termination or disruption of the company's
relationships with, its contract manufacturers or suppliers; other
difficulties or delays in development, testing, manufacturing and marketing
of and obtaining regulatory approval for IV acetaminophen or Omigard; the
scope and validity of patent protection for IV acetaminophen or Omigard;
the company's ability to maintain patent protection for its product
candidates and to commercialize its product candidates without infringing
the patent rights of others; the market potential for pain, fever, local
catheter site infections and other target markets, and the company's
ability to compete; the potential to attract a strategic collaborator and
terms of any related transaction; the company's ability to raise sufficient
capital; and other risks detailed in Cadence's prior press releases as well
as in Cadence's periodic public filings with the Securities and Exchange
Commission.
You are cautioned not to place undue reliance on these forward-looking
statements, which speak only as of the date hereof. All forward-looking
statements are qualified in their entirety by this cautionary statement and
Cadence undertakes no obligation to revise or update this news release to
reflect events or circumstances after the date hereof. This caution is made
under the safe harbor provisions of Section 21E of the Private Securities
Litigation Reform Act of 1995.
Cadence(TM) and Omigard(TM) are trademarks of Cadence Pharmaceuticals,
Inc.
Contacts: William R. LaRue
SVP & Chief Financial Officer
Cadence Pharmaceuticals, Inc.
858-436-1400
Anna Gralinska
Director, Investor Relations
Cadence Pharmaceuticals, Inc.
858-436-1452
Susan Neath
Media Relations
Porter Novelli Life Sciences
619-849-6007
CADENCE PHARMACEUTI
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SOURCE Cadence Pharmaceuticals, Inc.
 Copyright©2007 PR Newswire. | |
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