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Cadence Pharmaceuticals Completes Enrollment of Pivotal Phase III Trial for Intravenous Acetaminophen Ahead of Schedule
Date:8/30/2007

nophen; the scope and validity of patent protection for IV acetaminophen; the company's ability to maintain patent protection for this product candidate and to commercialize it without infringing the patent rights of others; the market potential for pain, fever and other target markets, and the company's ability to compete with new or existing products; the company's ability to raise sufficient capital to complete its clinical development program for IV acetaminophen and to successfully launch this product candidate; and other risks detailed in Cadence's prior press releases as well as in Cadence's 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 registered 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


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SOURCE Cadence Pharmaceuticals, Inc.
Copyright©2007 PR Newswire.
All rights reserved

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