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

nt of our registration program for IV acetaminophen in the United States," said James Breitmeyer, M.D., Ph.D., Executive Vice President, Development and Chief Medical Officer of Cadence. "With enrollment completed two months ahead of schedule, we are on track to announce top-line results of this study in early 2008, and we continue to make excellent progress with our other clinical trials of this product candidate."

About the IV Acetaminophen Clinical Development Program

Cadence's clinical development program for IV acetaminophen consists of three pivotal Phase III efficacy trials, two safety studies, and two pharmacokinetic studies, as set forth below:

Pivotal Phase III Efficacy Trials Enrollment Status

--------------------------------------------------------------------------

Treatment of pain following gynecologic surgery

(IV APAP 301 Study) Completed

Treatment of fever in adults Ongoing

Treatment of fever in adults comparing

intravenous and oral administration Ongoing

Other Trials Enrollment Status

--------------------------------------------------------------------------

Adult pharmacokinetics (1) Completed

Adult safety Initiation in Fourth

Quarter 2007

Pediatric pharmacokinetics Ongoing

Pediatric safety Initiation in Fourth

Quarter 2007

(1) The adult pharmacokinetics trial completed enrollment in December 2006

and preliminary results were presented at the April 2007 meeting of

the American Society of Regional Pain and Anesthesia.

The company anticipates com
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SOURCE Cadence Pharmaceuticals, Inc.
Copyright©2007 PR Newswire.
All rights reserved

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