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News   Drug Development

U.S. FDA Postpones Schering-Plough Corporation Panel for Melanoma

March 10, 2008 | 
1 min read
WASHINGTON (Reuters) - A U.S. Food and Drug Administration advisory panel to review the use of Schering-Plough Corp's Pegintron drug to treat serious skin cancer has been postponed, the company said on Monday.
Clinical research Postmarket research
Food and Drug Administration (FDA)
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