FDA advisers say Sanofi's MS drug Lemtrada can be approved

11/14/2013 | PharmaTimes (U.K.) · Bloomberg

An FDA advisory committee said Sanofi's Lemtrada, or alemtuzumab, was not so risky that it precluded approval as a treatment for multiple sclerosis. The drug, however, should not be used for first-line treatment, the panel said. The agency is set to issue a decision by Dec. 27.

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PharmaTimes (U.K.) · Bloomberg

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