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FDA Denies Approval for Lemtrada (Alemtuzumab)

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    FDA Denies Approval for Lemtrada (Alemtuzumab)

    The U.S. Food and Drug Administration has denied approval at this time for Lemtrada™ (alemtuzumab, Genzyme, a Sanofi Company) as a therapy for relapsing MS. According to a company press release, the FDA has taken the position that one or more additional clinical trials would be needed for marketing approval of Lemtrada. The company plans to appeal the agency’s decision.

    To read this full article, click here.
    National MS Society December 30, 2013
    Ashley Ringstaff
    Ringer1319/RingpOP
    MSWorld Volunteer
    Living with MS since 8/30/10
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