Home » FDA Advisors Reject Sanofi’s Lemtrada As First-Line MS Therapy
FDA Advisors Reject Sanofi’s Lemtrada As First-Line MS Therapy
November 14, 2013
The FDA’s Peripheral and Central Nervous System Drugs Advisory Committee on Wednesday rejected Sanofi’s bid to expand the indication for its biologic Lemtrada to treat relapsing multiple sclerosis (MS).
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