Thursday, July 4, 2013

U.S. FDA approves Biogen's multiple sclerosis drug, Tecfidera

March 27 (Reuters) - U.S. regulators have approved a new multiple sclerosis drug made by Biogen Idec Inc that is widely expected to become the No. 1 oral treatment for the disease, with annual sales of more than $3 billion.

Combined clinical trial data showed Tecfidera, formerly known as BG-12, cut the average relapse rate by 49 percent after two years compared to patients taking a placebo.

(Reporting By Toni Clarke in Washington; Editing by Tim Dobbyn)

((toni.clarke@thomsonreuters.com)(202-898-8340)(Reuters

Messaging: toni.clarke.thomsonreuters.com@reuters.net))

Keywords: BIOGEN TECFIDERA/


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