Europe OKs Biogen's Vumerity For Multiple Sclerosis

by Vandana Singh, Benzinga Editor

November 16, 2021 1:19 PM | 1 min read | Make a Comment

The European Commission has approved Biogen Inc's BIIB Vumerity (diroximel fumarate) to treat adults with relapsing-remitting multiple sclerosis (MS).
Vumerity is next-generation fumarate with the established efficacy and well-characterized safety of Tecfidera (dimethyl fumarate).
The approval was also based on findings from the EVOLVE-MS-2 Phase 3 study to evaluate the gastrointestinal (GI) tolerability of Vumerity compared to Tecfidera.
The rate of overall treatment discontinuation was lower in participants treated with Vumerity than those treated with Tecfidera (1.6% compared to 6%, respectively).
Price Action: BIIB shares are down 3.24% at $263 during the market session on the last check Tuesday.

Posted In: Biotech News Health Care FDA General Briefs multiple sclerosis

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