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EMA approval · 2026-08-06

EMA Authorised: Vumerity (Diroximel fumarate (BIIB098)) — Biogen Netherlands B.V.

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Summary

EMA has authorised Vumerity (diroximel fumarate) for relapsing-remitting multiple sclerosis, expanding Biogen's portfolio in this indication.

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Diseases / indications

Drugs mentioned

  • VUMERITY (diroximel fumarate)

Snippet

Status: Authorised. Therapeutic area: Multiple Sclerosis, Relapsing-Remitting. MAH: Biogen Netherlands B.V.. Decision date: 15/07/2026