VUMERITY (diroximel fumarate)

Woman sitting in wheelchair in hospital room

European Commission grants marketing authorisation for Vumerity^®

17 November 2021 | By Anna Begley (European Pharmaceutical Review)

The European Commission (EC) has granted marketing authorisation for Vumerity® to treat adults with relapsing-remitting multiple sclerosis.

news

EMA’s human medicines committee (CHMP) September meeting highlights

20 September 2021 | By Anna Begley (European Pharmaceutical Review)

In its most recent meeting, the CHMP recommended nine new medicines and concluded its review of Vaxzevria’s thrombosis risk.

news

Relapsing multiple sclerosis drug approved by FDA

31 October 2019 | By Victoria Rees (European Pharmaceutical Review)

VUMERITY has been granted approved by the FDA for the treatment of relapsing forms of multiple sclerosis based on data from a New Drug Application submission.

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VUMERITY (diroximel fumarate)

European Commission grants marketing authorisation for Vumerity®

EMA’s human medicines committee (CHMP) September meeting highlights

Relapsing multiple sclerosis drug approved by FDA

European Commission grants marketing authorisation for Vumerity^®