TECFIDERA (dimethyl fumarate)

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

28 February 2022 | By European Pharmaceutical Review

Highlights of the February 2022 meeting of EMA’s human medicines committee (CHMP) include the recommendation of 13 medicines for approval, along with updates to other drugs and COVID-19 vaccines.

Woman sitting in wheelchair in hospital room

news

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

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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TECFIDERA (dimethyl fumarate)

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

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