Data from EMC - Curated by Toby Galbraith - Last updated 16 March 2017

Licensing authority

EMA (European Medicines Agency)


Olumiant is indicated for the treatment of moderate to severe active rheumatoid arthritis in adult patients who have responded inadequately to, or who are intolerant to one or more disease-modifying anti-rheumatic drugs. Olumiant may be used as monotherapy or in combination with methotrexate.

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Category Value
Agency product number EMEA/H/C/004085
Orphan designation No
Date First Approved 13-02-2017
Type POM
Marketing authorisation holder Eli Lilly Nederland B.V.