AbbVie gains European nod for Rinvoq
Following a positive opinion from the European Medicines Agency’s advisory committee in October, the European Commission has granted approval for Rinvoq (upadacitinib) for the treatment of adult patients with moderate to severe active rheumatoid arthritis who have responded inadequately to, or who are intolerant to one or more disease-modifying anti-rheumatic drugs (DMARDs).
Developed by the USA’s AbbVie (NYSE: ABBV), Rinvoq is a once-daily selective and reversible JAK inhibitor and may be used as monotherapy or in combination with methotrexate (MTX). It was approved in the USA in August this year.
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