Kevzara approved in Europe for rheumatoid arthritis

27 June 2017

The European Commission has granted marketing authorization for Kevzara (sarilumab) in combination with methotrexate (MTX) for the treatment of moderately to severely active rheumatoid arthritis (RA) in adult patients who have responded inadequately to - or who are intolerant to - one or more disease modifying anti-rheumatic drugs (DMARDs), such as MTX.

Developed by France’s Sanofi (Euronext: SAN) and USA-based Regeneron Pharmaceuticals (Nasdaq: REGN), Kevzara may be used as monotherapy in case of intolerance to MTX or when treatment with methotrexate is inappropriate.

Peak sales of $1 billion-plus have been projected for the drug. Kevzara received a positive opinion from the European Medicine Agency’s Committee for Medicinal Products for Human Use in April.

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