Xeljanz now cleared for active psoriatic arthritis in EU

29 June 2018
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The European Commission has approved (tofacitinib citrate) 5mg twice daily (BID) in combination with methotrexate (MTX) for the treatment of active psoriatic arthritis (PsA) in adult patients who have had an inadequate response or who have been intolerant to a prior disease-modifying antirheumatic drug (DMARD) therapy.

US pharma giant Pfizer’s (NYSE: PFE) Xeljanz is the first and only oral Janus kinase (JAK) inhibitor to be approved in the European Union (EU) for the treatment of adults with active PsA.

In 2017, Xeljanz in combination with MTX was approved in the EU 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 DMARDs.

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