Pfizer's Xeljanz (tofacitinib) receives marketing authorisation in the European Union for the treatment of active ankylosing spondylitis

Pfizer

18 November 2021 - Pfizer announced today that the European Commission has approved Xeljanz (tofacitinib) 5 mg twice daily for the treatment of adults with active ankylosing spondylitis who have responded inadequately to conventional therapy.

The approval of Xeljanz for ankylosing spondylitis is based on data from a Phase 3, multi-centre, randomised, double-blind, placebo-controlled trial that evaluated the efficacy and safety of tofacitinib 5 mg twice daily versus placebo in 269 adult patients living with active ankylosing spondylitis.

Read Pfizer press release 

Michael Wonder

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Michael Wonder

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Outcome , Medicine , Europe