BMS wins EU approval for Sotyktu to treat active psoriatic arthritis in adults

بريستول مايرز سكويب كو

Bristol-Myers Squibb Company

BMY

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  • European Commission granted marketing authorization for Sotyktu (deucravacitinib) to treat active psoriatic arthritis in adults with inadequate response or intolerance to prior DMARD therapy.
  • Label covers use as monotherapy or with methotrexate; drug is once-daily oral TYK2 inhibitor.
  • Approval backed by Phase 3 POETYK PsA-1 and PsA-2 trials, which met primary endpoint with ACR20 responses at Week 16 versus placebo.


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