US FDA approves Bristol Myers Squibb’s Sotyktu (deucravacitinib) for the treatment of adults with active psoriatic arthritis

BMS

6 March 2026 - Significantly more patients treated with once daily, oral Sotyktu achieved an ACR20 response compared with placebo at week 16 in the pivotal Phase 3 POETYK PsA-1 and POETYK PsA-2 clinical trials.

Bristol Myers Squibb today announced that the US FDA has approved Sotyktu (deucravacitinib) for the treatment of adults with active psoriatic arthritis.

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Michael Wonder

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Michael Wonder

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Medicine , US , Dossier , Registration