FDA approves Bristol Myers’ Sotyktu in new indication

9 March 2026

The US Food and Drug Administration (FDA) has approved pharma major Bristol Myers Squibb’s (NYSE; BMY) Sotyktu (deucravacitinib) for the treatment of adults with active psoriatic arthritis (PsA). Sotyktu, an oral, selective tyrosine kinase 2 (TYK2) inhibitor, is the first TYK2 inhibitor to be approved for PsA.

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