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FDA Approves BMS’ Sotyktu for Active Psoriatic Arthritis Treatment

The treatment is the first TYK2 inhibitor to be approved for PsA.

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By: Patrick Lavery

Content Marketing Editor

The U.S. FDA has approved Bristol Myers Squibb (BMS)’ Sotyktu (deucravacitinib) for treatment of adults with active psoriatic arthritis (PsA). Sotyktu is an oral, selective tyrosine kinase 2 (TYK2) inhibitor. According to BMS, Sotyktu is the first TYK2 inhibitor to be approved for PsA. PsA Defined and How Sotyktu Helps PsA can best be defined as a chronic, immune-mediated, heterogeneous disease that can have multiple musculoskeletal or skin manifestations. Among these symptoms may be infla...

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