Sotyktu

deucravacitinib · Bristol-Myers Squibb Pharma EEIG
AUTHORISED IN THE EU

What Sotyktu is used for

Plaque psoriasis Sotyktu is indicated for the treatment of moderate to severe plaque psoriasis in adults who are candidates for systemic therapy. Psoriatic arthritis Sotyktu, alone or in combination with methotrexate (MTX), is indicated for the treatment of active psoriatic arthritis (PsA) in adults who have had an inadequate response or who have been intolerant to a prior disease-modifying antirheumatic (DMARD) therapy.

Approved use, as published by the European Medicines Agency.

Key facts

Brand
Sotyktu
Active substance
deucravacitinib
Disease area
Psoriasis
Medicine group
Immunosuppressants
ATC code
L04AF07
Marketing authorisation holder
Bristol-Myers Squibb Pharma EEIG
Authorised in the EU since
2023

Official information

Specialist medicine: started and supervised by a specialist doctor or hospital. This page is a plain-language summary of public official information, not medical advice; follow your doctor and the official product information.

Common questions

What is Sotyktu used for?

Plaque psoriasis Sotyktu is indicated for the treatment of moderate to severe plaque psoriasis in adults who are candidates for systemic therapy. Psoriatic arthritis Sotyktu, alone or in combination with methotrexate (MTX), is indicated for the treatment of active psoriatic arthritis (PsA) in adults who have had an inadequate response or who have been intolerant to a prior disease-modifying antirheumatic (DMARD) therapy.

What is the active substance in Sotyktu?

Sotyktu contains deucravacitinib.

Who makes Sotyktu?

The EU marketing authorisation holder is Bristol-Myers Squibb Pharma EEIG.

Source: European Medicines Agency medicines data (ema.europa.eu), reproduced with acknowledgement of the source. Page made 5 November 2026 by Satya Babu.

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