Icotyde

icotrokinra hydrochloride · Janssen-Cilag International
AUTHORISED IN THE EU

What Icotyde is used for

Icotyde is indicated for the treatment of moderate to severe plaque psoriasis in adults, and adolescents 12 years of age and older and weighing at least 40 kg, who are candidates for systemic therapy

Approved use, as published by the European Medicines Agency.

Key facts

Brand
Icotyde
Active substance
icotrokinra hydrochloride
Disease area
Psoriasis
Medicine group
Immunosuppressants
ATC code
L04AC28
Marketing authorisation holder
Janssen-Cilag International
Authorised in the EU since
2026

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 Icotyde used for?

Icotyde is indicated for the treatment of moderate to severe plaque psoriasis in adults, and adolescents 12 years of age and older and weighing at least 40 kg, who are candidates for systemic therapy

What is the active substance in Icotyde?

Icotyde contains icotrokinra hydrochloride.

Who makes Icotyde?

The EU marketing authorisation holder is Janssen-Cilag International.

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

← All specialty medicines, EU

For information only, not medical advice. This page is a plain-language summary written from standard prescribing information and the public guides linked below. Brands sometimes change their formula, so always check the composition printed on the pack. Doses here are typical adult doses; yours may differ. Do not start, stop or change a medicine without your doctor or pharmacist, and keep all medicines away from children. In an emergency, call 112 (India) or your local emergency number.