Omvoh

mirikizumab · Eli Lilly Nederland B.V.
AUTHORISED IN THE EU

What Omvoh is used for

Omvoh is indicated for the treatment of adult patients with moderately to severely active ulcerative colitis who have had an inadequate response with, lost response to, or were intolerant to either conventional therapy or a biologic treatment.

Approved use, as published by the European Medicines Agency.

Key facts

Brand
Omvoh
Active substance
mirikizumab
Disease area
Colitis, Ulcerative
Medicine group
Immunosuppressants
ATC code
L04AC
Marketing authorisation holder
Eli Lilly Nederland B.V.
Authorised in the EU since
2023

Official information

In the USA

Same active substance: Omvoh

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 Omvoh used for?

Omvoh is indicated for the treatment of adult patients with moderately to severely active ulcerative colitis who have had an inadequate response with, lost response to, or were intolerant to either conventional therapy or a biologic treatment.

What is the active substance in Omvoh?

Omvoh contains mirikizumab.

Who makes Omvoh?

The EU marketing authorisation holder is Eli Lilly Nederland B.V..

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.