Uplizna

inebilizumab · Amgen Europe B.V.
AUTHORISED IN THE EU

What Uplizna is used for

Uplizna is indicated as monotherapy for the treatment of adult patients with neuromyelitis optica spectrum disorders (NMOSD) who are anti-aquaporin 4 immunoglobulin G (AQP4-IgG) seropositive (see section 5.1).

Approved use, as published by the European Medicines Agency.

Key facts

Brand
Uplizna
Active substance
inebilizumab
Disease area
Neuromyelitis Optica
Medicine group
Immunosuppressants
ATC code
L04AA
Marketing authorisation holder
Amgen Europe B.V.
Authorised in the EU since
2022

Official information

In the USA

Same active substance: Uplizna

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 Uplizna used for?

Uplizna is indicated as monotherapy for the treatment of adult patients with neuromyelitis optica spectrum disorders (NMOSD) who are anti-aquaporin 4 immunoglobulin G (AQP4-IgG) seropositive (see section 5.1).

What is the active substance in Uplizna?

Uplizna contains inebilizumab.

Who makes Uplizna?

The EU marketing authorisation holder is Amgen Europe 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.

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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.