Mayzent

siponimod · Novartis Europharm Limited
AUTHORISED IN THE EU

What Mayzent is used for

Mayzent is indicated for the treatment of adult patients with secondary progressive multiple sclerosis (SPMS) with active disease evidenced by relapses or imaging features of inflammatory activity.

Approved use, as published by the European Medicines Agency.

Key facts

Brand
Mayzent
Active substance
siponimod
Disease area
Multiple Sclerosis, Relapsing-Remitting
Medicine group
Selective immunosuppressants
ATC code
L04
Marketing authorisation holder
Novartis Europharm Limited
Authorised in the EU since
2020

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 Mayzent used for?

Mayzent is indicated for the treatment of adult patients with secondary progressive multiple sclerosis (SPMS) with active disease evidenced by relapses or imaging features of inflammatory activity.

What is the active substance in Mayzent?

Mayzent contains siponimod.

Who makes Mayzent?

The EU marketing authorisation holder is Novartis Europharm Limited.

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.