Agamree

vamorolone · Santhera Pharmaceuticals (Deutschland) GmbH
ORPHAN AUTHORISED IN THE EU

What Agamree is used for

Agamree is indicated for the treatment of Duchenne muscular dystrophy (DMD) in patients aged 2 years and older.

Approved use, as published by the European Medicines Agency.

What the labels mean

  • Orphan medicine: for a rare disease (affecting no more than 5 in 10,000 people in the EU).

Key facts

Brand
Agamree
Active substance
vamorolone
Disease area
Muscular Dystrophy, Duchenne
Medicine group
Glucocorticoids
ATC code
H02AB18
Marketing authorisation holder
Santhera Pharmaceuticals (Deutschland) GmbH
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 Agamree used for?

Agamree is indicated for the treatment of Duchenne muscular dystrophy (DMD) in patients aged 2 years and older.

What is the active substance in Agamree?

Agamree contains vamorolone.

Who makes Agamree?

The EU marketing authorisation holder is Santhera Pharmaceuticals (Deutschland) GmbH.

Is Agamree an orphan medicine?

Yes. Agamree is designated an orphan medicine in the EU, for a rare disease (Muscular Dystrophy, Duchenne).

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.