Oxervate

cenegermin · Dompe' Farmaceutici S.p.A.
ORPHAN AUTHORISED IN THE EU

What Oxervate is used for

Treatment of moderate (persistent epithelial defect) or severe (corneal ulcer) neurotrophic keratitis in adults

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
Oxervate
Active substance
cenegermin
Disease area
Keratitis
Medicine group
Ophthalmologicals
ATC code
S01
Marketing authorisation holder
Dompe' Farmaceutici S.p.A.
Authorised in the EU since
2017

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 Oxervate used for?

Treatment of moderate (persistent epithelial defect) or severe (corneal ulcer) neurotrophic keratitis in adults

What is the active substance in Oxervate?

Oxervate contains cenegermin.

Who makes Oxervate?

The EU marketing authorisation holder is Dompe' Farmaceutici S.p.A..

Is Oxervate an orphan medicine?

Yes. Oxervate is designated an orphan medicine in the EU, for a rare disease (Keratitis).

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.