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EMA Product

Procysbi

Product approved by European Medicines Agency (EU)

Basic Information

Procysbi

Regulatory Information

EMEA/H/C/002465

Authorised

September 5, 2013

June 27, 2013

16

September 22, 2023

Company Information

Italy

Via Palermo 26/A 43122 Parma

CHIESI FARMACEUTICI S.P.A.

Active Substances Detail

Detailed Information

Therapeutic Indication

### Therapeutic indication Procysbi is indicated for the treatment of proven nephropathic cystinosis. Cysteamine reduces cystine accumulation in some cells (e.g. leukocytes, muscle and liver cells) of nephropathic cystinosis patients and, when treatment is started early, it delays the development of renal failure.

Overview Summary

This is a summary of the European public assessment report (EPAR) for Procysbi. It explains how the European Medicines Agency assessed the medicine to recommend its authorisation in the EU and its conditions of use. It is not intended to provide practical advice on how to use Procysbi. For practical information about using Procysbi, patients should read the package leaflet or contact their doctor or pharmacist.

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