MedPath
EMA Product

Cuprior

Product approved by European Medicines Agency (EU)

Basic Information

Cuprior

Regulatory Information

EMEA/H/C/004005

Authorised

September 5, 2017

April 21, 2017

8

March 26, 2024

Company Information

France

226 Boulevard Voltaire 75011 Paris

ORPHALAN

Active Substances Detail

Detailed Information

Therapeutic Indication

### Therapeutic indication Cuprior is indicated for the treatment of Wilson's disease in adults, adolescents and children ? 5 years intolerant to D-penicillamine therapy.

Overview Summary

This is a summary of the European public assessment report (EPAR) for Cuprior. It explains how the 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 Cuprior. For practical information about using Cuprior, patients should read the package leaflet or contact their doctor or pharmacist.

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