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EMA Product

Erivedge

Product approved by European Medicines Agency (EU)

Basic Information

Erivedge

Regulatory Information

EMEA/H/C/002602

Authorised

July 12, 2013

April 25, 2013

15

March 20, 2023

Company Information

Germany

Emil-Barell-Strasse 1 79639 Grenzach-Wyhlen

Roche Registration GmbH

Active Substances Detail

Detailed Information

Therapeutic Indication

### Therapeutic indication Erivedge is indicated for the treatment of adult patients with: \- symptomatic metastatic basal cell carcinoma \- locally advanced basal cell carcinoma inappropriate for surgery or radiotherapy

Overview Summary

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

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