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EMA Product

Lysodren

Product approved by European Medicines Agency (EU)

Basic Information

Lysodren

Regulatory Information

EMEA/H/C/000521

Authorised

April 28, 2004

23

August 21, 2024

Company Information

France

25 Boulevard Romain Rolland 92120 Montrouge

ESTEVE RD FRANCE SAS

Active Substances Detail

Detailed Information

Therapeutic Indication

### Therapeutic indication Symptomatic treatment of advanced (unresectable, metastatic or relapsed) adrenal cortical carcinoma. The effect of Lysodren on non-functional adrenal cortical carcinoma is not established.

Overview Summary

This is a summary of the European public assessment report (EPAR) for Lysodren. It explains how the Committee for Medicinal Products for Human Use (CHMP) assessed the medicine to reach its opinion in favour of granting a marketing authorisation and its recommendations on the conditions of use for Lysodren.

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