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EMA Product

Jevtana

Product approved by European Medicines Agency (EU)

Basic Information

Jevtana

Regulatory Information

EMEA/H/C/002018

Authorised

March 17, 2011

January 20, 2011

24

September 3, 2024

Company Information

France

82 Avenue Raspail 94250 Gentilly

SANOFI WINTHROP INDUSTRIE

Active Substances Detail

Detailed Information

Therapeutic Indication

### Therapeutic indication Jevtana in combination with prednisone or prednisolone is indicated for the treatment of patients with hormone-refractory metastatic prostate cancer previously treated with a docetaxel-containing regimen.

Overview Summary

This is a summary of the European public assessment report (EPAR) for Jevtana. 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 Jevtana.

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