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EMA Product

Nexavar

Product approved by European Medicines Agency (EU)

Basic Information

Nexavar

Regulatory Information

EMEA/H/C/000690

Authorised

July 19, 2006

35

June 7, 2024

Company Information

Germany

Kaiser-Wilhelm-Allee 1 51373 Leverkusen

BAYER AG

Active Substances Detail

Detailed Information

Therapeutic Indication

### Therapeutic indication **Hepatocellular carcinoma** Nexavar is indicated for the treatment of hepatocellular carcinoma. **Renal cell carcinoma** Nexavar is indicated for the treatment of patients with advanced renal cell carcinoma who have failed prior interferon-alpha or interleukin-2 based therapy or are considered unsuitable for such therapy. **Differentiated thyroid carcinoma** Nexavar is indicated for the treatment of patients with progressive, locally advanced or metastatic, differentiated (papillary/follicular/Hürthle cell) thyroid carcinoma, refractory to radioactive iodine.

Overview Summary

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

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