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EMA Product

Foscan

Product approved by European Medicines Agency (EU)

Basic Information

Foscan

Regulatory Information

EMEA/H/C/000318

Authorised

October 24, 2001

18

April 18, 2016

Company Information

Germany

Otto-Schott-Str. 15 07745 Jena

biolitec Pharma Ltd.

Active Substances Detail

Detailed Information

Therapeutic Indication

### Therapeutic indication Foscan is indicated for the palliative treatment of patients with advanced head and neck squamous cell carcinoma failing prior therapies and unsuitable for radiotherapy, surgery or systemic chemotherapy.

Overview Summary

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

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