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EMA Product

Iressa

Product approved by European Medicines Agency (EU)

Basic Information

Iressa

Regulatory Information

EMEA/H/C/001016

Authorised

June 24, 2009

16

July 17, 2023

Company Information

Sweden

151 85 Södertälje

ASTRAZENECA AB

Active Substances Detail

Detailed Information

Therapeutic Indication

### Therapeutic indication Iressa is indicated for the treatment of adult patients with locally advanced or metastatic non-small-cell lung cancer with activating mutations of epidermal-growth-factor-receptor tyrosine kinase.

Overview Summary

This is a summary of the European public assessment report (EPAR). It explains how the Committee for Medicinal Products for Human Use (CHMP) assessed the studies performed, to reach their recommendations on how to use the medicine. If you need more information about your medical condition or your treatment, read the package leaflet (also part of the EPAR) or contact your doctor or pharmacist. If you want more information on the basis of the CHMP recommendations, read the scientific discussion (also part of the EPAR).

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