AstraZeneca has submitted market authorization application to the European Medicines Agency for oral anticancer drug, gefitinib, as a treatment for locally advanced or metastatic non-small cell lung cancer in patients who have been pre-treated with platinum-containing chemotherapy.
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The application is based on data from the Phase III Interest study, which showed that patients with pre-treated advanced non-small cell lung cancer (NSCLC) who received gefitinib had non-inferior overall survival to those treated with intravenous chemotherapy (docetaxel).
AstraZeneca said that gefitinib had a more favorable tolerability profile than docetaxel and significantly more patients receiving gefitinib had an improvement in quality of life.
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