AstraZeneca's Iressa under FDA review for 2nd US chance
This article was originally published in Scrip
The FDA accepted for review AstraZeneca's new drug application (NDA) for Iressa (gefitinib) as a targeted monotherapy for the first-line treatment of patients with advanced or metastatic epidermal growth factor receptor mutation positive (EGFRm) non-small cell lung cancer (NSCLC), as identified through a companion diagnostic test.
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