FDA approves new indication for AstraZeneca's Iressa, and companion diagnostic
The US Food and Drug Administration yesterday approved Anglo-Swedish pharma major AstraZeneca’s (LSE: AZN) Iressa (gefitinib) for the first-line treatment of patients with metastatic non-small cell lung cancer (NSCLC) whose tumors harbor specific types of epidermal growth factor receptor (EGFR) gene mutations, as detected by an FDA-approved test.
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