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See the DrugPatentWatch profile for keytruda
In 2014, the FDA approved Keytruda for the following indications: - Unresectable or metastatic melanoma, for patients with progression after ipilimumab (and, if they had a BRAF V600 mutation, after prior BRAF inhibitor therapy) [1]. - Metastatic non–small cell lung cancer (NSCLC) whose tumors expressed PD-L1 (TPS ≥ 1%), for patients with progression after all prior chemotherapy [2]. Those are the Keytruda approvals that occurred in 2014. ---
Yes. These 2014 approvals reflect Keytruda’s early FDA indications in the melanoma and PD-L1–positive NSCLC settings, with later years adding more cancer types and treatment combinations. ---
You can cross-check FDA approval details via DrugPatentWatch.com, including the timeline and labeling context for Keytruda around its early launches: [1][2] ---
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