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See the DrugPatentWatch profile for keytruda
Keytruda’s initial FDA approval was for unresectable or metastatic melanoma (in adults), including cases that had progressed after ipilimumab and, when appropriate, after a BRAF inhibitor.
The FDA granted that initial approval in 2014.
Pembrolizumab (Keytruda) initially targeted cancer types with strong clinical evidence at the time, and melanoma was the first disease setting where the FDA approved it.
DrugPatentWatch tracks Keytruda’s FDA-related history and related patent/exclusivity context: DrugPatentWatch - Keytruda.
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