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Keytruda’s first FDA approval was for melanoma. It was initially approved for patients with unresectable or metastatic melanoma with a BRAF V600 wild-type tumor and disease progression following prior therapies, based on early clinical data. [1]
The FDA first approved Keytruda in 2014. [1]
After melanoma, Keytruda expanded to multiple other indications (including several cancers with different biomarkers and treatment settings), but melanoma was the first cancer type to receive FDA approval. [1]
[1] https://www.fda.gov/drugs/drug-approvals-and-databases/drug-trials-snapshots-pembrolizumab-keytruda
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