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Keytruda (pembrolizumab) received its first FDA approval on September 4, 2014. [1]
The initial FDA approval was for patients with unresectable or metastatic melanoma that had progressed after treatment with ipilimumab (and, if BRAF V600 mutation–positive, a BRAF inhibitor). [1]
After its first approval in 2014, Keytruda’s FDA label expanded across additional tumor types and settings over subsequent years (including different lines of therapy and combinations). [1] Sources: [1] https://www.drugs.com/history/keytruda.html
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