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FDA accepts sBLA for Keytruda in high-risk stage II melanoma – Merck Inc

Written by | 13 Aug 2021

Merck Inc announced that the Phase III KEYNOTE-716 trial investigating Keytruda (pembrolizumab), Merck’s anti-PD-1 therapy, met its primary endpoint of recurrence-free survival (RFS) for the adjuvant treatment of… read more.

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