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The FDA has approved Merck & Co Inc’s (NYSE: MRK) Keytruda, an anti-PD-1 therapy, for the adjuvant treatment of renal cell carcinoma (RCC). The news comes almost half a year after Merck took the stage at ASCO to report Phase 3 data showing Keytruda cut the risk of cancer relapse or death by 32% compared to placebo, hitting the primary endpoint of disease-free survival.
...read full article on Benzinga
