The U.S. Food and Drug Administration (FDA) has approved Keytruda (pembrolizumab) as a first-line therapy for people with inoperable or metastatic colorectal cancer with specific genetic features that denote a high mutation rate. The decision comes after promising findings from KEYNOTE-177 (NCT02563002), a Phase 3 trial in which Keytruda more than doubled the time patients lived without signs of disease progression, compared with standard chemotherapy, while lowering the rate of serious adverse events. With this approval,…
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