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FDA approves pembrolizumab (Keytruda) for first-line treatment of MSI-H/dMMR colorectal cancer

27 Jul 2020 9:47 AM | Nathan Strunk (Administrator)

The U.S. Food and Drug Administration approved pembrolizumab (KEYTRUDA, Merck & Co.) for the first-line treatment of patients with unresectable or metastatic microsatellite instability-high (MSI-H) or mismatch repair deficient (dMMR) colorectal cancer. Read full press release.

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