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News 2026-06-25 10:45 UTC

MRK: FDA Approves KEYTRUDA

MRK's KEYTRUDA and KEYTRUDA QLEX are approved by the FDA for first-line treatment of PD-L1+ advanced triple-negative breast cancer

News 2026-06-24 10:53 UTC

MRK: Approves KEYTRUDA

European Commission approves KEYTRUDA plus Padcev for adults with cisplatin-ineligible resectable muscle-invasive bladder cancer

News 2026-06-24 10:52 UTC

MRK: EU Approves Keytruda

The European Union approves Merck's Keytruda in combination with Padcev for adults with resectable muscle-invasive bladder cancer

News 2026-06-24 10:45 UTC

MRK Gets EU Approval

MRK's KEYTRUDA and Padcev approved by European Commission for treatment of muscle-invasive bladder cancer