The Cancer Letter

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Drugs & Targets

FDA accepts sBLA for Keytruda as single agent for MSI-H/dMMR advanced endometrial carcinoma

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FDA has accepted for review a supplemental Biologics License Application seeking approval for Keytruda as a single agent for the treatment of patients with advanced endometrial carcinoma that is microsatellite instability-high or mismatch repair deficient, who have disease progression following prior systemic therapy in any setting and are not candidates for curative surgery or radiation. 

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