EU approves Merck Keytruda-paclitaxel regimen for PD-L1+ platinum-resistant ovarian cancer

Reuters04-02

European Commission cleared Keytruda with paclitaxel, with or without bevacizumab, for adults with PD-L1 CPS ≥1 platinum-resistant recurrent ovarian, fallopian tube, or primary peritoneal cancer.
Label covers patients who received 1-2 prior systemic regimens.
Decision based on Phase 3 KEYNOTE-B96 data showing improved progression-free survival, hazard ratio 0.72.
Trial also met overall survival endpoint, hazard ratio 0.76.

Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Merck & Co. Inc. published the original content used to generate this news brief via Business Wire (Ref. ID: 20260402989361) on April 02, 2026, and is solely responsible for the information contained therein.

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