EU approves Merck Keytruda plus Padcev for cisplatin-ineligible resectable muscle-invasive bladder cancer

Merck & Co., Inc.

Merck & Co., Inc.

MRK

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  • EU cleared Merck’s Keytruda with Padcev for perioperative use in cisplatin-ineligible, resectable muscle-invasive bladder cancer.
  • Phase 3 KEYNOTE-905 showed a 60% cut in event-free survival events, a 50% reduction in deaths versus surgery alone.
  • Approval covers all 27 EU states, Iceland, Liechtenstein, Norway; rollout depends on country reimbursement decisions.


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: 202606240645BIZWIRE_USPR_____20260624_BW345655) on June 24, 2026, and is solely responsible for the information contained therein.

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