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FDA Grants Priority Review to Imfinzi-Enfortumab Vedotin Regimen for Muscle-Invasive Bladder Cancer

Summary by Patient Worthy
As reported on PharmaBiz, the FDA has accepted AstraZeneca’s supplemental Biologics License Application for durvalumab plus neoadjuvant enfortumab vedotin in patients with muscle-invasive bladder cancer who cannot receive or have chosen not to receive cisplatin-based chemotherapy. The US Food and Drug Administration has granted Priority Review to AstraZeneca’s supplemental Biologics License Application (sBLA) for Imfinzi […]
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Patient Worthy broke the news on Thursday, October 1, 2026.
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