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EMA Validates Type II Variation for Padcev® (enfortumab vedotin) with Merck’s Keytruda® in for First-Line Treatment of Advanced Bladder Cancer

Jan 29, 2024

Astellas announced that on 26 January the European Medicines Agency (EMA) validated for review a Type II variation application for PADCEVTM (enfortumab vedotin) with KEYTRUDA® (pembrolizumab) as a combination therapy for the first-line treatment of adult patients with previously untreated locally advanced or metastatic urothelial cancer (la/mUC).