Page contents Key factsDecisionRelated medicine informationKey facts Invented name Padcev Active Substance Enfortumab vedotin Therapeutic area Oncology Decision number P/0385/2023 PIP number EMEA-002299-PIP02-23 Pharmaceutical form(s) Powder for concentrate for solution for infusion Condition(s) / indication(s) Treatment of head and neck epithelial malignant neoplasms Route(s) of administration Intravenous use Contact for public enquiries Astellas Pharma Europe B.V.E-mail: regulatory.eu@astellas.comTel: +31 715454006 Decision type W: decision granting a waiver in all age groups for all conditions or indications Decision date 07/09/2023DecisionP/0385/2023 : EMA decision of 7 September 2023 on the granting of a product specific waiver for enfortumab vedotin (Padcev), (EMEA-002299-PIP02-23)Reference Number: EMA/389081/2023 English (EN) (202.2 KB - PDF)First published: 19/09/2024ViewRelated medicine informationPadcevShare this page