Page contentsPage contents Key facts Decision Key facts Active substance Enfortumab vedotin Therapeutic area Oncology Decision number P/0114/2018 PIP number EMEA-002299-PIP01-17 Pharmaceutical form(s) Powder for concentrate for solution for infusion Condition(s) / indication(s) Treatment of urothelial carcinoma Route(s) of administration Intravenous use Contact for public enquiries Astellas Pharma Europe B.V.Tel. +31 7154 55878E-mail: contact.nl@astellas.com Decision type W: decision granting a waiver in all age groups for all conditions or indications Decision date 11/04/2018 Compliance check done No Decision P/0114/2018: EMA decision of 11 April 2018 on the granting of a product specific waiver for enfortumab vedotin (EMEA-002299-PIP01-17)Adopted Reference Number: EMA/152182/2018 Corr. English (EN) (166.9 KB - PDF)First published: 25/07/2018 Last updated: 06/05/2026 View Share this page