Page contentsPage contents Key facts Decision Related medicine information Key facts Invented name AdcetrisAdcetris Active substance Brentuximab vedotin Therapeutic area Oncology Decision number P/0327/2018 PIP number EMEA-000980-PIP04-18 Pharmaceutical form(s) Powder for concentrate for solution for infusion Condition(s) / indication(s) Treatment of Mature T and NK neoplasms (excluding anaplastic large-cell lymphoma and cutaneous Tcell lymphoma) Route(s) of administration Intravenous use Contact for public enquiries Takeda Pharma A/S Tel. +44 2031168000E-mail: paediatrics@tgrd.com Decision type W: decision granting a waiver in all age groups for all conditions or indications Decision date 08/10/2018 Compliance check done No Decision P/0327/2018: EMA decision of 8 October 2018 on the granting of a product specific waiver for brentuximab vedotin (Adcetris), (EMEA-000980-PIP04-18)Adopted Reference Number: EMA/646757/2018 English (EN) (69.56 KB - PDF)First published: 11/01/2019 View Related medicine information Adcetris Share this page