Page contentsKey factsDecisionRelated contentRelated informationKey facts Invented name AdcetrisAdcetris Active Substance Brentuximab vedotin Therapeutic area Oncology Decision number P/0168/2015 PIP number EMEA-000980-PIP02-15 Pharmaceutical form(s) Powder for concentrate for solution for infusion Condition(s) / indication(s) Treatment of Cutaneous T-Cell Lymphoma Route(s) of administration Intravenous use Contact for public enquiries Takeda Pharma A/SUnited KingdomEmail: bharti.navsariwala@takeda.comTel.: +44 (0) 2031 168000 Decision type W: decision granting a waiver in all age groups for all conditions or indications Decision date 07/08/2015DecisionP/0168/2015: EMA decision of 7 August 2015 on the granting of a product-specific waiver for brentuximab vedotin (Adcetris), (EMEA-000980-PIP02-15)AdoptedReference Number: EMA/473694/2015 English (EN) (94.28 KB - PDF)First published: 22/09/2015Last updated: 22/09/2015ViewRelated contentAdcetris Related information Public summary of the evaluation of a proposed product-specific waiver: Brentuximab vedotin for treatment of Cutaneous T-Cell LymphomaReference Number: EMA/702731/2015Summary: Public summary of the evaluation of a proposed paediatric investigation plan. English (EN) (78.06 KB - PDF)First published: 17/12/2015Last updated: 17/12/2015ViewShare this page