Post-Authorisation Safety Study (PASS) MA25101: An Observational Cohort Study of the Safety of Brentuximab Vedotin in the Treatment of Relapsed or Refractory CD30+ Hodgkin Lymphoma and Relapsed or Refractory Systemic Anaplastic Large Cell Lymphoma (ARROVEN)

First published 28/02/2013

Last updated 02/07/2024

EU PAS number:

EUPAS3583

Study

Finalised

Documents

Study protocol

Initial protocol

MA25101_Post-Authorisation Safety Study (PASS)_Amendment 2 w MPI change

English (986.79 KB - PDF)View document

Updated protocol

MA25101 Protocol Amend 4 2017-01-27

First published: 22/02/2024

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Study results

FINAL Takeda ARROVEN PASS_CSR_v3.0_27Nov2019

English (1.1 MB - PDF)View document

MA25101 - Abstract

English (693.93 KB - PDF)View document

Study report

Other information

ENCePP Seal

ENCePP Seal documents

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