drugset / Trial / NCT01578499

A Phase 3 Trial of Brentuximab Vedotin(SGN-35) Versus Physician's Choice (Methotrexate or Bexarotene) in Participants With CD30-Positive Cutaneous T-Cell Lymphoma (ALCANZA Study)

NCT01578499

RandomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to determine objective response rate (ORR), lasting at least 4 months (ORR4), with brentuximab vedotin in participants with cluster of differentiation antigen 30 positive (CD30+) cutaneous T-cell lymphoma \[mycosis fungoides (MF) and primary cutaneous anaplastic large cell lymphoma (pcALCL) \]compared to that achieved with therapy in the control arm.

Timeline

Start
2012-06-11
Primary completion
2016-05-31
Completion
2018-07-06

Publications

Drugs

EvaluationDrugModalityDoseRoute
Comparator Bexarotene Small molecule 300 mg/m2 Oral
Subject Brentuximab Vedotin Monoclonal antibody 1.8 mg/kg Intravenous
Comparator Methotrexate Small molecule 5 mg Oral
Comparator Methotrexate Small molecule 50 mg Oral