drugset / Trial / NCT01712490

A Frontline Therapy Trial in Participants With Advanced Classical Hodgkin Lymphoma

NCT01712490

Phase 3 Completed 1334 enrolled Takeda Seagen Inc. · collab
RandomizedParallel-groupOpen-labelTreatment

Summary

This open-label, randomized, 2-arm, multicenter, phase 3 study has the primary objective of comparing the modified progression-free survival (mPFS) obtained with brentuximab vedotin (ADCETRIS®) plus AVD (doxorubicin \[Adriamycin\], vinblastine, and dacarbazine; abbreviated A+AVD) versus that obtained with ABVD (doxorubicin \[Adriamycin\],bleomycin, vinblastine, and dacarbazine) for the frontline treatment of advanced classical Hodgkin lymphoma(HL)

Timeline

Start
2012-11-09
Primary completion
2017-04-20
Completion
2026-02-02

Publications

Drugs

EvaluationDrugModalityDoseRoute
Comparator Bleomycin Unknown 10 unknown Intravenous
Subject Brentuximab Vedotin Monoclonal antibody 1.2 mg/kg Intravenous
Background Dacarbazine Small molecule 375 mg/m2 Intravenous
Background Doxorubicin Other / unclassified 25 mg/m2 Intravenous
Background Vinblastine Small molecule 6 mg/m2 Intravenous

Indications