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

Outcome

Met primary endpoint

registry analysis (superiority test); A+AVD vs ABVD; p = 0.035; Hazard Ratio (HR) 0.770 (95% CI 0.603 to 0.983); Log Rank NCT01712490 ↗

paper The primary analysis showed improved modified progression-free survival with A+AVD. PMID 34048680 ↗

release “ECHELON-1 clinical trial met its primary endpoint” takeda.com ↗

release “Topline data were reported in June 2017 demonstrating the ECHELON-1 trial met its primary endpoint of a statistically significant improvement in modified progression-free survival” takeda.com ↗

release “ECHELON-1 trial demonstrated that the ADCETRIS plus AVD arm showed a statistically significant improvement in modified progression free survival” takeda.com ↗

release “ECHELON-1 trial achieved its primary endpoint” takeda.com ↗

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