drugset / Trial / NCT02005471

A Study to Evaluate the Benefit of Venetoclax Plus Rituximab Compared With Bendamustine Plus Rituximab in Participants With Relapsed or Refractory Chronic Lymphocytic Leukemia (CLL)

NCT02005471 ↗

Phase 3 Completed 389 enrolled Hoffmann-La Roche AbbVie · collab
RandomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this open-label, multicenter, randomized, Phase III study is to evaluate the benefit of venetoclax in combination with rituximab compared with bendamustine in combination with rituximab in participants with relapsed or refractory CLL. Participants will be randomly assigned in 1:1 ratio to receive either venetoclax + rituximab (Arm A) or bendamustine + rituximab (Arm B).

Timeline

Start
2014-03-17
Primary completion
2017-05-08
Completion
2022-08-03

Outcome

Met primary endpoint

paper the rate of investigator-assessed progression-free survival was significantly higher in the venetoclax-rituximab group PMID 29562156 ↗

paper P<0.001 by the stratified log-rank test PMID 29562156 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Comparator Bendamustine Small molecule 70 mg/m2 Intravenous
Subject Venetoclax Small molecule 400 mg Oral
Background Rituximab Monoclonal antibody 500 mg/m2 Intravenous