drugset / Trial / NCT01569295

Study Evaluating the Efficacy and Safety of Idelalisib in Combination With Bendamustine and Rituximab for Previously Treated Chronic Lymphocytic Leukemia (CLL) (Tugela )

NCT01569295 ↗

Phase 3 Completed 416 enrolled Gilead Sciences
RandomizedParallel-groupTriple-blindTreatment

Summary

The primary objective of this study is to evaluate the effect of the addition of idelalisib (formerly GS-1101) to bendamustine + rituximab (BR) on progression-free survival (PFS) in participants with previously treated chronic lymphocytic leukemia (CLL)

Timeline

Start
2012-06-15
Primary completion
2019-06-10
Completion
2019-06-10

Outcome

Met primary endpoint

registry analysis (superiority test); Idelalisib + Bendamustine + Rituximab vs Placebo + Bendamustine + Rituximab; p < 0.0001; Hazard Ratio (HR) 0.35 (95% CI 0.27 to 0.45) NCT01569295 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Idelalisib Small molecule 150 mg Oral
Background Bendamustine Small molecule 70 mg/m2 Intravenous
Background Rituximab Monoclonal antibody 500 mg/m2 Intravenous