drugset / Trial / NCT02420821

A Study of Atezolizumab in Combination With Bevacizumab Versus Sunitinib in Participants With Untreated Advanced Renal Cell Carcinoma (RCC)

NCT02420821 ↗

Phase 3 Completed 915 enrolled Hoffmann-La Roche
RandomizedParallel-groupOpen-labelTreatment

Summary

This multi-center, randomized, open-label study will evaluate the efficacy and safety of atezolizumab plus bevacizumab versus sunitinib in participants with inoperable, locally advanced, or metastatic RCC who have not received prior systemic active or experimental therapy, either in the adjuvant or metastatic setting.

Timeline

Start
2015-05-20
Primary completion
2020-02-14
Completion
2021-12-13

Outcome

Mixed primary results

registry MEDIAN Sunitinib: 7.5 (6.8 to 9.7) months NCT02420821 ↗

registry MEDIAN Atezolizumab + Bevacizumab: 11.2 (8.6 to 14.3) months NCT02420821 ↗

registry analysis (superiority test); Sunitinib vs Atezolizumab + Bevacizumab; p = 0.0205; Hazard Ratio (HR) 0.73 (95% CI 0.57 to 0.95); Log Rank NCT02420821 ↗

registry analysis (superiority test); Sunitinib vs Atezolizumab + Bevacizumab; p = 0.2675; Hazard Ratio (HR) 0.91 (95% CI 0.76 to 1.08); Log Rank NCT02420821 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Atezolizumab Monoclonal antibody 1200 mg Intravenous
Subject Bevacizumab Monoclonal antibody 15 mg/kg Intravenous
Comparator Sunitinib Small molecule 50 mg Oral

Indications