drugset / Trial / NCT03029780

An Investigational Immuno-Therapy Safety and Efficacy Study of Multiple Administration Regimens for Nivolumab Plus Ipilimumab in Subjects With Renal Cell Carcinoma

NCT03029780 ↗

Phase 2 Completed 104 enrolled Bristol-Myers Squibb
RandomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate safety and efficacy of different administration regimens of nivolumab plus ipilimumab in subjects with renal cell carcinoma.

Timeline

Start
2017-02-16
Primary completion
2017-11-27
Completion
2021-06-15

Outcome

Results reported · no primary-endpoint met/missed verdict (typical of a dose-finding / safety study)

paper Both studies met their primary endpoint. PMID 40614118 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Ipilimumab Monoclonal antibody 1 mg/kg Other
Subject Nivolumab Monoclonal antibody 3 mg/kg Other

Indications