drugset / Trial / NCT01714739

A Study of an Anti-KIR Antibody Lirilumab in Combination With an Anti-PD1 Antibody Nivolumab and Nivolumab Plus an Anti-CTLA-4 Ipilimumab Antibody in Patients With Advanced Solid Tumors

NCT01714739

Phase 1/2 Completed 337 enrolled Bristol-Myers Squibb
RandomizedParallel-groupTriple-blindTreatment

Summary

To assess the safety and tolerability and preliminary anti-tumor activity of lirilumab (BMS-986015) given in combination with nivolumab (BMS-936558) and to identify dose limiting toxicities (DLTs) and the maximally tolerated dose (MTD) of the combination. In addition, to assess the combinations of lirilumab and nivolumab or lirilumab and nivolumab plus ipilimumab (BMS-734016) in subjects with advanced (metastatic and/or unresectable) refractory solid tumors.

Timeline

Start
2012-10-07
Primary completion
2019-12-13
Completion
2019-12-13

Drugs

EvaluationDrugModalityDoseRoute
Subject Ipilimumab Monoclonal antibody
Subject Lirilumab Monoclonal antibody
Subject Nivolumab Monoclonal antibody