drugset / Trial / NCT02253992

An Investigational Immuno-therapy Study to Determine the Safety of Urelumab Given in Combination With Nivolumab in Solid Tumors and B-cell Non-Hodgkin's Lymphoma

NCT02253992

Phase 1/2 Terminated 232 enrolled Bristol-Myers Squibb
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to determine which doses of Urelumab and Nivolumab are safe and tolerable when they are given together.

Timeline

Start
2014-09-29
Primary completion
2019-05-24
Completion
2019-05-24

Drugs

EvaluationDrugModalityDoseRoute
Subject Nivolumab Monoclonal antibody 3 mg/kg
Subject Nivolumab Monoclonal antibody 240 mg
Subject Urelumab Monoclonal antibody 3 mg
Subject Urelumab Monoclonal antibody 8 mg