drugset / Trial / NCT02247349

BMS-986012 in Relapsed/Refractory SCLC

NCT02247349

Phase 1/2 Completed 106 enrolled Bristol-Myers Squibb
Non-randomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to determine the safety, tolerability, pharmacokinetics, immunogenicity, antitumor activity and pharmacodynamics of BMS-986012 alone and in combination with nivolumab in patients with relapsed/refractory SCLC.

Timeline

Start
2014-11-14
Primary completion
2022-12-21
Completion
2022-12-22

Drugs

EvaluationDrugModalityDoseRoute
Subject Nivolumab Monoclonal antibody
Subject atigotatug Monoclonal antibody Intravenous