drugset / Trial / NCT02905266

A Safety and Efficacy Study of Multiple Administration Regimens for Nivolumab Plus Ipilimumab in Subjects With Melanoma

NCT02905266

Phase 3 Completed 106 enrolled Bristol-Myers Squibb
RandomizedParallel-groupOpen-labelTreatment

Summary

This is a safety and efficacy study of different administration regimens of nivolumab plus Ipilimumab in subjects with previously untreated, unresectable or metastatic melanoma.

Timeline

Start
2016-10-27
Primary completion
2017-10-23
Completion
2019-10-25

Drugs

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

Indications