drugset / Trial / NCT00803374

Combination of Anti-CD137 & Ipilimumab in Patients With Melanoma

NCT00803374

Phase 1 Withdrawn Bristol-Myers Squibb
Non-randomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to determine if BMS-663513 administered in combination with ipilimumab to patients with advanced malignant melanoma is safe and tolerable

Timeline

Start
2010-11
Primary completion
2012-07
Completion
2013-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Urelumab Monoclonal antibody 0.1 mg/kg Intravenous
Subject Urelumab Monoclonal antibody 0.3 mg/kg Intravenous
Subject Urelumab Monoclonal antibody 1 mg/kg Intravenous
Subject Urelumab Monoclonal antibody 3 mg/kg Intravenous
Subject Urelumab Monoclonal antibody 10 mg/kg Intravenous
Background Ipilimumab Monoclonal antibody 10 mg/kg Intravenous

Indications