drugset / Trial / NCT00162123

A Companion Study for Patients Enrolled in Prior/Parent Ipilimumab Studies

NCT00162123 ↗

Phase 2 Completed 248 enrolled Bristol-Myers Squibb
Non-randomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study was to evaluate the continued use of ipilimumab in patients who had reinduction at the time of disease progression or to continue maintenance treatment. In addition, this study will continue to follow patients who have taken ipilimumab, but who are not eligible for maintenance or reinduction therapy.

Timeline

Start
2006-05
Primary completion
2012-09
Completion
2014-04

Drugs

EvaluationDrugModalityDoseRoute
Subject Ipilimumab Monoclonal antibody 0.3 mg/kg Intravenous
Subject Ipilimumab Monoclonal antibody 3 mg/kg Intravenous
Subject Ipilimumab Monoclonal antibody 10 mg/kg Intravenous

Indications