drugset / Trial / NCT00289640

Study of Ipilimumab (MDX-010) Monotherapy in Patients With Previously Treated Unresectable Stage III or IV Melanoma

NCT00289640 ↗

Phase 2 Completed 210 enrolled Bristol-Myers Squibb Medarex · collab
RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of this clinical research study is to compare the best overall response rate (BORR)(as per modified WHO criteria) in patients with previously treated, therapy-refractory, or -intolerant, Stage III (unresectable) or Stage IV melanoma receiving ipilimumab doses of 0.3, 3, and 10 mg/kg. The safety of this product will also be evaluated.

Timeline

Start
2006-04
Primary completion
2007-07
Completion
2007-07

Outcome

Met primary endpoint

paper 0% (0.0-4.9) for 0.3 mg/kg (p=0.0015; trend test). PMID 20004617 ↗

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