drugset / Trial / NCT00729664

Multiple Ascending Dose (MDX1105-01)

NCT00729664 ↗

Phase 1 Completed 281 enrolled Bristol-Myers Squibb
Non-randomizedParallel-groupOpen-labelTreatment

Summary

Collection of survival data, evaluation of PDL-1 expression in tumors, and evaluation of PD-L1 receptor occupancy in peripheral blood has been added.

Timeline

Start
2009-02
Primary completion
2015-07
Completion
2015-07

Drugs

EvaluationDrugModalityDoseRoute
Subject BMS-936559 Monoclonal antibody 0.1 mg/kg Intravenous
Subject BMS-936559 Monoclonal antibody 0.3 mg/kg Intravenous
Subject BMS-936559 Monoclonal antibody 1 mg/kg Intravenous
Subject BMS-936559 Monoclonal antibody 3 mg/kg Intravenous
Subject BMS-936559 Monoclonal antibody 10 mg/kg Intravenous

Indications

No indication recorded.