drugset / Trial / NCT01413906

Phase 1 Multiple Ascending Dose Study of BMS-833923 (XL139) in Subjects With Solid Tumors

NCT01413906

Phase 1 Completed 12 enrolled Bristol-Myers Squibb
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate the tolerability and safety profile of BMS-833923 (XL139) when orally administered on a once daily schedule.

Timeline

Start
2011-11
Primary completion
2012-11
Completion
2012-11

Drugs

EvaluationDrugModalityDoseRoute
Subject BMS-833923 Small molecule 150 mg Oral
Subject BMS-833923 Small molecule 300 mg Oral
Subject BMS-833923 Small molecule 450 mg Oral

Indications