drugset / Trial / NCT00516451

Phase I Study of BMS-690514 in Japanese Patients With Solid Tumors

NCT00516451

Phase 1 Completed 9 enrolled Bristol-Myers Squibb
Non-randomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this clinical study is to identify the maximum tolerated dose (MTD) of BMS-690514 once daily orally in Japanese subjects with advanced or metastatic solid tumors.

Timeline

Start
2007-11
Primary completion
2008-07
Completion
2008-07

Drugs

EvaluationDrugModalityDoseRoute
Subject BMS-690514 Small molecule 100 mg Oral
Subject BMS-690514 Small molecule 200 mg Oral
Subject BMS-690514 Small molecule 250 mg Oral
Subject BMS-690514 Small molecule 300 mg Oral

Indications