drugset / Trial / NCT00207103

MAD in Cancer Patients: Safety of BMS-582664 in Patients With Advanced or Metastatic Solid Tumors

NCT00207103

Phase 1 Completed 68 enrolled Bristol-Myers Squibb
Non-randomizedParallel-groupOpen-labelTreatment

Summary

This is a Phase I dose escalation study to determine the safety, pharmacokinetics and pharmacodynamics of BMS-582664 in patients with advanced or metastatic solid tumors.

Timeline

Start
2004-09
Primary completion
2007-10
Completion
2008-09

Drugs

EvaluationDrugModalityDoseRoute
Subject Brivanib Small molecule 180 mg Oral
Subject Brivanib Small molecule 320 mg Oral
Subject Brivanib Small molecule 600 mg Oral
Subject Brivanib Small molecule 800 mg Oral
Subject Brivanib Small molecule 1000 mg Oral