drugset / Trial / NCT00886782

A Study of BMS-863233 in Patients With Advanced and/or Metastatic Solid Tumors

NCT00886782 ↗

Phase 1/2 Terminated 11 enrolled Bristol-Myers Squibb Exelixis · collab
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to determine safety, tolerability and maximum tolerated dose of BMS-863233 in subjects advanced and/or Metastatic solid tumors.

Timeline

Start
2009-05-31
Primary completion
2010-08-04
Completion
2010-08-04

Drugs

EvaluationDrugModalityDoseRoute
Subject BMS-863233 Small molecule — Oral