drugset / Trial / NCT00339144

Study of Dasatinib (BMS-354825) in Patients With Solid Tumors

NCT00339144

Phase 1 Completed 16 enrolled Bristol-Myers Squibb
Non-randomizedParallel-groupOpen-labelTreatment

Summary

The primary objective of this study is to determine the maximum tolerated dose (MTD) or the maximum administered dose (MAD) of Dasatinib (BMS-354825) in patients in Japan.

Timeline

Start
2007-01
Primary completion
2008-09
Completion
2008-09

Drugs

EvaluationDrugModalityDoseRoute
Subject dasatinib anhydrous Small molecule 100 mg Oral
Subject dasatinib anhydrous Small molecule 150 mg Oral
Subject dasatinib anhydrous Small molecule 200 mg Oral

Indications