drugset / Trial / NCT00385580

Phase II Study of Dasatinib (BMS-354825) for Androgen-deprived Progressive Prostate Cancer

NCT00385580 ↗

Phase 2 Completed 94 enrolled Bristol-Myers Squibb
Non-randomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to learn if men with metastatic prostate cancer and rising Prostate Specific Antigen (PSA), who have been surgically castrated or are undergoing androgen deprivation with Luteinizing Hormone Releasing Hormone (LHRH) treatment, respond to dasatinib. The safety of this treatment will also be studied.

Timeline

Start
2007-01
Primary completion
2008-12
Completion
2010-10

Drugs

EvaluationDrugModalityDoseRoute
Subject dasatinib anhydrous Small molecule 70 mg Oral
Subject dasatinib anhydrous Small molecule 100 mg Oral

Indications