drugset / Trial / NCT00644488

A Phase I Study of BMS-641988 in Japanese Patients With Castration Resistant Prostate Cancer

NCT00644488 ↗

Phase 1 Completed 7 enrolled Bristol-Myers Squibb
Non-randomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this clinical study is to assess the safety and tolerability of BMS-641988 once daily orally in Japanese patients with castration resistant prostate cancer

Timeline

Start
2008-07
Primary completion
2009-03
Completion
2009-03

Drugs

EvaluationDrugModalityDoseRoute
Subject BMS-641988 Unknown 20 mg Oral
Subject BMS-641988 Unknown 40 mg Oral
Subject BMS-641988 Unknown 60 mg Oral
Subject BMS-641988 Unknown 100 mg Oral

Indications