Phase II Study of Dasatinib (BMS-354825) for Androgen-deprived Progressive Prostate Cancer
Completed · Phase 2
Conditions studied: Prostate Cancer
In brief
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.
Key facts
- Study ID
- NCT00385580
- Run by
- Bristol-Myers Squibb
- People needed
- 94
- Starts
- 2007-01-01
- Expected to finish
- 2010-10-01
- Last updated by the study team
- 2013-04-30
Who can join
Age: 18 and older. Sex: male. Healthy volunteers: not accepted.
You may qualify if…
- males, 18 or older
- proven advanced prostate cancer
- documented metastatic disease
- rising PSA levels
- castrate levels of testosterone
You may not qualify if…
- symptomatic CNS (brain or spinal cord) metastasis
- medical condition which may increase the risk of toxicity
- any prior or ongoing anti-cancer medical therapy or immunotherapy for prostate cancer other than primary androgen deprivation agents
- unable to take oral medication
Where it is running
- Cedars Sinai Medical Center — Los Angeles, California, United States
- University Of Chicago — Chicago, Illinois, United States
- The Bunting Blaustein Cancer Research Building — Baltimore, Maryland, United States
- Memorial Sloan-Kettering Cancer Center-Sidney Kimmel Center — New York, New York, United States
- Fox Chase Cancer Center — Philadelphia, Pennsylvania, United States
- Seattle Cancer Care Alliance — Seattle, Washington, United States
- University Of Wisconsin Paul P Carbone Comprehensive Ca Ctr — Madison, Wisconsin, United States
- Local Institution — Montpellier, France
- Local Institution — Paris, France
- Local Institution — Villejuif, France
- Local Institution — Rome, Italy
Full record on ClinicalTrials.gov
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