The purpose of this research is to determine the effectiveness of CGC-11047 in subjects with metastatic hormone refractory prostate cancer as measured by changes in PSA.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
23
CGC-11047 IV weekly for 3 weeks followed by one rest week (4weeks=1cycle)
University of Wisconsin Hospital and Clinics
Madison, Wisconsin, United States
Efficacy
Time frame: 8 weeks
Safety
Time frame: Throughout and for 28 days post drug
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