The primary objective of this study is to evaluate the safety and toxicity profile of LY300502 administered by four different doses and to measure the reduction in serum DHT levels from baseline in patients treated at these doses to define the maximum biological effect (MBE) dose. This is a non-randomized dose finding study of LY300502 in patients with metastatic prostate cancer who have failed or are not candidates for convention hormonal therapy. LY300502 will be administered three times daily for a period of 12 weeks. In order to define the dose at which DHT suppression is maximized with acceptable safety and pharmacokinetic profiles, patients will be entered in four cohorts of eight patients each.

Project Start
2000-12-01
Project End
2001-11-30
Budget Start
Budget End
Support Year
40
Fiscal Year
2001
Total Cost
Indirect Cost
Name
University of Pittsburgh
Department
Type
DUNS #
053785812
City
Pittsburgh
State
PA
Country
United States
Zip Code
15213
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