This is an open label, Phase II, multicenter study. Patients will receive Atragen 140mg/m2-three times weekly. The drug will be given on Monday, Wednesday and Friday over a course of 28 days. Patients will continue to receive therapy for a minimum of six months, unless evidence of disease progression. The primary objectives of this study are to assess the efficacy of Atragen in the treatment of patients with androgen-independent, metastatic cancer of the prostate and to evaluate the safety of Atragen in this patient population.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
General Clinical Research Centers Program (M01)
Project #
5M01RR000056-41
Application #
6566471
Study Section
National Center for Research Resources Initial Review Group (RIRG)
Project Start
2001-12-01
Project End
2002-11-30
Budget Start
Budget End
Support Year
41
Fiscal Year
2002
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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