This is a phase II study to determine the response to suramin of previously untreated metastatic melanoma, and to evaluate the safety and toxicity of this agent. It is anticipated that 29 patients will enter this single center study. Suramin will be infused via a peripheral vein or permanent central venous access device. The initial dose will be infused over 2 hours; all subsequent doses will be administered over one hour. All patients will have a 12 week break between cycle #1 and cycle #2.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
General Clinical Research Centers Program (M01)
Project #
3M01RR000056-38S3
Application #
6219249
Study Section
Project Start
1998-12-01
Project End
1999-11-30
Budget Start
1998-10-01
Budget End
1999-09-30
Support Year
38
Fiscal Year
1999
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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