The purpose of this study is to determine the response rate and duration of response to topotecan administered as a continuous infusion for 72 hrs. every 7 days in patients with platinum resistant ovarian cancer. Further objectives are to (1) describe the toxicity associated with this regimen and (2) determine topotecan pharmacokinetic parameters. At this time, the two-stage plan for patient accrual is in stage 2. Thirty-one subjects have been screened and 10 enrolled. Accrual will continue. No preliminary statistical analysis has been done.

Project Start
1998-12-01
Project End
1999-11-30
Budget Start
1998-10-01
Budget End
1999-09-30
Support Year
37
Fiscal Year
1999
Total Cost
Indirect Cost
Name
Case Western Reserve University
Department
Type
DUNS #
077758407
City
Cleveland
State
OH
Country
United States
Zip Code
44106
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