This is an open-label, non-randomized, Phase I dose-escalating study of rhIL-12 administered by intraperitoneal (IP) infusion in adult male or female patients with measurable disseminated intraperitoneal cancer that is residual, recurrent or metastatic. Neither a control or placebo group will be utilized. The primary objectives are to assess the safety, mnaximum tolerated lose and therapeutic effect of IPIL-12 given by 3 hour infusion in patients with platinum refractory small volume intraperitoneal ovarian cancer. To test whether IPIL-12 can be given on an outpatient basis with sufficient support for management of side effects and sympton. Attempt to quantitate the immunopharmacology and biological impact of IPIL-12 on peripheral blood and peritoneal immunocyte populations by both markers of immune activation as well as ovarian cancer specific T-cell responses and natural killer cell activity.

Project Start
1999-12-01
Project End
2000-11-30
Budget Start
1998-10-01
Budget End
1999-09-30
Support Year
39
Fiscal Year
2000
Total Cost
$3,034
Indirect Cost
Name
University of Pittsburgh
Department
Type
DUNS #
053785812
City
Pittsburgh
State
PA
Country
United States
Zip Code
15213
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