Specific aims of this study are to assess the safety of rhEndostatin adminstered intravenously once daily for 28 days over a range of potentially therapeutic doses by evaluation of the frequency, severity and duration of treatment-emergent adverse experiences in patients with specific types of cancer that are measurable and refractory to existing treatment. Also, to determine the serum pharmacokinetics of rhEndostatin following the initial intravenous dose of rhEndostatin at steady state.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
General Clinical Research Centers Program (M01)
Project #
2M01RR001032-25
Application #
6407214
Study Section
National Center for Research Resources Initial Review Group (RIRG)
Project Start
1977-12-01
Project End
2004-11-30
Budget Start
Budget End
Support Year
25
Fiscal Year
2000
Total Cost
Indirect Cost
Name
Beth Israel Deaconess Medical Center
Department
Type
DUNS #
076593722
City
Boston
State
MA
Country
United States
Zip Code
02215
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