This is a phase III randomized clinical trial of SU101, an inhibitor of platelet-derived growth factor signaling, versus oral procarbazine for recurrent glioblastoma multiforme of the brain. The study is sponsored by the Sugen Corporation. SU101 has shown activity in Phase I and I/II trials, and the maximum tolerated dose and major toxicities have been determined. Oral procarbazine is a standard chemotherapy treatment for recurrent glioblastoma. The primary is survival. Sugen plans to enroll 380 patients nationally. We project enrollment of 24 patients over 2 years at UMMC. Patients randomized to SU101 will receive 6-hour infusions in the GCRC outpatient setting on 10 occasions during the first 8-week cycle and 7 occasions during subsequent cycles. These patients will also need blood drawn in the GCRC 4 times during each cycle and sent to a reference lab. Patients randomized to procarbazine will need only the blood draws.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
General Clinical Research Centers Program (M01)
Project #
3M01RR000042-39S1
Application #
6263699
Study Section
Project Start
1998-12-01
Project End
1999-11-30
Budget Start
1998-10-01
Budget End
1999-09-30
Support Year
39
Fiscal Year
1999
Total Cost
Indirect Cost
Name
University of Michigan Ann Arbor
Department
Type
DUNS #
791277940
City
Ann Arbor
State
MI
Country
United States
Zip Code
48109
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