The purpose of this study is to compare the efficacy of two doses of oral ddI, determined by overall survival, changes in neurologic and neuropsychological functioning, and growth status. It will also evaluate the safety and tolerance of the two doses as determined by the following parameters: pancreatic, muscular, hepatic, and neurologic toxicity.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
General Clinical Research Centers Program (M01)
Project #
2M01RR002558-08A1
Application #
3788657
Study Section
Project Start
Project End
Budget Start
Budget End
Support Year
8
Fiscal Year
1993
Total Cost
Indirect Cost
City
Houston
State
TX
Country
United States
Zip Code
77225
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