This study will determine the safety of intravenous and oral doses of ddi administered on a b.i.d. regimen to patients with AIDS or ARC. It will establish the maximum tolerated dose and pharmacokinetic parameters for ddi. Preliminary data on effects of ddi on HIV replication, p24 antigen levels and AIDS-associated immunologic parameters will be obtained.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
General Clinical Research Centers Program (M01)
Project #
2M01RR000096-30A1
Application #
3863969
Study Section
Project Start
Project End
Budget Start
Budget End
Support Year
30
Fiscal Year
1991
Total Cost
Indirect Cost
Name
New York University
Department
Type
DUNS #
004514360
City
New York
State
NY
Country
United States
Zip Code
10012
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