To determine the maximum tolerated dose of subcutaneous IL-2, a phase I trial has been undertaken in asymptomatic HIV+ individuals. Secondary aims are to determine whether low IL-2 doses will have any effect on immune reactivity without activating virus production. Patients with a CD4+ T cell count of 200-500/mm3 and negative HIV p24 Ag will be entered in the study. Subcutaneous IL-2 will be administered on a daily basis for 6 months.

Project Start
2000-12-01
Project End
2002-03-31
Budget Start
Budget End
Support Year
41
Fiscal Year
2001
Total Cost
Indirect Cost
Name
Weill Medical College of Cornell University
Department
Type
DUNS #
201373169
City
New York
State
NY
Country
United States
Zip Code
10065
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