The purpose of this NIAID-sponsored, multicenter, randomized study is to compare the safety, tolerance and effectiveness of two different routes of administration of recombinant human interleukin-2 (rhIL-2) in combination with highly active antiretroviral therapy (HAART), to HAART alone as treatment for human immunodeficiency type one (HIV) infection. rhIL-2 will be administered, either as 7.5 MIU BID subcutaneously for 5 days every 8 weeks or as 9 MIU by continuous intravenouws infusion for 5 days every 8 weeks, for a total of 72 weeks. In this protocol, HAART consists of one of four triple combinations of indinavir (IDV) a potent protease inhibitor plus 2 nucleosides. Subjects randomized to receive continuous infusion rhIL-2 will be hospitalized at the UWMC GCRC for the first 5-day cycle of rhIL-2.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
General Clinical Research Centers Program (M01)
Project #
3M01RR000037-39S1
Application #
6263530
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 Washington
Department
Type
DUNS #
135646524
City
Seattle
State
WA
Country
United States
Zip Code
98195
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