This study is designed for individuals infected with HIV-1 who are treatment naove, and is designed to examine several strategies for maintaining long-term HIV suppression while minimizing the risk of nonadherence and drug toxicity. The medications used in this study are the FDA-approved medications Combivir (ZDV/3TC), didanosine (ddl, Videx), stavudine (d4T, Zerit), nelfinavir (NFV, Viracept), Indinavir (IDV, Crixivan), hydroxyurea (HU, Droxia), and the investigational drugs efavirenz (EFV, Sustiva) and amprenavir (APV). A four-drug regimen consisting of two NRTIs +NFV + EFV will be compared to two consecutive three-drug regimens consisting of two NRTIs + either NFV or EFV followed by two different NRTIs + NFV for those who initially receive EFV or by two different NRTIs + EFV for those who initially receive NFV (six different randomized inital treatment options). The study will assess which treatment strategy provides the best long-term approach to safe and effective HIV managment, and also compare which strategy is optimal initially.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
General Clinical Research Centers Program (M01)
Project #
3M01RR000046-39S1
Application #
6297299
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 North Carolina Chapel Hill
Department
Type
DUNS #
078861598
City
Chapel Hill
State
NC
Country
United States
Zip Code
27599
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