To evaluate the safety and tolerance of the combination of adefovir dipivoxil at two comparative doses and nelfinavir plus saquinavir SGC administered orally versus the combination of adefovir dipivoxil and nelfinavir plus either AZT, 3TC, or d4T, versus the combination of adefovir dipivoxil and saquinavir SGC plus either AZT, 3TC, or d4T in HIV-1 infected patients with prior nucleoside reverse transcriptase inhibitor therapy but no prior exposure to prokease inhibitors. This study will also determine the proportion of patients whose plasma HIV-I RNA level falls below the level of detection (<500) at 20 weeks and the average reduction in HIV-I RNA from baseline through study week 20.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
General Clinical Research Centers Program (M01)
Project #
3M01RR000040-38A1
Application #
6274559
Study Section
Project Start
1998-04-15
Project End
1998-11-30
Budget Start
1997-10-01
Budget End
1998-09-30
Support Year
38
Fiscal Year
1998
Total Cost
Indirect Cost
Name
University of Pennsylvania
Department
Type
DUNS #
042250712
City
Philadelphia
State
PA
Country
United States
Zip Code
19104
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