HIV Infections
Conditions
Keywords
HIV-1, Drug Therapy, Combination, Acquired Immunodeficiency Syndrome, HIV Protease Inhibitors, RNA, Viral, Saquinavir, Anti-HIV Agents, Viral Load
Brief summary
To examine the efficacy of saquinavir SGC (soft gel capsules) in combination with other antiretrovirals in HIV-1 infected patients currently treated with saquinavir HGC (hard gel capsules) measured by the absolute change in plasma HIV-1 RNA during the 24 weeks of study treatment.
Detailed description
Eligible patients will be stratified by HIV-1 RNA level into 2 populations: 1) \>= 5,000-30,000 HIV-1 RNA, 2) \> 30,000 HIV-1 RNA. All patients will be randomized to 1 of 3 treatment arms: Arm A - Saquinavir soft gel capsules (SQV SGC) + 2 new nucleoside analogs (reverse transcriptase inhibitors \[RTIs\]), Arm B - SQV SGC + nelfinavir + stavudine (d4T) or a new RTI, or Arm C - SQV SGC + ritonavir + d4T or a new RTI. All patients will undergo plasma HIV-1 RNA determinations, CD4 lymphocyte counts, hematology and chemistry blood work at baseline, weeks 4, 8, 12, 16 and 24.
Interventions
Sponsors
Study design
Eligibility
Inclusion criteria
Patients must have: * Documented HIV infection. * CD4 \> 100 cells/mm3. * Saquinavir HGC-experienced patients (\>= 3 months cumulative therapy). Required: \>= 3 months cumulative saquinavir HGC therapy.
Countries
United States