drugset / Trial / NCT00122603
Dual Boosted Protease Inhibitor Regimens Without Any Additional Antiretroviral Therapy in HIV-1 Infected Patients (ANRS127)
Phase 2
Completed
61 enrolled
French National Agency for Research on AIDS and Viral Hepatitis
Bristol-Myers Squibb · collabGlaxoSmithKline · collabHoffmann-La Roche · collab
RandomizedParallel-groupOpen-labelTreatment
Summary
The purpose of this study is to evaluate virological efficacy and safety of two double protease inhibitor regimens: atazanavir/fosamprenavir/ritonavir 300 mg once daily/ 700/100 mg twice daily, versus atazanavir/saquinavir/ritonavir 300/1500/100 mg once daily in protease inhibitor naive HIV-1 patients.
Timeline
- Start
- 2005-12
- Primary completion
- —
- Completion
- 2007-08
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Fosamprenavir | Small molecule | 700 mg | — |
| Subject | Saquinavir | Small molecule | 500 mg | — |
| Background | Atazanavir | Other / unclassified | 150 mg | — |
| Background | Ritonavir | Other / unclassified | 100 mg | — |