drugset / Trial / NCT00144833

Open Label Study of 908/RTV in Combination With Other PIs for the Treatment of Multi PI-Experienced HIV Subjects

NCT00144833

Phase 3 Terminated 150 enrolled GlaxoSmithKline
RandomizedParallel-groupOpen-labelTreatment

Summary

For HIV-infected individuals with highly resistant viruses, higher drug levels may be required to block the virus. This study investigates that concept by comparing the efficacy of standard fosamprenavir/ritonavir to an increased dose of boosted fosamprenavir and to a combination of fosamprenavir (increased dose)/lopinavir/ritonavir.

Timeline

Start
2005-03
Primary completion
Completion

Drugs

EvaluationDrugModalityDoseRoute
Subject Fosamprenavir Small molecule 700 mg
Subject Fosamprenavir Small molecule 1400 mg
Subject Lopinavir Other / unclassified 533 mg
Background Ritonavir Other / unclassified 100 mg

Indications

No indication recorded.