drugset / Trial / NCT00335270

A Randomized, Prospective Study of the Efficacy, Safety and Tolerability of Two Doses of GW433908Ritonavir Given With Abacavir/Lamivudine Fixed Dose Combination

NCT00335270

Phase 4 Completed 100 enrolled Duke University GlaxoSmithKline · collab
RandomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate the antiretroviral efficacy, safety, and tolerability of fos-amprenavir boosted with either of two doses of ritonavir (RTV) when administered in combination with ABC/3TC (abacavir/lamivudine, Epzicom®) FDC (fixed dose combination) in a once-daily regimen over 96 weeks in ART-naïve, HIV-infected adults

Timeline

Start
2006-03
Primary completion
2007-12
Completion
2007-12

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Fosamprenavir Small molecule 1400 mg
Subject Ritonavir Other / unclassified 100 mg
Subject Ritonavir Other / unclassified 200 mg
Background Abacavir Other / unclassified 600 mg
Background Lamivudine Other / unclassified 300 mg