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New Tablet Containing Two FDA Approved Anti-HIV Drugs For Antiretroviral Therapy Experienced HIV-1 Infected Subjects

HIV Infection Clinical Trial

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Clinical Trial Summary

A 48-week study to investigate the safety and effectiveness of a new compact formulation of two already FDA-approved anti-HIV drugs in subjects who have already been receiving treatment for their HIV infection.

Clinical Trial Description

A phase III, randomized, open-label, parallel, multicenter study to evaluate treatment with fixed-dose combination of abacavir/lamivudine (600mg/300mg) once-daily versus abacavir (300mg) twice-daily and lamivudine (300mg) once-daily in combination with tenofovir once-daily and a new PI or NNRTI for 48 weeks in ART-experienced HIV-1 infected patients. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00044577
Study type Interventional
Source ViiV Healthcare
Contact
Status Completed
Phase Phase 3
Start date July 16, 2002
Completion date May 25, 2004
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