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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.

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Trial Profile

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.

Status: Completed
Phase of Trial: Phase III

Latest Information Update: 04 Jul 2023

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At a glance

  • Drugs Lamivudine/abacavir (Primary) ; Abacavir; Lamivudine
  • Indications HIV-1 infections
  • Focus Registrational; Therapeutic Use
  • Sponsors GlaxoSmithKline; GSK

    • Most Recent Events

    • 20 May 2009 Actual initiation date changed from Aug 2002 to Jul 2002 as reported by ClinicalTrials.gov.
    • 24 Mar 2009 Primary endpoints identified as clinical response as reported by ClinicalTrials.gov.
    • 24 Mar 2009 Planned number of patients changed to 166 as reported by ClinicalTrials.gov.

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