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Safety and efficacy of an initial regimen of atazanavir + ritonavir + the abacavir/lamivudine fixed-dose combination tablet (ABC/3TC FDC) for 36 weeks followed by simplification to atazanavir with ABC/3TC FDC or maintenance of the initial regimen for an additional 48 weeks in antiretroviral-naive HIV-1 infected HLA-B5701 negative subjects

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Trial Profile

Safety and efficacy of an initial regimen of atazanavir + ritonavir + the abacavir/lamivudine fixed-dose combination tablet (ABC/3TC FDC) for 36 weeks followed by simplification to atazanavir with ABC/3TC FDC or maintenance of the initial regimen for an additional 48 weeks in antiretroviral-naive HIV-1 infected HLA-B5701 negative subjects

Status: Completed
Phase of Trial: Phase III

Latest Information Update: 05 Sep 2023

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At a glance

  • Drugs Atazanavir (Primary) ; Lamivudine/abacavir (Primary) ; Ritonavir (Primary)
  • Indications HIV-1 infections
  • Focus Registrational; Therapeutic Use
  • Acronyms ARIES
  • Sponsors ViiV Healthcare

    • Most Recent Events

    • 20 Jul 2011 Long-term extension study results presented at the 6th International AIDS Society Conference on HIV Pathogenesis and Treatment.
    • 24 Nov 2010 Actual end date (Jul 2010) added as reported by ClinicalTrials.gov.
    • 24 Nov 2010 Status changed from active, no longer recruiting to completed as reported by ClinicalTrials.gov.

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