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Non-inferiority,randomized clinical trial to evaluate the efficacy and the safety of the use of fixed-dose combination efavirenz/tenofovir/emtricitabine (Atripla) administered in alternate days versus the standard of care in HIV-1 infected patients with sustained virological response during HAART [Studio clinico randomizzato di non inferiorita sulla efficacia e sicurezza dell uso di efavirenz/tenofovir/emtricitabina in combinazione fissa (Atripla) somministrato a giorni alterni comparato con lo standard of care in pazienti con infezione da HIV-1 in soppressione virologica sotto HAART].

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Trial Profile

Non-inferiority,randomized clinical trial to evaluate the efficacy and the safety of the use of fixed-dose combination efavirenz/tenofovir/emtricitabine (Atripla) administered in alternate days versus the standard of care in HIV-1 infected patients with sustained virological response during HAART [Studio clinico randomizzato di non inferiorita sulla efficacia e sicurezza dell uso di efavirenz/tenofovir/emtricitabina in combinazione fissa (Atripla) somministrato a giorni alterni comparato con lo standard of care in pazienti con infezione da HIV-1 in soppressione virologica sotto HAART].

Status: Completed
Phase of Trial: Phase III

Latest Information Update: 17 Feb 2019

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At a glance

  • Drugs Efavirenz/emtricitabine/tenofovir-disoproxil-fumarate (Primary)
  • Indications HIV-1 infections
  • Focus Pharmacogenomic; Therapeutic Use

    • Most Recent Events

    • 05 Feb 2019 Status changed from recruiting to completed.
    • 05 Feb 2019 Results published in the AIDS
    • 06 Sep 2012 New trial record

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