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Once Daily Antiretroviral Therapy in HIV Infected Adults Treated With HAART

Primary Purpose

HIV Infections

Status
Completed
Phase
Phase 3
Locations
Study Type
Interventional
Intervention
emtricitabine, FTC (drug)
didanosine, ddI (drug)
efavirenz (drug)
Sponsored by
French National Agency for Research on AIDS and Viral Hepatitis
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for HIV Infections focused on measuring HIV Infections, Reverse Transcriptase Inhibitors, Treatment simplification

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: HIV infected adults Antiretroviral treatment since 6 months, with two nucleoside analogues and one or two protease inhibitors CD4 cell count over 100/mm3 HIV RNA below 400 copies/ml since 6 months Signed written informed consent Exclusion Criteria: Previous treatment with non nucleoside analogue, ddI alone Pregnancy Alcool abuse Acute infection, past neurological or pancreatic disease, biological abnormalities Chemotherapy or immunotherapy

Sites / Locations

    Outcomes

    Primary Outcome Measures

    Virological success from W0 to W48

    Secondary Outcome Measures

    Progression of HIV infection
    CD4 cell count
    Safety
    Treatment adherence
    Quality of life
    Viral mutations
    Therapeutic strategy failure

    Full Information

    First Posted
    September 12, 2005
    Last Updated
    September 12, 2005
    Sponsor
    French National Agency for Research on AIDS and Viral Hepatitis
    Collaborators
    Triangle Pharmaceuticals, Gilead Sciences, Bristol-Myers Squibb, Dupont Applied Biosciences
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    1. Study Identification

    Unique Protocol Identification Number
    NCT00196612
    Brief Title
    Once Daily Antiretroviral Therapy in HIV Infected Adults Treated With HAART
    Official Title
    Phase II Randomized Trial Comparing Efficacy and Safety of the Maintenance of a HAART Association Protease Inhibitor Containing Versus a Once Daily Antiretroviral Triple Association, in HIV Adult Patients With Undetectable Viral Load.ANRS 099 ALIZE
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    September 2005
    Overall Recruitment Status
    Completed
    Study Start Date
    April 2001 (undefined)
    Primary Completion Date
    undefined (undefined)
    Study Completion Date
    September 2004 (undefined)

    3. Sponsor/Collaborators

    Name of the Sponsor
    French National Agency for Research on AIDS and Viral Hepatitis
    Collaborators
    Triangle Pharmaceuticals, Gilead Sciences, Bristol-Myers Squibb, Dupont Applied Biosciences

    4. Oversight

    5. Study Description

    Brief Summary
    The combination of two nucleoside analogues and one protease inhibitor is a highly active antiretroviral therapy (HAART) in HIV infected adults. In those with an undetectable viral load, a once daily combination of FTC, ddI, efavirenz would be easier to take, with less side effects and the same efficacy. The aim of the study was to evaluate if the once daily combination presents the same efficacy than the HAART therapy with less side effects and a better adherence.
    Detailed Description
    The combination of two nucleoside analogues and one protease inhibitor is a highly active antiretroviral therapy (HAART) in HIV infected adults, but side effects an the great number of pills induces less adherence to the therapy. Once daily combination with a lower number of pills could be more easy to take, with a greater adherence, less side effects, and the same efficacy. 355 patients are recruited in the study, randomized in two treatment groups: maintenance of the HAART therapy versus changing for a once daily combination of FTC, ddI, efavirenz, during 48 weeks. The primary end-point is the viral success maintained until 48 weeks. Secondary end-point is the safety and adherence. The trial is prolonged for a total of 48 weeks.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    HIV Infections
    Keywords
    HIV Infections, Reverse Transcriptase Inhibitors, Treatment simplification

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Phase 3
    Interventional Study Model
    Parallel Assignment
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    350 (false)

    8. Arms, Groups, and Interventions

    Intervention Type
    Drug
    Intervention Name(s)
    emtricitabine, FTC (drug)
    Intervention Type
    Drug
    Intervention Name(s)
    didanosine, ddI (drug)
    Intervention Type
    Drug
    Intervention Name(s)
    efavirenz (drug)
    Primary Outcome Measure Information:
    Title
    Virological success from W0 to W48
    Secondary Outcome Measure Information:
    Title
    Progression of HIV infection
    Title
    CD4 cell count
    Title
    Safety
    Title
    Treatment adherence
    Title
    Quality of life
    Title
    Viral mutations
    Title
    Therapeutic strategy failure

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: HIV infected adults Antiretroviral treatment since 6 months, with two nucleoside analogues and one or two protease inhibitors CD4 cell count over 100/mm3 HIV RNA below 400 copies/ml since 6 months Signed written informed consent Exclusion Criteria: Previous treatment with non nucleoside analogue, ddI alone Pregnancy Alcool abuse Acute infection, past neurological or pancreatic disease, biological abnormalities Chemotherapy or immunotherapy
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Jean-Michel Molina, MD, PhD
    Organizational Affiliation
    Service de Maladies Infectieuses, Hôpital Saint-Louis, Paris, 75475, France
    Official's Role
    Principal Investigator
    First Name & Middle Initial & Last Name & Degree
    Genevieve Chene, MD, PhD
    Organizational Affiliation
    INSERM unité 593, Bordeaux, France
    Official's Role
    Study Director

    12. IPD Sharing Statement

    Citations:
    PubMed Identifier
    15717256
    Citation
    Molina JM, Journot V, Morand-Joubert L, Yeni P, Rozenbaum W, Rancinan C, Fournier S, Morlat P, Palmer P, Dupont B, Goujard C, Dellamonica P, Collin F, Poizot-Martin I, Chene G; ALIZE (Agence Nationale de Recherches sur le SIDA 099) Study Team. Simplification therapy with once-daily emtricitabine, didanosine, and efavirenz in HIV-1-infected adults with viral suppression receiving a protease inhibitor-based regimen: a randomized trial. J Infect Dis. 2005 Mar 15;191(6):830-9. doi: 10.1086/428091. Epub 2005 Feb 10.
    Results Reference
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    Once Daily Antiretroviral Therapy in HIV Infected Adults Treated With HAART

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