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HIV Immune and Virological Responses Following the Administration of IL-2 Either Alone or Combined to ALVAC-HIV 1433 and HIV Lipopeptides in Patients Treated Early With HAART During Primary Infection

Primary Purpose

HIV Infection

Status
Terminated
Phase
Phase 2
Locations
Study Type
Interventional
Intervention
IL-2
LIPO-6T
ALVAC VIH 1433
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 Infection focused on measuring HIV infection, AIDS Vaccines, ALVAC vaccine, Interleukin-2, Antiretroviral Therapy, Highly Active

Eligibility Criteria

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

Inclusion Criteria: History of symptomatic HIV primary infection with p24 positive or incomplete Western Blot Treatment beginning before 4W after the first primary infection serology HAART with IP or NNRTI since one year, wtih no change since 3 months Viral load below 50 cp since 6 months PN over 1000/mm3;Hb over 10.5g/l;Platelets over 75000/mm3, creatinine below 1.5N; transaminases below 2.5N Exclusion Criteria: Vaccination or chemotherapy or corticosteroid since 3 months Evolutive cancer pregnancy or breastfeeding

Sites / Locations

    Outcomes

    Primary Outcome Measures

    Evolution of CD4-CD8 non specific and HIV specific cells, vaccinal peptids and viral load with DNA proviral at W36

    Secondary Outcome Measures

    Safety of IL-2, ALVAC and LIPO-6T
    Tolerability of HAART
    Kinetic of viral load rebound with frequency and delay of cv over 10 000 cp and 50 000 cp
    Evolution on immune response and predictive value of immunologic parameters on viral load

    Full Information

    First Posted
    September 12, 2005
    Last Updated
    September 12, 2005
    Sponsor
    French National Agency for Research on AIDS and Viral Hepatitis
    Collaborators
    Aventis Pharmaceuticals
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    1. Study Identification

    Unique Protocol Identification Number
    NCT00196651
    Brief Title
    HIV Immune and Virological Responses Following the Administration of IL-2 Either Alone or Combined to ALVAC-HIV 1433 and HIV Lipopeptides in Patients Treated Early With HAART During Primary Infection
    Official Title
    Randomized Study on HIV Immune and Virological Responses Following the Administration of IL-2 Either Alone or Combined to ALVAC-HIV 1433 and HIV Lipopeptides (LIPO-6T) in Patients Treated Early With HAART During Primary Infection. ANRS 095 PRIMOVAC
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    September 2005
    Overall Recruitment Status
    Terminated
    Study Start Date
    August 2000 (undefined)
    Primary Completion Date
    undefined (undefined)
    Study Completion Date
    February 2004 (undefined)

    3. Sponsor/Collaborators

    Name of the Sponsor
    French National Agency for Research on AIDS and Viral Hepatitis
    Collaborators
    Aventis Pharmaceuticals

    4. Oversight

    5. Study Description

    Brief Summary
    HIV-specific immune responses are preserved in patients treated early during primary infection.The trial evaluated whether the addition to HAART of IL-2 alone or combined with an immunization procedure might enhance HIV immune responses and improve viral control after HAART discontinuation
    Detailed Description
    HIV-specific immune responses are preserved in patients treated early during primary infection. The trial evaluated whether the addition to HAART of IL-2 alone or combined with an immunization procedure might enhance HIV immune responses and improve viral control after HAART discontinuation.Patients treated with HAART are randomized to 3 arms:arm1 HAART alone; arm2 with 5 cycles of IL-2 at wk0 ,8 ,16 ,24 and 32;arm3 4 injections of Alvac-HIV 1433 and LIPO-6T at wk0,4,8 followed by 3 cycles of IL-2 at w 16, 24 and 32. HAART is stopped at wk 40 in patient with undetectable plasma viral load. Viral loads and HIV-specific responses are monitored during the therapeutic period and after HAART interruption until w52. HAARTis rei-initiated with viral failure.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    HIV Infection
    Keywords
    HIV infection, AIDS Vaccines, ALVAC vaccine, Interleukin-2, Antiretroviral Therapy, Highly Active

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Phase 2
    Interventional Study Model
    Parallel Assignment
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    60 (false)

    8. Arms, Groups, and Interventions

    Intervention Type
    Drug
    Intervention Name(s)
    IL-2
    Intervention Type
    Biological
    Intervention Name(s)
    LIPO-6T
    Intervention Type
    Biological
    Intervention Name(s)
    ALVAC VIH 1433
    Primary Outcome Measure Information:
    Title
    Evolution of CD4-CD8 non specific and HIV specific cells, vaccinal peptids and viral load with DNA proviral at W36
    Secondary Outcome Measure Information:
    Title
    Safety of IL-2, ALVAC and LIPO-6T
    Title
    Tolerability of HAART
    Title
    Kinetic of viral load rebound with frequency and delay of cv over 10 000 cp and 50 000 cp
    Title
    Evolution on immune response and predictive value of immunologic parameters on viral load

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: History of symptomatic HIV primary infection with p24 positive or incomplete Western Blot Treatment beginning before 4W after the first primary infection serology HAART with IP or NNRTI since one year, wtih no change since 3 months Viral load below 50 cp since 6 months PN over 1000/mm3;Hb over 10.5g/l;Platelets over 75000/mm3, creatinine below 1.5N; transaminases below 2.5N Exclusion Criteria: Vaccination or chemotherapy or corticosteroid since 3 months Evolutive cancer pregnancy or breastfeeding
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Cecile Goujard, MD
    Organizational Affiliation
    Hopital Kremlin Bicetre Bicetre France
    Official's Role
    Principal Investigator
    First Name & Middle Initial & Last Name & Degree
    Jean Pierre Aboulker, MD
    Organizational Affiliation
    Inserm SC10 France
    Official's Role
    Study Director

    12. IPD Sharing Statement

    Citations:
    PubMed Identifier
    17919105
    Citation
    Goujard C, Marcellin F, Hendel-Chavez H, Burgard M, Meiffredy V, Venet A, Rouzioux C, Taoufik Y, El Habib R, Beumont-Mauviel M, Aboulker JP, Levy Y, Delfraissy JF; PRIMOVAC-ANRS 095 Study Group. Interruption of antiretroviral therapy initiated during primary HIV-1 infection: impact of a therapeutic vaccination strategy combined with interleukin (IL)-2 compared with IL-2 alone in the ANRS 095 Randomized Study. AIDS Res Hum Retroviruses. 2007 Sep;23(9):1105-13. doi: 10.1089/aid.2007.0047.
    Results Reference
    derived

    Learn more about this trial

    HIV Immune and Virological Responses Following the Administration of IL-2 Either Alone or Combined to ALVAC-HIV 1433 and HIV Lipopeptides in Patients Treated Early With HAART During Primary Infection

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