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Antibody Responses to Pneumococcal Vaccines Among HIV-Infected Adults.

Primary Purpose

HIV Infections

Status
Completed
Phase
Phase 2
Locations
Study Type
Interventional
Intervention
7-valent pneumococcal conjugate vaccine (vaccine)
23-valent pneumococcal conjugate vaccine (vaccine)
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 prevention trial for HIV Infections focused on measuring HIV infections, Pneumococcal vaccines, Treatment Experienced, Treatment Naive

Eligibility Criteria

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

Inclusion Criteria: Adult patients with proven HIV-1 infection Naïve or antiretroviral experienced CD4 cell count between 200 and 500/mm3 Plasma HIV RNA load lower than 4 log10 copies/mL Signed written informed consent Exclusion Criteria: Immunotherapy Immunization with the PPV within the past 5 years Splenectomy Use of intravenous immunoglobulin within the past 2 months Chemotherapy or radiation Any other vaccination within the past 2 months Severe renal failure End-stage liver disease Pregnancy

Sites / Locations

    Outcomes

    Primary Outcome Measures

    Proportion of patients responders to 7 pneumococcal polysaccharides at W8

    Secondary Outcome Measures

    Persistence of antibody responses at W24 and W96
    Clinical tolerance of pneumococcal vaccines at W8
    Evolution of the CD4 count and plasma HIV RNA load
    Immunological substudy (predictive factors of the antibody responses) at W24

    Full Information

    First Posted
    September 7, 2005
    Last Updated
    March 20, 2008
    Sponsor
    French National Agency for Research on AIDS and Viral Hepatitis
    Collaborators
    Wyeth is now a wholly owned subsidiary of Pfizer
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    1. Study Identification

    Unique Protocol Identification Number
    NCT00148824
    Brief Title
    Antibody Responses to Pneumococcal Vaccines Among HIV-Infected Adults.
    Official Title
    Immunological Efficacy of a Prime-Boost Strategy Combining a 7-Valent Pneumococcal Conjugate Vaccine (PCV) Followed by a 23-Valent Pneumococcal Polysaccharide Vaccine (PPV) Versus PPV Alone in HIV-Infected Adults. ANRS 114 PNEUMOVAC.
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    March 2008
    Overall Recruitment Status
    Completed
    Study Start Date
    February 2003 (undefined)
    Primary Completion Date
    undefined (undefined)
    Study Completion Date
    January 2006 (Actual)

    3. Sponsor/Collaborators

    Name of the Sponsor
    French National Agency for Research on AIDS and Viral Hepatitis
    Collaborators
    Wyeth is now a wholly owned subsidiary of Pfizer

    4. Oversight

    5. Study Description

    Brief Summary
    Streptococcus pneumoniae is the major cause of bacterial infection in HIV-infected patients. The current pneumococcal vaccine is poorly efficacious in patients with a CD4 cell count lower than 500/mm3. This study will test the efficacy and safety of a new pneumococcal vaccine strategy in patients with a CD4 cell count between 200 and 500/mm3.
    Detailed Description
    Streptococcus pneumoniae (SP) is the major cause of bacterial infection in HIV-infected patients. The 23-valent pneumococcal polysaccharide (PPV) is poorly immunogenic in patients with CD4 below 500 cells/mm3. The purpose of this multicentric national study is to evaluate whether a prime with a 7-valent pneumococcal conjugate vaccine (PCV), able to induce immunological memory, would improve immunogenicity against SP polysaccharides. 212 HIV-1 infected patients, with a CD4 count between 200 and 500/mm3, will be randomly assigned to one of two vaccine groups: PCV at Week 0 followed by PPV at Week 4 or PPV alone at Week 4. Evaluation will be done at week 8. The primary endpoint is the proportion of patients who had antibody responses against 7 pneumococcal polysaccharides at Week 8. Secondary endpoints include the persistence of antibody responses at Weeks 24 and 96, vaccines safety and occurrence of pneumococcal disease over time.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    HIV Infections
    Keywords
    HIV infections, Pneumococcal vaccines, Treatment Experienced, Treatment Naive

    7. Study Design

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

    8. Arms, Groups, and Interventions

    Intervention Type
    Biological
    Intervention Name(s)
    7-valent pneumococcal conjugate vaccine (vaccine)
    Intervention Type
    Biological
    Intervention Name(s)
    23-valent pneumococcal conjugate vaccine (vaccine)
    Primary Outcome Measure Information:
    Title
    Proportion of patients responders to 7 pneumococcal polysaccharides at W8
    Secondary Outcome Measure Information:
    Title
    Persistence of antibody responses at W24 and W96
    Title
    Clinical tolerance of pneumococcal vaccines at W8
    Title
    Evolution of the CD4 count and plasma HIV RNA load
    Title
    Immunological substudy (predictive factors of the antibody responses) at W24

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Adult patients with proven HIV-1 infection Naïve or antiretroviral experienced CD4 cell count between 200 and 500/mm3 Plasma HIV RNA load lower than 4 log10 copies/mL Signed written informed consent Exclusion Criteria: Immunotherapy Immunization with the PPV within the past 5 years Splenectomy Use of intravenous immunoglobulin within the past 2 months Chemotherapy or radiation Any other vaccination within the past 2 months Severe renal failure End-stage liver disease Pregnancy
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Philippe Lesprit, MD
    Organizational Affiliation
    Service d'Immunologie Clinique, Créteil, 94010, France
    Official's Role
    Principal Investigator
    First Name & Middle Initial & Last Name & Degree
    Geneviève Chêne, MD, PhD
    Organizational Affiliation
    INSERM unité 593
    Official's Role
    Study Director

    12. IPD Sharing Statement

    Citations:
    PubMed Identifier
    20210645
    Citation
    Rabian C, Tschope I, Lesprit P, Katlama C, Molina JM, Meynard JL, Delfraissy JF, Chene G, Levy Y; ANRS 114 Pneumovac Study Group. Cellular CD4 T cell responses to the diphtheria-derived carrier protein of conjugated pneumococcal vaccine and antibody response to pneumococcal vaccination in HIV-infected adults. Clin Infect Dis. 2010 Apr 15;50(8):1174-83. doi: 10.1086/651418.
    Results Reference
    derived

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    Antibody Responses to Pneumococcal Vaccines Among HIV-Infected Adults.

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