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Vaccination Against Influenza H1N1 in Rheumatic Diseases

Primary Purpose

Influenza, Rheumatic Diseases

Status
Unknown status
Phase
Phase 2
Locations
Study Type
Interventional
Intervention
Focetria (Monovalent MF59-Adjuvanted vaccine)
Focetria (Monovalent MF59-Adjuvanted vaccine)
Focetria (Monovalent MF59-Adjuvanted vaccine)
Sponsored by
Tel-Aviv Sourasky Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Influenza focused on measuring rheumatoid, SLE, Psoriatic arthritis, Ankylosing, Influenza H1N1, Vaccine, Vaccination against H1N1 in rheumatic diseases

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Patients suffering from: Rheumatoid Arthritis, Systemic Lupus Erythematosus, Ankylosing Spondylitis, Psoriatic Arthritis
  • Able to firm an informed consent
  • Aged - 18-65
  • Candidates to receive vaccination against H1N1, according to the recommendation of the Ministry of Health

Exclusion Criteria:

  • Allergy to eggs
  • Known allergy to seasonal influenza vaccine
  • Pregnant women

Sites / Locations

    Arms of the Study

    Arm 1

    Arm Type

    Experimental

    Arm Label

    Monovalent MF59-Adjuvanted vaccine

    Arm Description

    Outcomes

    Primary Outcome Measures

    Primary Endpoint : Proportion of patients who will achieve a titer of antibodies above 1/40 within the groups of patients in comparison with healthy subjects

    Secondary Outcome Measures

    Secondary Endpoint: Safety of the vaccine with regard to disease activity by changes in DAS, SLEDAI and BASDAI

    Full Information

    First Posted
    October 31, 2009
    Last Updated
    November 2, 2009
    Sponsor
    Tel-Aviv Sourasky Medical Center
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    1. Study Identification

    Unique Protocol Identification Number
    NCT01006681
    Brief Title
    Vaccination Against Influenza H1N1 in Rheumatic Diseases
    Official Title
    Efficacy and Safety of Vaccination Against Influenza H1N1 in Patients With Rheumatoid Arthritis, Systemic Lupus Erythematosus, Psoriatic Arthritis and Ankylosing Spondylitis Treated With Immunomodulatory Drugs
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    November 2009
    Overall Recruitment Status
    Unknown status
    Study Start Date
    November 2009 (undefined)
    Primary Completion Date
    April 2010 (Anticipated)
    Study Completion Date
    April 2010 (Anticipated)

    3. Sponsor/Collaborators

    Name of the Sponsor
    Tel-Aviv Sourasky Medical Center

    4. Oversight

    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    The spread of Influenza H1N1 has prompted the development of vaccines against this virus. Immunocompromised patients are at increased risk of developing complications of Influenza H1N1. The efficacy and safety of H1N1 vaccination have not been evaluated in this population of patients.
    Detailed Description
    100 patients with Rheumatoid Arthritis (RA), 50 patients with Systemic Lupus Erythematosus (SLE), 50 patients with spondyloarthropathies (Psoriatic arthritis (PsA) and Ankylosing Spondylitis (AS) and 200 healthy subjects will participate in the study. All the subjects will be vaccinated with Focetria (Novartis) and will be evaluated the day of vaccination and 4 weeks later. The evaluation will include: Efficacy of the vaccine: Blood will be drawn on day 0 and 4 weeks later and tested for the presence of antibodies against A/California17/2009/H1N1 by hemagglutination inhibition test. Safety of the vaccine: Records of adverse event Assessment of disease activity : RA - Disease activity score (DAS 28), SLE - SLEDAI, PsA - DAS 28 and PASI, AS- BASDAI, ESR, CRP

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Influenza, Rheumatic Diseases
    Keywords
    rheumatoid, SLE, Psoriatic arthritis, Ankylosing, Influenza H1N1, Vaccine, Vaccination against H1N1 in rheumatic diseases

    7. Study Design

    Primary Purpose
    Prevention
    Study Phase
    Phase 2
    Interventional Study Model
    Single Group Assignment
    Masking
    None (Open Label)
    Allocation
    Non-Randomized
    Enrollment
    400 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Monovalent MF59-Adjuvanted vaccine
    Arm Type
    Experimental
    Intervention Type
    Biological
    Intervention Name(s)
    Focetria (Monovalent MF59-Adjuvanted vaccine)
    Other Intervention Name(s)
    Focetria
    Intervention Description
    7.5 mcg Hemagglutinin H1/InfluezaA/California/7/2009 ,9.75 mg squalene MF59, 1.175 mg polysort80, 1.175 mg sorbitan trioleate Intra muscular
    Intervention Type
    Biological
    Intervention Name(s)
    Focetria (Monovalent MF59-Adjuvanted vaccine)
    Other Intervention Name(s)
    Focetria
    Intervention Description
    7.5 mg Hemagglutinin H1/InfluezaA/California/7/2009, 9.75 mg squalene MF59, 1.175 mg polysirate 80, 1.175 mg sorbitan trioleate Intramuscular injection
    Intervention Type
    Biological
    Intervention Name(s)
    Focetria (Monovalent MF59-Adjuvanted vaccine)
    Other Intervention Name(s)
    Focetria
    Intervention Description
    Monovalent MF59-Adjuvanted vaccine
    Primary Outcome Measure Information:
    Title
    Primary Endpoint : Proportion of patients who will achieve a titer of antibodies above 1/40 within the groups of patients in comparison with healthy subjects
    Time Frame
    4 weeks
    Secondary Outcome Measure Information:
    Title
    Secondary Endpoint: Safety of the vaccine with regard to disease activity by changes in DAS, SLEDAI and BASDAI
    Time Frame
    4 weeks

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Maximum Age & Unit of Time
    65 Years
    Accepts Healthy Volunteers
    Accepts Healthy Volunteers
    Eligibility Criteria
    Inclusion Criteria: Patients suffering from: Rheumatoid Arthritis, Systemic Lupus Erythematosus, Ankylosing Spondylitis, Psoriatic Arthritis Able to firm an informed consent Aged - 18-65 Candidates to receive vaccination against H1N1, according to the recommendation of the Ministry of Health Exclusion Criteria: Allergy to eggs Known allergy to seasonal influenza vaccine Pregnant women

    12. IPD Sharing Statement

    Citations:
    PubMed Identifier
    21425247
    Citation
    Elkayam O, Amir S, Mendelson E, Schwaber M, Grotto I, Wollman J, Arad U, Brill A, Paran D, Levartovsky D, Wigler I, Caspi D, Mandelboim M. Efficacy and safety of vaccination against pandemic 2009 influenza A (H1N1) virus among patients with rheumatic diseases. Arthritis Care Res (Hoboken). 2011 Jul;63(7):1062-7. doi: 10.1002/acr.20465.
    Results Reference
    derived

    Learn more about this trial

    Vaccination Against Influenza H1N1 in Rheumatic Diseases

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