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MF59-adjuvanted Influenza Vaccine and 23-valent Pneumococcal Polysaccharide Vaccine

Primary Purpose

Influenza, Human, Pneumococcal Infections

Status
Completed
Phase
Phase 4
Locations
Study Type
Interventional
Intervention
Fluad alone
Fluad and PPV23 on the different arms
Fluad and PPV23 on the same arm
PPV23 alone
Sponsored by
Korea University Guro Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Influenza, Human

Eligibility Criteria

65 Years - undefined (Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • At least 65 years of age who are eligible for the study vaccines;
  • Who have given written informed consent at the time of enrollment);
  • Those who are available for all the visits scheduled in the study;
  • Subjects In good health as determined by medical history, physical examination and clinical judgment of the investigator

Exclusion Criteria:

  • History of egg allergy
  • History of influenza vaccination in previous 6 months
  • History of any pneumococcal vaccination
  • Documented S. pneumonia infection in the previous 5 years
  • Chemotherapy for malignancy within the past 30 days
  • High-dose systemic steroid (prednisone ≥0.5 mg/kg/day) in the past 30 days
  • Receipt of blood product within 6 months before enrollment
  • Significant acute or chronic infection within the previous 7 days or fever within the previous day
  • Any serious chronic or progressive disease
  • Any condition that might interfere with the study results.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm 3

    Arm 4

    Arm Type

    Active Comparator

    Active Comparator

    Active Comparator

    Active Comparator

    Arm Label

    Fluad alone

    Fluad and PPV23 on the different arms

    Fluad and PPV23 on the same arm

    PPV23 alone

    Arm Description

    56 Fluad recipients: one vaccine injection administered on Day 0

    56 concomitant Fluad-PPV23 recipients on the different arms: one dose of each vaccine administered on Day 0

    56 concomitant Fluad-PPV23 recipients on the same arm with 1 inch distance: one dose of each vaccine administered on Day 0

    56 PPV23 recipients: one vaccine injection administered on Day 0

    Outcomes

    Primary Outcome Measures

    Seroconversion rates (A/H1N1, A/H3N2, and B)
    a post-vaccination titer ≥1:40 in subjects with a pre-vaccination titer of <1:10 or a ≥4-fold titer increase in subjects with a pre-vaccination titer of ≥1:10

    Secondary Outcome Measures

    Seroprotection rates (A/H1N1, A/H3N2, and B)
    Percentage of subjects with a post-vaccination titer ≥1:40
    GMT folds (A/H1N1, A/H3N2, and B)
    GMT-fold change: GMT ratio of the post-vaccination titer to pre-vaccination titer
    Opsonophagocytic assay (OPA) titers for four serotypes of PPV23 (serotypes 5, 6B, 18C and 19A)
    OPA geometric mean titers for four PPV23 serotypes with corresponding 2-sided 95% confidence intervals will be compared between groups receiving PPV23: MF59-adjuvanted TIV + PPV23 at different arm, MF59-adjuvanted TIV + PPV23 at same arm and PPV23 alone.

    Full Information

    First Posted
    August 22, 2014
    Last Updated
    August 26, 2014
    Sponsor
    Korea University Guro Hospital
    Collaborators
    Novartis
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    1. Study Identification

    Unique Protocol Identification Number
    NCT02225327
    Brief Title
    MF59-adjuvanted Influenza Vaccine and 23-valent Pneumococcal Polysaccharide Vaccine
    Official Title
    Immunogenicity and Safety of MF59-adjuvanted Trivalent Influenza Vaccine (Fluad) and 23-valent Pneumococcal Polysaccharide Vaccine (PPV23) in the Elderly: Single Versus Concomitant Vaccination
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    August 2014
    Overall Recruitment Status
    Completed
    Study Start Date
    October 2013 (undefined)
    Primary Completion Date
    December 2013 (Actual)
    Study Completion Date
    January 2014 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Korea University Guro Hospital
    Collaborators
    Novartis

    4. Oversight

    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    Similar to children, adults frequently visit outpatient clinics to get two or more kinds of vaccines at the same time: pneumococcal vaccine, influenza vaccine, Td (diphtheria and tetanus) vaccine, HPV (human papilloma virus) vaccine, meningococcal vaccine, zoster vaccine, etc. This study is intended to evaluate the immunogenicity and safety of concomitant administration of 23-valent pneumococcal polysaccharide vaccine (PPV23, Prodiax) and MF59 adjuvanted trivalent influenza vaccine in the elderly subjects aged ≥65 years.
    Detailed Description
    During influenza season, concomitant influenza and pneumococcal vaccination would be an effective strategy to enhance pneumococcal vaccine coverage rate in high-risk adults. However, the immunogenicity and safety of concomitant vaccination need to be further investigated. There is data on immunogenicity and safety after concomitant administration of pneumococcal polysaccharide vaccine (PPV) and unadjuvanted influenza vaccine; no interference was noted between two vaccines. However, there are no data for MF59 adjuvanted influenza vaccine with pneumococcal vaccine. MF59 only locally reacts for immune response, so immunogenicity should be assessed for both vaccines injected in same arm versus different arms. This study is intended to evaluate the immunogenicity and safety of concomitant MF59-adjuvanted trivalent influenza vaccine (MF59-aTIV, Fluad) and 23-valent pneumococcal polysaccharide vaccine (PPV23, Prodiax) vaccination in the elderly subjects aged ≥65 years. Healthy elderly subjects (N = 424) are randomized in a 1:1:1:1 ratio to receive MF59-aTIV alone (group 1), MF59-aTIV +PPV23 at different arm (group 2), MF59-aTIV +PPV23 at same arm (group 3) or PPV23 alone (group 4). Hemagglutination inhibition (HI) assay and multiplex opsono-phagocytic killing assay (MOPA) will be used to compare the immunogenicity of each vaccine after single or concomitant vaccination at pre-vaccination and 1 month post-vaccination. MOPA will be taken for four serotypes (5, 6B, 18C and 19A).

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Influenza, Human, Pneumococcal Infections

    7. Study Design

    Primary Purpose
    Prevention
    Study Phase
    Phase 4
    Interventional Study Model
    Parallel Assignment
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    224 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    Fluad alone
    Arm Type
    Active Comparator
    Arm Description
    56 Fluad recipients: one vaccine injection administered on Day 0
    Arm Title
    Fluad and PPV23 on the different arms
    Arm Type
    Active Comparator
    Arm Description
    56 concomitant Fluad-PPV23 recipients on the different arms: one dose of each vaccine administered on Day 0
    Arm Title
    Fluad and PPV23 on the same arm
    Arm Type
    Active Comparator
    Arm Description
    56 concomitant Fluad-PPV23 recipients on the same arm with 1 inch distance: one dose of each vaccine administered on Day 0
    Arm Title
    PPV23 alone
    Arm Type
    Active Comparator
    Arm Description
    56 PPV23 recipients: one vaccine injection administered on Day 0
    Intervention Type
    Biological
    Intervention Name(s)
    Fluad alone
    Intervention Description
    Fluad
    Intervention Type
    Biological
    Intervention Name(s)
    Fluad and PPV23 on the different arms
    Intervention Description
    Fluad and Prodiax
    Intervention Type
    Biological
    Intervention Name(s)
    Fluad and PPV23 on the same arm
    Intervention Description
    Fluad and Prodiax
    Intervention Type
    Biological
    Intervention Name(s)
    PPV23 alone
    Intervention Description
    Prodiax
    Primary Outcome Measure Information:
    Title
    Seroconversion rates (A/H1N1, A/H3N2, and B)
    Description
    a post-vaccination titer ≥1:40 in subjects with a pre-vaccination titer of <1:10 or a ≥4-fold titer increase in subjects with a pre-vaccination titer of ≥1:10
    Time Frame
    Outcome measure will be assessed at two points (baseline and 4 weeks after vaccination)
    Secondary Outcome Measure Information:
    Title
    Seroprotection rates (A/H1N1, A/H3N2, and B)
    Description
    Percentage of subjects with a post-vaccination titer ≥1:40
    Time Frame
    Outcome measure will be assessed at two points (baseline and 4 weeks after vaccination).
    Title
    GMT folds (A/H1N1, A/H3N2, and B)
    Description
    GMT-fold change: GMT ratio of the post-vaccination titer to pre-vaccination titer
    Time Frame
    Outcome measure will be assessed at two points (baseline and 4 weeks after vaccination.
    Title
    Opsonophagocytic assay (OPA) titers for four serotypes of PPV23 (serotypes 5, 6B, 18C and 19A)
    Description
    OPA geometric mean titers for four PPV23 serotypes with corresponding 2-sided 95% confidence intervals will be compared between groups receiving PPV23: MF59-adjuvanted TIV + PPV23 at different arm, MF59-adjuvanted TIV + PPV23 at same arm and PPV23 alone.
    Time Frame
    Outcome measure will be assessed at two points (baseline and 4 weeks after vaccination).

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    65 Years
    Accepts Healthy Volunteers
    Accepts Healthy Volunteers
    Eligibility Criteria
    Inclusion Criteria: At least 65 years of age who are eligible for the study vaccines; Who have given written informed consent at the time of enrollment); Those who are available for all the visits scheduled in the study; Subjects In good health as determined by medical history, physical examination and clinical judgment of the investigator Exclusion Criteria: History of egg allergy History of influenza vaccination in previous 6 months History of any pneumococcal vaccination Documented S. pneumonia infection in the previous 5 years Chemotherapy for malignancy within the past 30 days High-dose systemic steroid (prednisone ≥0.5 mg/kg/day) in the past 30 days Receipt of blood product within 6 months before enrollment Significant acute or chronic infection within the previous 7 days or fever within the previous day Any serious chronic or progressive disease Any condition that might interfere with the study results.
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Hee Jin Cheong, MD, PhD
    Organizational Affiliation
    Korea University Guro Hospital
    Official's Role
    Principal Investigator
    First Name & Middle Initial & Last Name & Degree
    Joon Young Song, MD, PhD
    Organizational Affiliation
    Korea University Guro Hospital
    Official's Role
    Study Director

    12. IPD Sharing Statement

    Citations:
    PubMed Identifier
    25980426
    Citation
    Song JY, Cheong HJ, Tsai TF, Chang HA, Choi MJ, Jeon JH, Kang SH, Jeong EJ, Noh JY, Kim WJ. Immunogenicity and safety of concomitant MF59-adjuvanted influenza vaccine and 23-valent pneumococcal polysaccharide vaccine administration in older adults. Vaccine. 2015 Aug 26;33(36):4647-52. doi: 10.1016/j.vaccine.2015.05.003. Epub 2015 May 14.
    Results Reference
    derived

    Learn more about this trial

    MF59-adjuvanted Influenza Vaccine and 23-valent Pneumococcal Polysaccharide Vaccine

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