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
About this trial
This is an interventional prevention trial for Influenza, Human
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.
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
NCT ID
NCT02225327
First Posted
August 22, 2014
Last Updated
August 26, 2014
Sponsor
Korea University Guro Hospital
Collaborators
Novartis
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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