Tdap Booster: An Immunogenicity and Safety Study of Tetanus, Diphtheria and Acellular Pertussis Vaccine Booster
Study Details
Study Description
Brief Summary
Open-label, randomized, multi-centre study in which 400 subjects, divided into two groups, will receive Td5ap or Td1aP as a single injection. We will then describe the immune response and safety profile of the combined vaccine booster.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
Phase 4 |
Detailed Description
The vaccines in the study are COVAXIS (Td5ap), Sanofi Pasteur Canada, and diTekiBooster (Td1aP), Statens Serum Institut, Denmark.
The primary objective of the study is to describe the immune response to diphtheria toxin, tetanus toxoid, pertussis toxin, filamentous haemagglutinin (FHA), fimbriae 2/3 and pertactin four weeks after immunization with Td1aP and Td5ap.
The secondary objectives include:
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describing the safety of a fith dose of DTP vaccines in 14-15 year-old children by observing systemic and local adverse reactions
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describing pre-booster antibody levels
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describing pre-booster and post-booster IgG and IgA levels in saliva
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describing in a subpopulation the pre-booster and post-booster T cell immune responses as determined by the production of cytokines
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describing in a subpopulation the pre-booster and post-booster B cell immune responses as determined by the number of effector and memory B-cells
The sample size is 400 subjects (200 in group 1 and 200 in group 2). It will be an open-label, randomized, multi-centre study in which group 1 will receive Td5ap as a single injection and group 2 will receive Td1aP as a single injection. DTP antibodies will be measured before and 28 days (+ 14 days) after Td5ap and Td1aP vaccination. The proportion of children with positive IgG antibody response will be measured in each study arm. Sera will be tested blindly by established ELISA methods and saliva samples will be analyzed by exploratory assays. In a subpopulation cellmediated immunity will be analyzed. The safety evaluation criteria will be the percentage of subjects with adverse events describing injection-site adverse reactions, systemic adverse events, daily temperatures and serious adverse events.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Active Comparator: Td5ap Group 1 receiving Td5ap as a single intramuscular injection. |
Biological: Td5ap
Intramuscular injection of 0.5 mL Td5ap (COVAXiS) on day 1.
Other Names:
|
| Active Comparator: Td1aP Group 2 receiving Td1aP as a single intramuscular injection |
Biological: Td1aP
Intramuscular injection of 0.5 mL Td1aP (diTekiBooster) on day 1.
Other Names:
|
Outcome Measures
Primary Outcome Measures
- to describe in each arm the immune response to diptheria toxin, tetanus toxoid, pertussis toxin, FHA, fimbriae 2/3 and pertactin four weeks after immunization with Td1aP and Td5ap [42 days]
Secondary Outcome Measures
- safety of a fith dose of DTP vaccines [42 days]
- pre-booster antibody levels [42 days]
- pre-booster and post-booster IgG and IgA levels [42 days]
- pre-booster and post-booster T cell immune responses [42 days]
- pre-booster and post-booster B cell immune responses [42 days]
Eligibility Criteria
Criteria
Inclusion Criteria:
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healthy subject
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14-15 years old
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eligible for their school-leaving booster for DTP
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received a complete primary vaccination with a 5-component acellular pertussis vaccine (DT5aP-IPV-Hib) at 3, 5 and 12 months of age and vaccinated with a 5-component acellular pertussis vaccine (Td5aP-IPV or Td5aP + IPV) as a booster at 5½ years of age
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informed consent form signed by the subject and parent(s)/legal representative
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subject understand and comply with the study procedures (i.e. able to read and write Swedish)
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female must provide an agreement that they are either sexually continent or practice adequate contraceptive methods (intra-uterine contraceptive device (IUCD), hormonal contraceptives, condoms or other adequate barrier contraception).
Exclusion Criteria:
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acute febrile illness or axillary temperature ≥38.0°C at the time of vaccination
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receipt of immunoglobulin within the previous 3 months, immunosuppression (e g evidence of impaired cell mediated immunity, receipt of immunosuppressant drugs within the previous 3 months or receipt of systemic corticosteroids given daily or on alternate days at ≥20 mg/day prednisone equivalent during >14 days within the past 30 days)
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receipt of a non-study vaccine in the past 30 days
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evolving encephalopathy not attributable to another identifiable cause within 7 days of administration of a previous dose of any vaccine
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booster vaccination with tetanus, low dose diphtheria and acellular pertussis vaccine since the booster vaccination at 5½ years of age
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previous clinical or bacteriological diagnosis of diphtheria, tetanus or pertussis
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hypersensitivity to any component of any of the study vaccines
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current participation in any other clinical trial or participation in any clinical trial in the previous month
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inability to adhere to the protocol, including plans to move from the area
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severe chronic disease
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family history of congenital or hereditary immunodeficiency
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any sever thrombocytopenia or any other coagulation disorder that would contraindicate intramuscular injection
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any medical condition, which in the opinion of the investigator, might interfere with the evaluation of the study objectives.
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Swedish Institute for Infectious Disease Control | Lund | Sweden | 221 85 |
Sponsors and Collaborators
- Swedish Institute for Infectious Disease Control
- MCM Vaccines B.V.
- Statens Serum Institut
Investigators
- Principal Investigator: Leif Gothefors, Prof. em., Swedish Institute for Infectious Disease Control
- Study Director: Eva Netterlid, Swedish Institute for Infectious Disease Control
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- 2008-008195-13