Baby Vaccine Study (Sched3)

Infectious Diseases Clinical Trial

Official title:

Assessment of Post Booster Antibody Responses in UK Infants Given a Reduced Priming Schedule of Meningococcal Serogroup B and 13 Valent Pneumococcal Conjugate Vaccines

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02482636
• Other study ID #: OVG2015/03
• Status: Completed
• Phase: Phase 2
• Start date: August 2015
• Est. completion date: June 2021

Study information

• Verified date: September 2021
• Source: University of Oxford
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This multicentre, parallel group, block randomised clinical trial aims to investigate the post booster antibody response in UK infants given a reduced priming schedule of meningococcal serogroup B vaccine and 13 valent pneumococcal conjugate vaccine. It will provide information about how best to include the meningococcal B vaccine (likely to be introduced late 2015) into the routine immunisation schedule. The UK Department of Health provides a routine vaccination schedule for children in the UK and are advised by the Joint Committee on Vaccination and Immunisation (JCVI). The Department of Health have announced that the meningococcal B vaccine (Bexsero) be introduced to the routine schedule as a 2+1 schedule. Cost effectiveness could also be improved by removing the current MenC conjugate vaccine dose given at 3 months of age. There is no published immunogenicity data for Bexsero when given at 2, 4 and 12 months of age (2+1 schedule) and with concomitant Infanrix/IPV/Hib which has now replaced Pediacel in the infant programme. This change to the schedule would result in three injections at 2, 4 and 12 months, and given previous reluctance among parents for three injections at one visit, an option to reduce PCV13 to a 1+1 schedule (priming dose at 3 months and booster at 12 months) will be assessed in this study.

Description:

The study's primary objective is to assess antibody response to the pneumococcal vaccine after the final infant vaccinations at approximately 13 months of age, and secondary objectives include antibody response following meningococcal B and C vaccines, tetanus, diphtheria and pertussis vaccines. In addition, the effect of maternal pertussis vaccination in pregnancy on infant immune response to vaccines, the prevalence of carriage of pneumococcal serotypes at 12 and 18 months of age and reactogenecity following each vaccine will be assessed. 200 healthy children who have not yet received their routine infant immunisations will be enrolled between 8 and 12 weeks old. Participants will be randomised into one of two groups with differing vaccine schedules. Children in both groups will receive their routine immunisations with the following changes: the addition of 3 doses of a meningococcal B vaccine at 2, 4 and 12 months and a meningococcal C vaccine at 12 months only (instead of a dose at 3 and 12 months). The 2 groups will differ by the number of doses of the 13-valent pneumococcal vaccine (PCV13); to be given either at 2, 4, and 12 months of age (as currently given in the routine schedule) or at 3 and 12 months of age. Each participant will have 2 blood tests: at 5 and 13 months of age, and 2 nose swabs: at 12 and 18 months of age to address the objectives of the study. Parents will be asked to complete a health diary to record any adverse events in the 7 days following vaccinations and a continuous thermometer (ibutton) will be used to record the temperature for 24 hours after each vaccination. If the blood samples at 13 months reveal antibody titres that are below the level indicative of protection, a recommendation will be made for booster vaccinations.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 189
• Est. completion date: June 2021
• Est. primary completion date: November 1, 2017
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 8 Weeks to 12 Weeks

Eligibility

Inclusion Criteria:

• Infants due to receive their primary immunisations , aged up to 13 weeks on first vaccinations.
• Written informed consent given by mother who is aged >= 16 years [NB mother is preferable as consent also allows permission to record the date of pertussis immunisation in pregnancy, which may need to be verified in her medical record. Where mother is not available, consent may be taken from father or legal guardian and maternal pertussis status noted as not known]

Exclusion Criteria:

• Bleeding disorder
• Fulfil any of the contraindications to vaccination as specified in The Green Book [https://www.gov.uk/government/organisations/public-health-england/series/immunisation

-against-infectious-disease-the-green-book]:

• At risk of invasive pneumococcal disease (IPD) as defined in the Green Book pneumococcal chapter and those born prior to 37 weeks gestation
• Confirmed anaphylactic reaction to a previous dose of the vaccine, or
• Confirmed anaphylactic reaction to any constituent or excipient of the vaccine(s).
• A confirmed anaphylactic reaction to neomycin, streptomycin or polymyxin B (which may be present in trace amounts in the tetanus vaccine) and/or kanamycin, histidine, sodium chloride or sucrose (which may be present in trace amounts in the MenB vaccine).
• Latex hypersensitivity (the syringe cap of Bexsero may contain natural rubber latex)

Related Conditions & MeSH terms

• Communicable Diseases
• Infections
• Infectious Diseases

Intervention

Biological:
• DTaP/IPV/Hib vaccine
Given at 2, 3 and 4 months to Group 1 and 2
• 13 valent Pneumococcal Conjugate Vaccine
Given at 2,4 and 12 months in group 1, given at 3 and 12 months in group 2
• Rotavirus vaccine
Given at 2 and 3 months to Group 1 and 2
• 4-component Meningococcal B vaccine
Given at 2, 4 and 12 months to Group 1 and 2
• Meningococcal C/Hib vaccine (MenC/Hib vaccine)
Given at 12 months to Group1 and 2
• Measles/Mumps/Rubella Vaccine (MMR vaccine)
Given at 13 months to Groups 1 and 2

Locations

Country	Name	City	State
United Kingdom	Centre for Clinical Vaccinology and Tropical Medicine	Oxford	Oxfordshire

Sponsors (3)

Lead Sponsor	Collaborator
University of Oxford	Public Health England, University College, London

Country where clinical trial is conducted

United Kingdom, 

References & Publications (1)

Goldblatt D, Southern J, Andrews NJ, Burbidge P, Partington J, Roalfe L, Valente Pinto M, Thalasselis V, Plested E, Richardson H, Snape MD, Miller E. Pneumococcal conjugate vaccine 13 delivered as one primary and one booster dose (1 + 1) compared with two primary doses and a booster (2 + 1) in UK infants: a multicentre, parallel group randomised controlled trial. Lancet Infect Dis. 2018 Feb;18(2):171-179. doi: 10.1016/S1473-3099(17)30654-0. Epub 2017 Nov 22. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Pneumococcal serotype specific geometric mean concentrations (GMCs) in blood samples following the completion of either a 2, 4 and 12 month schedule of PCV13 vaccination, or only 3 and 12 month PCV13 vaccination	pneumococcal IgG concentration for the 13 serotypes contained in the vaccine	Blood samples collected at 13 months of age
Secondary	13 serotype-specific pneumococcal IgG GMCs and functional pneumococcal antibodies and proportions greater than or equal to =0.35µg/mL for each serotype in blood samples taken at 5 and 13 months		blood samples taken at 5 and 13 months
Secondary	Titres and proportions of participants achieving antibody responses to MenB vaccination human Serum Bactericidal Antibody (SBA) titres =4 for the three main vaccine antigen target MenB strains, 5/99 (NadA), NZ98/254 (PorA) and 44/76-SL (fHbp)		Blood samples taken at 5 months
Secondary	Meningococcal serogroup C human SBA geometric mean titres (GMTs) and proportion of infants =4 (5 month blood only); rabbit SBA titres (GMT) and proportion of infants with titres 8 and 128 (13 month blood only)		blood samples taken at 5 months and 13 months
Secondary	Meningococcal serogroup W hSBA GMTs and proportion of infants with titre =4 at 5 and 13 months of age		blood samples taken at 5 and 13 months
Secondary	GMC of anti-PRP IgG [Hib antigen] and proportion of infants with concentrations of > 0.15µg/mL and 1.0µg/mL in the blood samples taken at 5 and 13 months of age		Blood samples taken at 5 and 13 months of age
Secondary	GMC of IgG to pertussis antigens (PT, PRN, FHA and FIM 2 and 3) in the blood samples taken at 5 months of age		Blood samples taken at 5 months of age
Secondary	GMC of anti-tetanus toxoid IgG and proportions =0.1 IU/mL and =1.0 IU/mL in the blood samples taken at 5 months of age		Blood samples taken at 5 months of age
Secondary	GMC of anti-diphtheria toxoid IgG and proportions =0.1IU/mL and =1.0 IU/mL in the blood samples taken at 5 months of age		blood samples taken at 5 months of age
Secondary	Frequency of carriage of identified pneumococcal serotypes from the nasal swab collected prior to the booster vaccinations at 12 months of age and six months later		Nasal swab taken at 12 months and 18 months
Secondary	Number of participants with local adverse events at injection site and temperature as recorded in the daily health diary for the week following vaccination and any systemic symptoms. Temperature also recorded and analysed from the iButton system		Measurements following vaccinations at 2, 3, 4, 12 and 13 months of age

External Links

•   Immunogenicity of the UK group B meningococcal vaccine (4CMenB) schedule against groups B and C meningococcal strains (Sched3): outcomes of a multicentre, open-label, randomised controlled trial
•   Pneumococcal conjugate vaccine 13 delivered as one primary and one booster dose (1 + 1) compared with two primary doses and a booster (2 + 1) in UK infants: a multicentre, parallel group randomised controlled trial