Understanding the Persistence of Immunity After MenC Vaccines
An Observational Study Into the Maintenance of Seroprotection Against Meningococcal Serogroup C Disease Throughout Childhood Following a Single Dose of a Conjugated Meningococcal Serogroup C Vaccine Administered to Toddlers
1 other identifier
observational
240
1 country
1
Brief Summary
Neisseria meningitidis occurs worldwide as endemic disease1 and is a major cause of invasive infections such as meningitis and septicaemia. Three protein-polysaccharide conjugate serogroup C meningococcal (MenC) vaccines were developed in the late 1990's and an accelerated programme of clinical trials in the UK led to licensure of these MenC vaccines in 1999 and these vaccines were introduced into the routine infant immunisation schedule at 2, 3 and 4 months. However, children who were aged 1-18 years in 2000 only received a single dose of a MenC conjugate vaccine during the mass immunisation campaign. Previous studies have demonstrated rapid waning of MenC specific antibody concentrations and serum bactericidal antibody (SBA) titres following immunisation in young children. A cross-sectional review on rates of sero-protection against MenC disease in the UK has demonstrated that the majority of children who were immunised with a single dose of a MenC conjugate vaccine between the ages of 1-10 did not have protective titres of MenC SBA 7 years after the immunisation campaign. As this cohort of children reaches adolescence there is a risk of increased transmission of the organism and a resurgence of meningococcal disease in children who do not have protective levels of antibody. There is thus a need to conduct a study evaluating the changes in MenC SBA titres over time in children who received a single dose of a MenC vaccine in early childhood which is the main objective of this study.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Jun 2010
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
May 18, 2010
CompletedFirst Posted
Study publicly available on registry
May 20, 2010
CompletedStudy Start
First participant enrolled
June 1, 2010
CompletedPrimary Completion
Last participant's last visit for primary outcome
November 1, 2010
CompletedStudy Completion
Last participant's last visit for all outcomes
November 1, 2010
CompletedMay 9, 2013
May 1, 2013
5 months
May 18, 2010
May 7, 2013
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Percentage of participants with rSBA titres >1:8 (correlate of protection)
6 months
Secondary Outcomes (2)
MenC rSBA GMTs at all time points when sera is available after receiving a dose of MenC vaccine
6 months
Percentage of children at each time point with MenC SBA titres >1:8
6 months
Study Arms (1)
MenC vaccinated healthy children
Children who received a single dose of a MenC conjugate vaccine at age 1-3 years 10 years earlier.
Interventions
1. Venepuncture and blood sample collection in 2010 in a sample of children who received a single dose of a MenC conjugate vaccine at age 1-3 years 10 years earlier. 2. A booster dose of a MenC conjugate vaccine (optional).
Eligibility Criteria
Healthy children who participated in the U01-Td5I-303/ C01.183 study from 2001 to 2007 who will be aged 11 to 13 years in 2010, all of whom would have received a single dose of a MenC conjugate vaccine in 2000 as part of the nationwide immunisation campaign.
You may qualify if:
- Participant whose parent is willing and able to give informed consent for participation in the study.
- Participant who gives assent for participation in the study.
- Male or Female, aged 11 to 13 years.
- Known to be free from medical problems as determined by a medical history and clinical assessment
- Participated in the University of Oxford clinical trial: U01-Td5I-303/ C01.183
You may not qualify if:
- History of invasive meningococcal C disease
- Any vaccination against MenC disease with the exception of a single dose in 2000 during the nationwide MenC immunisation campaign
- Confirmed or suspected immunosuppressive or immunodeficient conditions, including human immunodeficiency virus (HIV) infection.
- Major congenital defects or serious chronic illness
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Oxford Vaccine Group, University of Oxford
Oxford, OX3 7LJ, United Kingdom
Related Publications (1)
Khatami A, Peters A, Robinson H, Williams N, Thompson A, Findlow H, Pollard AJ, Snape MD. Maintenance of immune response throughout childhood following serogroup C meningococcal conjugate vaccination in early childhood. Clin Vaccine Immunol. 2011 Dec;18(12):2038-42. doi: 10.1128/CVI.05354-11. Epub 2011 Oct 28.
PMID: 22038849BACKGROUND
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Matthew Snape
University of Oxford
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
Study Record Dates
First Submitted
May 18, 2010
First Posted
May 20, 2010
Study Start
June 1, 2010
Primary Completion
November 1, 2010
Study Completion
November 1, 2010
Last Updated
May 9, 2013
Record last verified: 2013-05