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Understanding Immunity Persistence After Adolescent MenC Vaccination

A Study to Evaluate the Persistence of Antibody Seven Years After a Booster Dose of Either a Glycoconjugate or a Polysaccharide Vaccine Against Serogroup C Neisseria Meningitidis Given to Adolescents

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01459432
Enrollment
134
Registered
2011-10-25
Start date
2011-11-30
Completion date
Unknown
Last updated
2015-11-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Antibody Persistance After Booster Dose of Men C Vaccine

Brief summary

The main purpose of this study is to evaluate the duration of immunity after a booster dose of a MenC-CRM vaccine given to adolescents between 13 and 15 years of age. Does seroprotection persist beyond teenage years and into the early twenties? This is the age group which is most likely to carry the organism and to transmit it to other members of the population. If a booster dose of MenC vaccine given to adolescents does produce protective levels of antibody which persist into early adulthood, this would strengthen the case for such a booster to be added to the UK routine immunisation schedule, to reduce the risk of a resurgence of the disease in the future.

Interventions

OTHERVenepuncture and blood sample collection.

Venepuncture and blood sample collection.

Sponsors

University of Oxford
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
20 Years to 23 Years
Healthy volunteers
Yes

Inclusion criteria

* Participants who completed clinical study M14P2E1 * Participant who are willing to participate and who would be expected to comply with the requirements of the protocol * Participants who have given informed consent for participation in the study

Exclusion criteria

* History of invasive meningococcal C disease (or any case of invasive meningococcal disease where the serotype was unknown) * Confirmed or suspected immunosuppressive or immunodeficient conditions, including human immunodeficiency virus (HIV) infection * Severe blood clotting disorders

Design outcomes

Primary

MeasureTime frame
Percentage of participants with rSBA titre ≥1:8 (correlate of protection).4 months

Secondary

MeasureTime frame
Geometric mean titre (GMT) rSBA.4 months

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 10, 2026