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Specific B-cell Memory After a Single Dose or Booster MenC Conjugate Vaccination: a Pilot Study in Adults - B-cell Memory After MenC Vaccination

Specific B-cell Memory After a Single Dose or Booster MenC Conjugate Vaccination: a Pilot Study in Adults - B-cell Memory After MenC Vaccination

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
EU CTR
Registry ID
EUCTR2006-002358-31-NL
Enrollment
20
Registered
2006-05-17
Start date
2006-09-11
Completion date
Unknown
Last updated
2022-04-04

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

Conditions

Bacterial meningitis is caused by several pathogens such as Hib, Streptococcus pneumoniae and MenC. A MenC conjugate vaccination was introduced into the National Vaccination Program at the age of 14 months in 2002. In the following years it will become clear how effective MenC vaccination is in the long term. Long term protection is based on memory after vaccination or natural infection. In the Netherlands MenC memory is induced by a single vaccination.

Interventions

Trade Name: NeisVac-C Pharmaceutical Form: Trade Name: Meningovax A+C Pharmaceutical Form:

Sponsors

RIVM
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Participants have to fulfil all of the following criteria, and will be screened for these after signing the informed consent: - Good general health; - Provision of written informed consent; - Adherent to protocol, and available during the study period. Are the trial subjects under 18? no Number of subjects for this age range: F.1.2 Adults (18-64 years) yes F.1.2.1 Number of subjects for this age range F.1.3 Elderly (>=65 years) F.1.3.1 Number of subjects for this age range

Exclusion criteria

Exclusion criteria: Any of the following criteria will exclude a volunteer from participation, at the start of the study: - Severe acute (infectious) illness of fever (>38.5°C) within 2 weeks before vaccination; - Present evidence of serious disease(s) demanding medical treatment that might interfere the results of the study; - Known or suspected allergy to any of the vaccine components (by medical history); - Known or suspected immune deficiency; - History of any neurologic disorder, including epilepsy; - Previous administration of plasma products (including immunoglobulins) within the last 6 months; - Pregnancy.

Design outcomes

Primary

MeasureTime frame
Main Objective: How long does B-cell memory persist after a single conjugate MenC vaccination in adults and which cells are involved?;Secondary Objective: How is this related to the age of first vaccination? And how to define correlates of protection for immunity and memory after MenC conjugate vaccination?;Primary end point(s): Characterization of the memory B-cell response after MenC (conjugate) vaccination, using Luminex bead based array technology, serum bactericidal antibody assay (SBA), FACS analysis and ELISPOT assay.

Countries

Netherlands

Outcome results

None listed

Source: EU CTR (via WHO ICTRP) · Data processed: Feb 4, 2026