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Response of United Kingdom (UK) Infants to a Reduced Primary Schedule With Meningococcal C and Pneumococcal Conjugate Vaccines

Response of United Kingdom (UK) Infants to a Reduced Primary Schedule With Meningococcal C and Pneumococcal Conjugate Vaccines

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00197808
Acronym
sched1
Enrollment
392
Registered
2005-09-20
Start date
2005-04-30
Completion date
2010-01-31
Last updated
2020-10-01

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

Conditions

Pneumococcal Infections, Meningococcal Infections

Keywords

Streptococcus pneumoniae, Neisseria meningitidis

Brief summary

The purpose of the study is to evaluate the immune responses of UK infants after one or two doses of pneumococcal conjugate vaccine or one or two doses of three different types of meningococcal conjugate vaccine given at either two and three or two and four months of age.

Interventions

BIOLOGICALmenjugate

men C conjugate vaccine

BIOLOGICALMen C conjugate vaccine

men C conjugate vaccine

BIOLOGICALMen C conjugate

men C conjugate vaccine

BIOLOGICALMen C Conjugate

men C conjugate vaccine

Sponsors

Public Health England
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
7 Weeks to 11 Weeks
Healthy volunteers
Yes

Inclusion criteria

* Written informed consent obtained from parent or legal guardian of infant * Age 7-11 weeks at first dose

Exclusion criteria

* Any contraindications to vaccination as specified in the UK Handbook Immunisation Against Infectious Disease (Ed 1996) * \< 7 weeks or \> 11 weeks at first dose

Design outcomes

Primary

MeasureTime frameDescription
Immunogenicity3 months after last sampleSBA men C responses

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 31, 2026