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Clinical Trial Summary

Immunogenicity, Safety, Tolerability and Ability to Prime for Memory of Meningococcal C Conjugate Vaccine in healthy children


Clinical Trial Description

The aim of this study is to investigate the immunogenicity offered by MenCC vaccine when administered in different schedules at different years of life: 2 doses in the first year of life given 2 months apart (at 2 and 4 months of age), with a booster in the second year of life, or 1 dose in the first year of life (at 2 or 6 months of age), with a booster in the second year of life, or only 1 dose in the second year of life. ;


Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Prevention


Related Conditions & MeSH terms


NCT number NCT00311415
Study type Interventional
Source Novartis
Contact
Status Completed
Phase Phase 3
Start date October 2005
Completion date April 2008

See also
  Status Clinical Trial Phase
Completed NCT00310674 - Immunogenicity, Safety and Tolerability, of Chiron Meningococcal C Conjugate Vaccine Administered to Healthy Premature and Non Premature Children of 3 Months of Age Phase 3
Completed NCT00310687 - Persistence of Immune Response After Vaccination With MCC Phase 4
Completed NCT00310700 - Kinetics of B Cell Response in Infants Menjugate Vaccination Phase 4
Completed NCT00316654 - Persistence of Antibody Response to N. Meningitidis Group C in Children Phase 4
Completed NCT00310713 - Persistence of Antibodies and Kinetics of B Cell Response in Healthy Children After Vaccination With MCC Vaccine Phase 4