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Clinical Trial Summary

The primary objectives of this study are to evaluate the immunogenicity and safety of concomitant administration of V419 (PR51) with 2 types of meningococcal serogroup C conjugate (MCC) vaccines to healthy infants at 3 and 4 months of age in terms of antibody seroprotection rate (SPR) to MCC. Participants also received a Haemophilus influenza type B (Hib)-MCC vaccination at 12 months of age. It was hypothesized that the SPR to MCC at 1 month post-dose 2 of either tetanus toxoid conjugated Meningo C (MCC-TT) or CRM197 conjugated Meningo C (MCC-CRM) vaccines would be acceptable when administered concomitantly with V419.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01553279
Study type Interventional
Source MCM Vaccines B.V.
Contact
Status Completed
Phase Phase 3
Start date March 30, 2012
Completion date September 27, 2013

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