CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 805 enrolled
Drug / intervention
1 dose of Meningococcal (group B) multicomponent recombinant adsorbed vaccine +1 morebiological
Likely dose
1 dose of Meningococcal (group B) multicomponent recombinant adsorbed vaccine 0.5 mLfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT01717638
NCT01717638Phase 3Completed

A Phase 3, Open Label, Multi-Center, Extension Study to Assess Antibody Persistence and Response to a Third or Fifth Dose of Novartis Meningococcal B Recombinant Vaccine in 4-Year-Old Children Who Previously Participated in Study V72P12E1

Novartis Vaccines·interventional·Posted Oct 30, 2012·Updated Jan 13, 2015

In Brief

A Phase 3 clinical trial evaluating 1 dose of Meningococcal (group B) multicomponent recombinant adsorbed vaccine and 2 doses of Meningococcal (group B) multicomponent recombinant adsorbed vaccine for Meningococcal Disease and Meningococcal Meningitis. Completed, enrolled 805 participants across 29 sites in 4 countries.

Detailed Summary

It is a Phase 3 extension of study V72P12E1 (NCT00944034). The main aim of the second extension study is to explore the bactericidal antibody persistence in 4-year-old children after a fourth dose boost of rMenB+OMV NZ or after a two-dose catch-up schedule of rMenB+OMV NZ administered to toddlers as part of their respective vaccination courses in study V72P12E1. In addition, this study will characterize the antibody response to a fifth dose boost in all children who received a three-dose primary series of rMenB+OMV NZ at 2, 3, 4 months of age (in parent study V72P12, NCT00721396), and only in a subset of children who received a three-dose primary series of rMenB+OMV NZ at 2, 4, 6 months of age (in parent study V72P12). Antibody response will also be characterized to a third dose boost of rMenB+OMV NZ administered at approximately 4 years of age in all children who received a two catch-up doses of rMenB+OMV NZ as toddlers in study V72P12E1. Finally, the safety and immunogenicity of two catch-up doses of rMenB+OMV NZ administered 2 months apart to healthy naïve children at 4 years of age will be assessed.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesCzechia, Italy, Spain, United Kingdom
Collaborators--

Timeline

Phase 3CompletedFinished
20132014201520162017201820192020202120222023202420252026
First PostedOct 30, 2012
Enrollment StartNov 1, 2012
Primary CompletionSep 1, 2013
Study CompletionOct 1, 2013
TodayJul 2, 2026
Enrollment to primary: 10 monthsPosted 13.7 years ago

Interventions

1 dose of Meningococcal (group B) multicomponent recombinant adsorbed vaccinebiological

0.5 mL of Meningococcal (group B) multicomponent recombinant adsorbed vaccine, Intramuscular, single dose

2 doses of Meningococcal (group B) multicomponent recombinant adsorbed vaccinebiological

0.5 mL of Meningococcal (group B) multicomponent recombinant adsorbed vaccine, Intramuscular, two doses, two months apart