CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 818 enrolled
Drug / intervention
Nimenrix +1 morebiological
Likely dose
Not stated in 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/NCT00715910
NCT00715910Phase 2Completed

Long-term Antibody Persistence of GSK Biologicals' MenACWY-TT Vaccine Versus Menactra® in Healthy Adolescents/Adults Aged 10-25 Years and Booster Response to MenACWY-TT Vaccine Administered at 5 Years Post-primary Vaccination

GlaxoSmithKline·interventional·Posted Jul 15, 2008·Updated Nov 27, 2014

In Brief

A Phase 2 clinical trial evaluating Nimenrix and Blood sampling for Infections, Meningococcal. Completed, enrolled 818 participants across 10 sites.

Detailed Summary

In this study, the concentration of antibody to the vaccine one year, three and five years after vaccination in subjects who were vaccinated with GSK Biologicals' meningococcal vaccine GSK134612 and Menactra® in a previous study (whose objectives \& outcome measures are presented in a separate protocol posting with NCT number =00454909) will be evaluated. The safety and immune response to a booster dose of vaccine GSK134612 administered at 5 years post-primary vaccination and a primary vaccination of a newly enrolled group with GSK 134612 vaccine will also be evaluated.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--

Timeline

Phase 2CompletedFinished
20082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedJul 15, 2008
Enrollment StartJul 1, 2008
Primary CompletionApr 1, 2013
Study CompletionOct 1, 2013
TodayJul 2, 2026
Enrollment to primary: 4.8 yearsPosted 18.0 years ago

Interventions

Nimenrixbiological

One dose, as intramuscular injection

Blood samplingprocedure

Blood samples will be collected from subjects 10-25 years of age as per enrollment in primary study and from subjects in the Nimerix Naive Group at Month 60 (Year 5) and 1 month post booster vaccination (Month 61).