drugset / Trial / NCT01018732

A Study to Evaluate the Persistence and Immune Response to a Booster Dose of MenACWY

NCT01018732

Phase 2 Completed 155 enrolled Novartis Vaccines Novartis · collab
Non-randomizedParallel-groupOpen-labelPrevention

Summary

The primary objective is to evaluate the persistence of bactericidal antibodies in adolescent subjects who completed study V59P6 in which they received either Novartis Meningococcal (MenACWY) Conjugate Vaccine or Licensed polysaccharide Men ACWY vaccine (Menomune®). The study will also enroll age-matched subjects who have never received any other meningococcal vaccine (naïve subjects) to serve as an additional control group.

Timeline

Start
2010-01
Primary completion
2010-07
Completion
2010-07

Drugs

EvaluationDrugModalityDoseRoute
Subject Menveo Vaccine