drugset / Trial / NCT00578175

Immunogenicity and Safety of GlaxoSmithKline Biologicals' MMRV Vaccine vs. ProQuad® in Children 12-14 Months of Age

NCT00578175 ↗

Phase 2 Completed 1851 enrolled GlaxoSmithKline
RandomizedParallel-groupDouble-blindPrevention

Summary

The purpose of this observer blinded study is to provide information on vaccine immunogenicity and reactogenicity in comparison with the US standard of care (ProQuad®) when administered with Hepatitis A vaccine and Pneumococcal vaccine.

Timeline

Start
2007-11-20
Primary completion
2009-02-24
Completion
2009-03-17

Drugs

EvaluationDrugModalityDoseRoute
Subject Priorix-Tetra Vaccine — Subcutaneous
Comparator ProQuad Vaccine — Subcutaneous
Background Havrix Vaccine — Intramuscular
Background Prevnar Vaccine — Intramuscular