drugset / Trial / NCT00161850

FSME IMMUN NEW Follow-up to Study 199 in Children Aged 1 to 6 Years

NCT00161850 ↗

Phase 2 Completed 615 enrolled Pfizer
RandomizedParallel-groupDouble-blind

Summary

The purpose of this study is to investigate the safety and immunogenicity of the third vaccination with one of three different concentrations of a TBE vaccine in all subjects who completed two vaccinations in one of the three treatment groups of Baxter study 199 (a dose-finding study to investigate the safety and immunogenicity of two vaccinations with FSME IMMUN NEW in healthy subjects aged 1 to 6 years).

Timeline

Start
2002-02
Primary completion
—
Completion
2002-08

Drugs

EvaluationDrugModalityDoseRoute
Subject Tick-Borne Encephalitis (TBE) Vaccine (Inactivated) Vaccine — —