drugset / Trial / NCT00161889

FSME IMMUN NEW Follow-up to Study 205 in Children Aged 6 to 16 Years

NCT00161889 ↗

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 volunteers who completed two vaccinations in one of the three treatment groups of Baxter study 205 (safety and immunogenicity of two vaccinations with FSME IMMUN NEW in healthy volunteers aged 6 to 16 years).

Timeline

Start
2002-02
Primary completion
—
Completion
2002-08

Drugs

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