drugset / Trial / NCT00161850
FSME IMMUN NEW Follow-up to Study 199 in Children Aged 1 to 6 Years
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Tick-Borne Encephalitis (TBE) Vaccine (Inactivated) | Vaccine | — | — |