drugset / Trial / NCT00503529
TBE Antibody Persistence and Booster Vaccination Study in Adults (Follow-up to Study 223)
Non-randomizedSingle-groupOpen-labelPrevention
Summary
The purpose of this study is to assess: * TBE antibody persistence 24, 34, 46 and 58 months (as applicable) after the first booster TBE vaccination with FSME-IMMUN 0.5ml given in Study 223, by means of ELISA (IMMUNOZYM FSME IgG) and Neutralization test (NT), * TBE antibody response to a second booster vaccination with FSME-IMMUN 0.5ml in the present study, by means of ELISA and NT, * Safety of FSME-IMMUN 0.5ml after the second booster vaccination.
Timeline
- Start
- 2007-07
- Primary completion
- 2010-07
- Completion
- 2010-09
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | FSME-IMMUN | Vaccine | 0.5 ml | Intramuscular |