drugset / Trial / NCT00503529

TBE Antibody Persistence and Booster Vaccination Study in Adults (Follow-up to Study 223)

NCT00503529 ↗

Phase 4 Completed 314 enrolled Pfizer
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

EvaluationDrugModalityDoseRoute
Subject FSME-IMMUN Vaccine 0.5 ml Intramuscular