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Clinical Trial Summary

The aim of this study is to investigate the immunogenicity response in adults up to 10 years after one booster dose. Data collected from this study will allow for greater information to prescribers who administer TBE vaccine, so that they can appropriately time the administration of booster vaccinations to individuals who received different vaccination schedules and who live in tick borne encephalitis endemic regions.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01562444
Study type Interventional
Source GlaxoSmithKline
Contact
Status Completed
Phase Phase 4
Start date March 8, 2012
Completion date September 30, 2016

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