Clinical Trials Directory

Trials / Completed

CompletedNCT01562444

Study to Evaluate Long Term Immunogenicity up to 10 Years After the First Booster Immunization With Tick Borne Encephalitis Vaccine in Adults Who Received 1 of 3 Different Primary Vaccination Schedules

A Phase IV, Open-label, Single-center Study to Evaluate Long Term Immunogenicity up to 10 Years After the First Booster Immunization With Tick Borne Encephalitis Vaccine in Adults Who Received 1 of 3 Different Primary Vaccination Schedules

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
206 (actual)
Sponsor
GlaxoSmithKline · Industry
Sex
All
Age
18 Years
Healthy volunteers
Accepted

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.

Conditions

Interventions

TypeNameDescription
OTHERBlood drawAnnual blood draw at years 6 (Visit 18), 7 (Visit 19), 8 (Visit 20), 9 (Visit 21) and 10 (Visit 22)

Timeline

Start date
2012-03-08
Primary completion
2016-09-30
Completion
2016-09-30
First posted
2012-03-23
Last updated
2021-08-12
Results posted
2018-08-31

Locations

1 site across 1 country: Czechia

Source: ClinicalTrials.gov record NCT01562444. Inclusion in this directory is not an endorsement.