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
| Type | Name | Description |
|---|---|---|
| OTHER | Blood draw | Annual 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.