Clinical Trials Directory

Trials / Completed

CompletedNCT00452621

Evaluation of Long-Term Immunogenicity in Children and Adolescents Boosted With a New Pediatric TBE Vaccine After Five Years

A Phase IV, Uncontrolled, Open-Label, Multi-Center Study in Children and Adolescents: Evaluation of Long-Term Immunogenicity in Subjects Boosted With a New Pediatric TBE Vaccine (Free of Protein-Derived Stabilizer) in Study V48P4E1, Five Years After First Booster Immunization

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
235 (estimated)
Sponsor
Novartis · Industry
Sex
All
Age
6 Years – 16 Years
Healthy volunteers
Accepted

Summary

blood draw five years after booster-immunization with TBE vaccine to investigate immunogenicity in children

Conditions

Interventions

TypeNameDescription
PROCEDUREblood draw

Timeline

Start date
2007-02-01
First posted
2007-03-27
Last updated
2008-04-23

Locations

8 sites across 1 country: Germany

Source: ClinicalTrials.gov record NCT00452621. Inclusion in this directory is not an endorsement.