Evaluation of Long-Term Immunogenicity in Subjects Boosted With a TBE Vaccine for Adults

NCT00311493 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 179

Last updated 2007-03-13

No results posted yet for this study

Summary

The purpose of this study it is to evalutate the persistence of antibodies after a booster immunisation with a TBE vaccine for adults

Conditions

  • Encephalitis, Tick-Borne

Interventions

BIOLOGICAL

Tick-Borne Encephalitis vaccine

Sponsors & Collaborators

  • Novartis Vaccines

    collaborator INDUSTRY
  • Novartis

    lead INDUSTRY

Principal Investigators

  • Drug Information Services · Chiron Corporation

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Model
FACTORIAL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2006-02-28

Countries

  • Germany

Study Locations

More Related Trials

Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00311493 on ClinicalTrials.gov