CompletedNCT00163618
Study to Investigate the Seropersistence of TBE Virus Antibodies Approx. 3 Years After a Booster Vaccination With FSME-IMMUN 0.25 mL JUNIOR in Children
Studying Encephalitis
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Pfizer
- Principal Investigator
- Baxter BioScience InvestigatorBaxter Healthcare Corporation
- Intervention
- Formaldehyde inactivated, sucrose gradient purified TBE virus antigen, strain Neudörfl(biological)
- Eligibility
- 7-11 years · All sexes
- Timeline
- 2005 – 2006
Study locations (4)
- Bahnhofstraße 9, Hermagor, Austria
- Freistädter Strasse 290, Linz, Austria
- Conrad-von-Hoetzendorf-Strasse, Voitsberg, Austria
- Grieskirchner Strasse 17, Wels, Austria
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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