TBE Antibody Persistence and Booster Vaccination Study in Adults (Follow-up to Study 223)

Pfizer

Status and phase

Completed

Phase 4

Conditions

Encephalitis, Tick-Borne

Treatments

Biological: Tick-Borne Encephalitis (TBE) Vaccine (Inactivated)

Study type

Interventional

Funder types

Industry

Identifiers

NCT00503529

690701

EUDRACT # 2007-000440-27

Details and patient eligibility

About

The purpose of this study is to assess:

TBE antibody persistence 24, 34, 46 and 58 months (as applicable) after the first booster TBE vaccination with FSME-IMMUN 0.5ml given in Study 223, by means of ELISA (IMMUNOZYM FSME IgG) and Neutralization test (NT),
TBE antibody response to a second booster vaccination with FSME-IMMUN 0.5ml in the present study, by means of ELISA and NT,
Safety of FSME-IMMUN 0.5ml after the second booster vaccination.

Enrollment

314 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Subjects who participated in Study 223 will be eligible for participation in this study if:
they understand the nature of the study, agree to its provisions and provide written informed consent
they received the first booster vaccination with FSME-IMMUN 0.5ml during the course of study 223
blood was drawn after their first booster vaccination in Study 223.

Exclusion criteria

Subjects will be excluded from participation in this study if they:

received any TBE vaccination since their first booster vaccination with FSME-IMMUN 0.5ml
have a history of infection with or vaccination against other flaviviruses (e.g. dengue fever, yellow fever, Japanese B-encephalitis) since their first booster vaccination with FSME-IMMUN 0.5ml
are known to be HIV positive (a special HIV test is not required for the purpose of the study) since their first booster vaccination with FSME-IMMUN 0.5ml
have a known or suspected problem with drug or alcohol abuse (> 4 liters wine / week or equivalent level of other alcoholic beverages).

Subjects will not be eligible for booster vaccination if they:

are not clinically healthy, (i. e. the physician would have reservations vaccinating with FSME-IMMUN 0.5ml outside the scope of a clinical trial)
suffer from a disease (e.g. autoimmune disease) or are undergoing a form of treatment (e.g. systemic corticosteroids) that can be expected to influence immunological functions
are females of childbearing potential and are pregnant or breastfeeding before the booster vaccination (positive pregnancy test result at the medical examination before the booster vaccination)
have shown an allergic reaction to one of the components of the vaccine since their first booster vaccination in Study 223
are simultaneously participating in another clinical trial including administration of an investigational product within six weeks prior to the booster vaccination until the end of the study
do not agree to keep a Subject Diary.
Subjects who meet the eligibility criteria, but have a febrile illness (body temperature >= 38.0°C, measured orally) at the scheduled time of vaccination, will not be vaccinated until their body temperature returns to normal.
Subjects who have been administered any vaccination within 2 weeks prior to the booster vaccination will not be vaccinated until an interval of two weeks has passed.
If subjects have received antipyretics within 4 hours prior to the scheduled time of vaccination, the vaccination should be performed at a later time.
If a subject had a tick-bite within 4 weeks of the scheduled booster vaccination, the vaccination shall be delayed such that an interval of 4 weeks has passed since the tick-bite in order to avoid any interference with diagnostic assays in the event of a TBE infection.
If a subject has donated blood or plasma or has received a blood transfusion or immunoglobulins within 4 weeks of the scheduled booster vaccination, the vaccination shall be delayed until an interval of 4 weeks has passed.