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

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Novartis

Status and phase

Completed
Phase 4

Conditions

Encephalitis, Tick-Borne

Treatments

Biological: Tick-Borne Encephalitis vaccine

Study type

Interventional

Funder types

Industry

Identifiers

NCT00311493
V48P2E3
498

Details and patient eligibility

About

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

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Healthy volunteers of both sexes aged >18 who participated in another study on TBE vaccination

Exclusion criteria

  • Subjects with any condition, in the opinion of the Investigator, might interfere with the evaluation of the study objectives.

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Factorial Assignment

Masking

None (Open label)

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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