Tick-Borne Encephalitis Clinical Trial
Official title:
Phase 1 Study of the Safety and Immunogenicity of Tick-Borne Langat/Dengue 4 Chimera (LGT(TP21)/DEN4), a Live Attenuated Vaccine for Tick-Borne Encephalitis
Tick-borne encephalitis (TBE) is a viral illness common in the Northern Hemisphere, especially Europe and Asia. TBE infection may lead to central nervous system problems and death. The purpose of this study is to test the safety of and immune response to a TBE vaccine in healthy adults. The vaccine is related to a live attenuated virus developed against dengue virus infection.
TBE is a common illness in Europe and Asia, where it is usually associated with mild illness
but sometimes leads to long-term symptoms and even death. This study will evaluate the
safety and immunogenicity of a live attenuated chimeric virus, LGT(TP21)/DEN4, which is
derived from the Langat flavivirus and DEN4 dengue virus serotypes.
Each volunteer will be involved in the study for 180 days. Participants in Cohort 1 will be
randomly assigned to receive LGT(TP21)/DEN4 or placebo at study entry. Cohort 2 will begin
only after safety review of all participants in Cohort 1. Participants in Cohort 2 will
receive a higher dose of LGT(TP21)/DEN4 or placebo.
After vaccination, participants will be asked to monitor their temperatures every day for 16
days and on Day 19. Study visits will occur every other day after vaccination until Day 16,
followed by 5 additional visits at selected days through Day 180. Blood collection and a
targeted physical exam will occur at each study visit. Some participants will be asked to
undergo a skin biopsy or additional blood collection at selected visits.
;
Allocation: Randomized, Endpoint Classification: Safety Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator), Primary Purpose: Prevention
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