drugset / Trial / NCT06825312

Immunogenicity, Safety, and Antibody Persistence of Different Immunization Strategies Against Japanese Encephalitis

NCT06825312

RandomizedParallel-groupOpen-labelPrevention

Summary

The main objective of this study is to evaluate the persistence of Japanese encephalitis antibodies in participants at the age of 6, after they have followed different Japanese encephalitis vaccination schedules. Furthermore, the study will assess the immunogenicity and antibody persistence of primary immunization across different Japanese encephalitis vaccination schedules, as well as the immunogenicity following booster immunizations within these schedules. The safety of each vaccine dose will also be evaluated.

Timeline

Start
2023-11-11
Primary completion
2030-12-31
Completion
2031-12-31

Drugs

EvaluationDrugModalityDoseRoute
Subject IC51 Vaccine 0.5 ml Subcutaneous
Subject Japanese Encephalitis Vaccine (Vero Cell), Inactivated Vaccine 0.5 ml Intramuscular

Indications