drugset / Trial / NCT04648241

Study to Evaluate the Immunogenicity, Safety, and Tolerability of a Tick-Borne Encephalitis (TBE) Vaccine in Healthy Japanese Participants 1 Year of Age and Older

NCT04648241 ↗

Phase 3 Completed 165 enrolled Pfizer
Non-randomizedParallel-groupOpen-labelPrevention

Summary

The main purpose of this study is to provide safety and immunogenicity data in Japanese participants.

Timeline

Start
2021-01-18
Primary completion
2022-02-21
Completion
2022-02-21

Drugs

EvaluationDrugModalityDoseRoute
Subject TBE vaccine Vaccine 0.25 ml Intramuscular
Subject TBE vaccine Vaccine 0.5 ml Intramuscular