drugset / Trial / NCT02302066

Safety and Immunogenicity of Different Schedules of Takeda's Tetravalent Dengue Vaccine Candidate (TDV) in Healthy Participants

NCT02302066 ↗

Phase 2 Completed 1800 enrolled Takeda
RandomizedParallel-groupQuadruple-blindPrevention

Summary

The purpose of this study is to assess the humoral immune responses to three different dose schedules of Takeda's Tetravalent Dengue Vaccine Candidate (TDV) administered subcutaneously in healthy participants between 2 and \<18 years of age living in dengue endemic countries.

Timeline

Start
2014-12-05
Primary completion
2019-02-18
Completion
2019-02-18

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Takeda's Tetravalent Dengue Vaccine Candidate (TDV) Vaccine 0.5 ml Subcutaneous

Indications