drugset / Trial / NCT02948829

Safety and Immunogenicity of Takeda's Tetravalent Dengue Vaccine (TDV) in Healthy Children

NCT02948829 ↗

Phase 2 Completed 200 enrolled Takeda
NaSingle-groupOpen-labelPrevention

Summary

The purpose of this study is to assess the cellular immune responses following 2 doses given 3 months apart of tetravalent dengue vaccine candidate (TDV) in 4 to 16 years' healthy participants.

Timeline

Start
2017-04-03
Primary completion
2017-10-16
Completion
2020-12-14

Drugs

EvaluationDrugModalityDoseRoute
Subject TDV Vaccine 0.5 ml Subcutaneous

Indications

No indication recorded.