drugset / Trial / NCT03341637

Immunogenicity and Safety of Tetravalent Dengue Vaccine (TDV) in Adolescents in Non-Endemic Area(s)

NCT03341637

Phase 3 Completed 400 enrolled Takeda
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study was to describe the neutralizing antibody response against each dengue serotype at 1 month post second dose of TDV or placebo in dengue-naive adolescent participants.

Timeline

Start
2017-12-14
Primary completion
2019-01-26
Completion
2019-01-26

Drugs

EvaluationDrugModalityDoseRoute
Subject DENGUE VIRUS, LIVE ATTENUATED Vaccine 0.5 ml Subcutaneous

Indications