drugset / Trial / NCT03342898

Immunogenicity and Safety of Tetravalent Dengue Vaccine (TDV) Administered With a Yellow Fever Vaccine in Adults

NCT03342898

Phase 3 Completed 900 enrolled Takeda
RandomizedParallel-groupSingle-blindPrevention

Summary

The main purpose of this study is to assess the immunogenicity and safety of the concomitant and sequential administration of yellow fever (YF) vaccine and tetravalent dengue vaccine (TDV) in healthy participants aged 18 to 60 years living in country non-endemic for both dengue and YF.

Timeline

Start
2018-02-28
Primary completion
2018-05-09
Completion
2019-05-22

Drugs

EvaluationDrugModalityDoseRoute
Subject DENVax Unknown 0.5 ml Subcutaneous
Subject YF-17D Vaccine 0.5 ml Subcutaneous

Indications