drugset / Trial / NCT01254422

Study of a Tetravalent Dengue Vaccine in Healthy Children Aged 2 to 11 Years in Malaysia

NCT01254422

Phase 3 Completed 250 enrolled Sanofi
RandomizedParallel-groupTriple-blindPrevention

Summary

The purpose of this study was to evaluate the safety and immunogenicity of Phase III lots of the CYD dengue vaccine in a pediatric population in Malaysia. Primary Objectives: * To describe the safety (in terms of solicited and unsolicited adverse events) of the CYD dengue vaccine in all participants after each injection. * To describe the antibody response to each dengue virus serotype post-injection 2 and post-injection 3.

Timeline

Start
2010-12-02
Primary completion
2012-09-28
Completion
2013-01

Drugs

EvaluationDrugModalityDoseRoute
Subject CYD-TDV Vaccine 0.5 ml Subcutaneous