drugset / Trial / NCT00842530

Efficacy and Safety of Dengue Vaccine in Healthy Children

NCT00842530

Phase 2 Completed 4002 enrolled Sanofi Pasteur, a Sanofi Company
RandomizedParallel-groupDouble-blindPrevention

Summary

The primary objective of the study was to assess the efficacy of CYD dengue vaccine after three injections in preventing symptomatic virologically-confirmed dengue (VCD) cases, regardless of the severity, due to any of the four serotypes in children aged 4 to 11 years at the time of inclusion. Secondary objectives included to assess: * Vaccine efficacy against severe VCD cases * Vaccine efficacy against VCD cases following at least two injections with CYD dengue vaccine * Immune response to CYD dengue vaccine * Safety profile of CYD dengue vaccine. Safety assessments include solicited reactions within 7 or 14 days after each injection, unsolicited adverse events within 28 days after each injection, and serious adverse events during the study period. Other objectives included: * Vaccine efficacy against VCD cases following at least one injection with CYD dengue vaccine * Vaccine efficacy against VCD cases due to each serotype * Participants with clinical signs and symptoms for VCD

Timeline

Start
2009-02
Primary completion
2013-09
Completion
2014-02

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject CYD Dengue Vaccine Vaccine 0.5 ml Subcutaneous
Comparator Rabies vaccine Vaccine 0.5 ml Subcutaneous