drugset / Trial / NCT00875524

Study of ChimeriVax™ Tetravalent Dengue Vaccine in Healthy Subjects

NCT00875524

Phase 2 Completed 180 enrolled Sanofi Pasteur, a Sanofi Company
RandomizedParallel-groupTriple-blindPrevention

Summary

This trial evaluated the use of a tetravalent vaccine against dengue. Primary objectives: * To describe the humoral immune response to dengue before and after each vaccination with tetravalent dengue vaccine in adults, adolescents, and children. * To evaluate the safety of each vaccination with tetravalent dengue vaccine in the 4 age cohorts. * To evaluate the persistence of antibodies against dengue during 5 years after the first vaccination with tetravalent dengue vaccine in the 4 age cohorts.

Timeline

Start
2009-03
Primary completion
2014-08
Completion
2014-12

Drugs

EvaluationDrugModalityDoseRoute
Subject CYD Dengue Vaccine Vaccine 0.5 ml Subcutaneous
Comparator Meningococcal Polysaccharide A+C Vaccine 0.5 ml Subcutaneous
Comparator Typhim Vi Vaccine 0.5 ml Subcutaneous