drugset / Trial / NCT00730288

Study of ChimeriVax™ Dengue Tetravalent Vaccine in Adult Subjects

NCT00730288 ↗

Phase 2 Completed 35 enrolled Sanofi
RandomizedParallel-groupOpen-labelPrevention

Summary

To evaluate effect of previous flavivirus exposure on the safety and immunogenicity of the ChimeriVax™ dengue tetravalent vaccine Primary Objectives: * To describe the safety of one injection of ChimeriVax™ dengue tetravalent vaccine. * To describe the immune response against dengue before and after one injection of ChimeriVax™ dengue tetravalent vaccine

Timeline

Start
2006-08
Primary completion
2007-08
Completion
2008-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Chimeric dengue serotype (1, 2, 3, 4) Vaccine 0.5 ml Subcutaneous