At a glance
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Immunogenicity and Safety of ChimeriVax™ Tetravalent Dengue Vaccine in Healthy Subjects Aged 2 to 45 Years in Viet Nam
In Brief
A Phase 2 clinical trial evaluating CYD dengue vaccine serotypes (1, 2, 3, 4). and Meningococcal Polysaccharide A+C; NaCl; Typhoid Vi polysaccharide for Dengue Virus and 3 related conditions. Completed, enrolled 180 participants across 1 site.
Detailed 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.
Study Details
Timeline
Interventions
0.5 mL, Subcutaneous
Each at 0.5 mL, Subcutaneous, respectively