drugset / Trial / NCT01193907

Safety and Immunogenicity of Three Formulations of Vi-CRM197 Vaccine Against S. Typhi in Adults (18-40 Years Old)

NCT01193907

Phase 2 Completed 88 enrolled Novartis
RandomizedParallel-groupSingle-blindPrevention

Summary

This trial is aimed to evaluate the safety and immunogenicity profiles of three formulations of Vi-CRM197 conjugate vaccine against S. Typhi in healthy human adults in comparison with the currently licensed Vi polysaccharide vaccine

Timeline

Start
2010-10
Primary completion
2010-11
Completion
2010-11

Drugs

EvaluationDrugModalityDoseRoute
Comparator Vi Polysaccharide Vaccine Vaccine 25 ug
Subject Vi-CRM197 Vaccine 1.25 ug
Subject Vi-CRM197 Vaccine 5 ug
Subject Vi-CRM197 Vaccine 12.5 ug

Indications