drugset / Trial / NCT01193907
Safety and Immunogenicity of Three Formulations of Vi-CRM197 Vaccine Against S. Typhi in Adults (18-40 Years Old)
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| 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 | — |