drugset / Trial / NCT01438996
Extension Study of H01_04TP to Evaluate the Booster Response Induced by Vi-CRM197 in Adults
Non-randomizedParallel-groupOpen-labelPrevention
Summary
The purpose of this study is to evaluate the immunogenicity and the kinetics of the anti-Vi antibody response following secondary vaccination with the Novartis Vaccines Institute for Global Health (NVGH) Vi-CRM197 vaccine in healthy adults previously vaccinated with either the NVGH Vi-CRM197 or Vi-polysaccharide (Typherix) in the H01\_04TP study (NCT01193907) and the immunogenicity and the kinetics of the anti-Vi antibody response following primary vaccination with the NVGH Vi-CRM197 vaccine in naïve healthy adults.
Timeline
- Start
- 2011-10
- Primary completion
- 2011-12
- Completion
- 2011-12
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | NVGH Vi-CRM197 | Vaccine | 5 ug | — |