drugset / Trial / NCT01438996

Extension Study of H01_04TP to Evaluate the Booster Response Induced by Vi-CRM197 in Adults

NCT01438996 ↗

Phase 2 Completed 51 enrolled Novartis
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

EvaluationDrugModalityDoseRoute
Subject NVGH Vi-CRM197 Vaccine 5 ug —

Indications