drugset / Trial / NCT02676895

A Study of the Safety and Immune Response of 2 Doses of a New Shigella Vaccine in Kenyan Adults

NCT02676895

Phase 2 Completed 74 enrolled GlaxoSmithKline
RandomizedParallel-groupQuadruple-blindPrevention

Summary

The purpose of this study is to evaluate the safety and the immunogenicity of two different doses of the GVGH S. sonnei vaccine in healthy adults and represents the first step towards testing of the GMMA vaccine in the vaccine target population of children from developing countries where shigellosis is endemic.

Timeline

Start
2016-08-08
Primary completion
2017-03-10
Completion
2017-03-10

Drugs

EvaluationDrugModalityDoseRoute
Subject 1790GAHB Vaccine 25 ug Intramuscular
Subject 1790GAHB Vaccine 100 ug Intramuscular
Comparator Boostrix Vaccine
Comparator Menveo Vaccine

Indications