drugset / Trial / NCT03926455

Safety and Immunogenicity of Typhax, a Typhoid Vaccine

NCT03926455

Phase 1 Completed 45 enrolled Matrivax Research and Development Corporation
RandomizedSequentialDouble-blindPrevention

Summary

This was a randomized, double-blind, ascending dose study conducted at a single clinical research center.

Timeline

Start
2016-03-28
Primary completion
2017-02-15
Completion
2017-02-15

Drugs

EvaluationDrugModalityDoseRoute
Subject Typhax Vaccine 0.5 ug Intramuscular
Subject Typhax Vaccine 2.5 ug Intramuscular
Subject Typhax Vaccine 10 ug Intramuscular
Comparator Typhim Vi Vaccine 25 ug Intramuscular

Indications