drugset / Trial / NCT02925403

A Study to Assess the Safety and Immunogenicity of the Malaria Vaccine, R21, With Matrix-M1 Adjuvant

NCT02925403

Phase 1/2 Completed 13 enrolled University of Oxford
RandomizedParallel-groupSingle-blindPrevention

Summary

This is a study in which healthy adult volunteers will be given either an experimental Malaria vaccine or a saline control vaccine. Each volunteer will receive three vaccinations in total. Volunteers will be randomly allocated to one of two groups: Group 1 will receive a low dose of the Malaria vaccine on days 0, 28, and 56. Group 2 will receive a saline solution on days 0, 28, and 56.

Timeline

Start
2016-08-26
Primary completion
2017-02-15
Completion
2017-02-15

Publications

Drugs

EvaluationDrugModalityDoseRoute
Comparator R21 Vaccine 10 ug
Comparator R21 Vaccine 50 ug
Comparator Matrix-M1 Other / unclassified 50 ug

Indications