drugset / Trial / NCT02647489

Safety and Immunogenicity of the Placental Malaria Vaccine Candidate PAMVAC Variously Adjuvanted

NCT02647489

RandomizedFactorialQuadruple-blindPrevention

Summary

Despite having developed robust acquired immunity against complications of malaria, women can return to a susceptible state during their first pregnancies and contribute significantly to the burden of severe malaria in highly endemic areas. Naturally acquired protection against placental malaria correlates with the presence of high concentration of immunoglobulin G molecules (IgGs) against VAR2CSA, a parasite protein of the var gene family that is essential for the binding of infected erythrocytes to CSA in the placenta. To induce high concentrations of specific IgGs, subjects will receive escalating doses of PAMVAC vaccine antigen adjuvanted with Alhydrogel, Glucopyranosyl Lipid Adjuvant-Stable Emulsion (GLA-SE) or Glucopyranosyl Lipid Adjuvant-Liposome-QS-21 Formulation (GLA-LSQ). Three injections with the same dosage and adjuvant will be done, each 28 days apart (Day 0, 28 and 56). Control subjects will receive physiological saline instead of the vaccine and dose escalation will be staggered to ensure safety during the trial.

Timeline

Start
2016-05
Primary completion
2017-11-10
Completion
2017-11-10

Drugs

EvaluationDrugModalityDoseRoute
Subject PAMVAC Protein / enzyme biologic 20 ug Intramuscular
Subject PAMVAC Protein / enzyme biologic 50 ug Intramuscular
Subject PAMVAC Protein / enzyme biologic 100 ug Intramuscular
Background Aluminum hydroxide Unknown Intramuscular
Background GLA-LSQ Other / unclassified Intramuscular
Background GLA-SE Other / unclassified Intramuscular

Indications