drugset / Trial / NCT02658253

Trial to Evaluate the Safety and Immunogenicity of a Placental Malaria Vaccine Candidate (PRIMVAC ) in Healthy Adults

NCT02658253

RandomizedParallel-groupDouble-blindPrevention

Summary

The primary objective of the study is to evaluate the safety of 3 different dosages (20µg - 50µg and 100µg) of a placental malaria vaccine candidate (PRIMVAC vaccine) adjuvanted either with Alhydrogel® or GLA-SE, and administered at D0, D28 and D56 in healthy European and Burkinabe adults. The safety and the tolerability of the vaccine will be assessed on the rate of solicited and unsolicited events/reactions The safety profile will included local and systemic reactions/events as well as the biological safety, based on a clinically significant change of the baseline value of the main biological criteria

Timeline

Start
2016-01
Primary completion
2018-09-19
Completion
2019-02-21

Drugs

EvaluationDrugModalityDoseRoute
Subject Aluminum hydroxide Unknown 0.85 mg Intramuscular
Subject GLA-SE Other / unclassified 2.5 ug Intramuscular
Subject GLA-SE Other / unclassified 2.56 ug Intramuscular
Subject PRIMVAC Unknown 20 ug Intramuscular
Subject PRIMVAC Unknown 50 ug Intramuscular
Subject PRIMVAC Unknown 100 ug Intramuscular

Indications