drugset / Trial / NCT05135273

Study of the Transmission-Blocking Vaccine Pfs230D1-EPA/Matrix-M Against Malaria in Adults in Mali

NCT05135273

RandomizedParallel-groupDouble-blindPrevention

Summary

Background: Researchers are trying to develop a vaccine that will safely reduce the spread of malaria in the community by preventing mosquitos from carrying malaria from person to person. Objective: To assess in African adults the safety of and immune response to the administration of Pfs230D1-EPA/Matrix-M vaccine as compared to the rabies vaccine control. Eligibility: Healthy adults (18 to 50 years of age) who reside in Sotuba and surrounding villages in Mali Design: Participants will be screened with: * Medical history * Physical exam * Blood, urine, and heart tests * Malaria comprehension exam Participants will be randomly assigned to get either the experimental vaccine or the approved rabies vaccine. They will not know which they are getting. Participants will get 3 doses of the study or comparator vaccine via injection in the upper arm. This occurs at the first visit, 1 month, and 2 months later. Participants will have up to 23 scheduled visits over 14 to 16 months. Each visit includes a physical exam, and blood will be collected at most visits. Participants will be followed up to 1 year after the final vaccination. If participants develop an injection site rash or reaction, photographs may be taken of the site.

Timeline

Start
2021-10-22
Primary completion
2023-02-17
Completion
2023-06-21

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Matrix-M1 Adjuvant Other / unclassified 25 ug Intramuscular
Subject Matrix-M1 Adjuvant Other / unclassified 50 ug Intramuscular
Subject Pfs230D1-EPA Vaccine 12.5 ug Intramuscular
Subject Pfs230D1-EPA Vaccine 20 ug Intramuscular
Subject Pfs230D1-EPA Vaccine 40 ug Intramuscular
Comparator Rabies vaccine Vaccine Intramuscular