drugset / Trial / NCT04862416

Safety and Efficacy of R0.6C Vaccine

NCT04862416 ↗

RandomizedSequentialOpen-labelPrevention

Summary

This is a first-in-human phase I, open-label, single-site, dose escalation study to determine the safety, tolerability and Plasmodium falciparum transmission reducing activity of the R0.6C vaccine in two different adjuvant combinations.

Timeline

Start
2021-05-17
Primary completion
2022-06-29
Completion
2022-06-29

Drugs

EvaluationDrugModalityDoseRoute
Subject R0.6C Vaccine 30 ug Intramuscular
Subject R0.6C Vaccine 100 ug Intramuscular