drugset / Trial / NCT02013687

Safety and Immunogenicity of Plant-Derived Pfs25 VLP-FhCMB Malaria Transmission Blocking Vaccine in Healthy Adults

NCT02013687 ↗

Phase 1 Completed 44 enrolled Fraunhofer, Center for Molecular Biotechnology
Non-randomizedParallel-groupOpen-labelPrevention

Summary

This study is a Phase 1, dose escalation, first-in-human study designed primarily to evaluate the safety of the purified plant-derived Pfs25 VLP combined with Alhydrogel adjuvant

Timeline

Start
2013-10
Primary completion
2014-08
Completion
2015-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Pfs25 VLP-FhCMB Vaccine 2 ug —
Subject Pfs25 VLP-FhCMB Vaccine 10 ug —
Subject Pfs25 VLP-FhCMB Vaccine 30 ug —
Subject Pfs25 VLP-FhCMB Vaccine 100 ug —

Indications