drugset / Trial / NCT02013687
Safety and Immunogenicity of Plant-Derived Pfs25 VLP-FhCMB Malaria Transmission Blocking Vaccine in Healthy Adults
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| 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 | — |