drugset / Trial / NCT02239172
PA83-FhCMB Plant-Derived Recombinant Protective Antigen (rPA) Anthrax Vaccine
Non-randomizedSingle-groupSingle-blindPrevention
Summary
The purposes of this study is to evaluate and compare the safety, reactogenicity, and tolerability of the PA83-FhCMB vaccine candidate delivered at 4 dose levels with Alhydrogel
Timeline
- Start
- 2014-08
- Primary completion
- 2015-05
- Completion
- 2015-05
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | PA83-FhCMB | Vaccine | 12.5 ug | Intramuscular |
| Subject | PA83-FhCMB | Vaccine | 25 ug | Intramuscular |
| Subject | PA83-FhCMB | Vaccine | 50 ug | Intramuscular |
| Subject | PA83-FhCMB | Vaccine | 100 ug | Intramuscular |