drugset / Trial / NCT01317667
Safety and Immunogenicity Study of Recombinant Ricin Toxin A-Chain Vaccine (RVEc™)
Phase 1
Completed
30 enrolled
U.S. Army Medical Research and Development Command
US Army Medical Research Institute of Infectious Diseases · collab
RandomizedParallel-groupOpen-labelOther
Summary
This study is a Phase 1, escalating, multiple-dose, single-center study to evaluate the safety and immunogenicity of the RVEc vaccine. The two principal hypotheses to be tested are: RVEc vaccine will display an acceptable safety profile as determined by adverse event data and RVEc vaccine will elicit ELISA immunoglobulin G (IgG) titers greater than or equal to 1:500 and toxin-neutralizing antibody (TNA) anti-ricin toxin-neutralizing antibody titers greater than or equal to 1:50 in vaccine recipients.
Timeline
- Start
- 2011-03
- Primary completion
- 2012-11
- Completion
- 2014-12
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | RVEc | Vaccine | 20 ug | — |
| Subject | RVEc | Vaccine | 50 ug | — |
| Subject | RVEc | Vaccine | 100 ug | — |