drugset / Trial / NCT02339155
Effect of Raxibacumab on Immunogenicity of Anthrax Vaccine Adsorbed
RandomizedParallel-groupOpen-labelTreatment
Summary
This study, as a post-marketing commitment to the Food and Drug Administration, is designed to detect the effect of raxibacumab on anthrax vaccine adsorbed (AVA) immunogenicity in a healthy volunteer population. This is a randomized, open-label, parallel group, two arm study to compare the immunogenicity of AVA at 4 weeks after the first AVA dose, when AVA is administered alone or concomitantly with raxibacumab. The study is planned to enroll approximately 30 to 534 subjects in up to 3 cohorts. The total duration of the study will be approximately 26 weeks. The dates reflect cohort 1.
Timeline
- Start
- 2015-02-24
- Primary completion
- 2017-01-03
- Completion
- 2017-06-06
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | BioThrax | Vaccine | 0.5 ml | Subcutaneous |
| Subject | Raxibacumab | Monoclonal antibody | 40 mg/kg | Intravenous |
| Background | Diphenhydramine | Unknown | 25 mg | Oral |
| Background | Diphenhydramine | Unknown | 50 mg | Oral |