Ciprofloxacin BioThrax Co-Administration Study
Trial details
- Registry ID
- NCT01753115
- Phase
- Phase 2
Open a linked trial to see its study details and recorded changes, or check the regulatory events below and follow their sources.
Drug identity checked against registry records
Also recorded as AVA; Anthrax Vaccine Adsorbed; Anthrax Vaccine Adsorbed (AVA)
| Trial | Sponsor | Phase | Status | Primary completion |
|---|---|---|---|---|
| Ciprofloxacin BioThrax Co-Administration StudyNCT01753115 | Emergent BioSolutions | Phase 2 | Completed | 2013-08Actual |
| Immunogenicity and Safety Study of a Three-Dose BioThrax® Regimen for Post-Exposure Prophylaxis in Healthy AdultsNCT01491607 | Emergent BioSolutions | Phase 3 | Completed | 2012-05Actual |
| VELOCITY: An Anthrax Vaccine Clinical StudyNCT03877926 | Emergent BioSolutions | Phase 3 | Completed | 2020-08-06Actual |
| A Phase 2 Safety and Immunogenicity Study for an Anthrax Vaccine Using 3 Schedules and Two Dose LevelsNCT01770743 | Emergent BioSolutions | Phase 2 | Completed | 2014-02Actual |
| No regulatory events match this view.Try another date range or view. Events appear after automated source checks. This does not mean no FDA events have occurred. Dates that a source does not disclose stay undisclosed. |