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NCT01753115 · ClinicalTrials.gov registry record · Phase 2
Ciprofloxacin BioThrax Co-Administration Study
A Phase 2 study, sponsored by Emergent BioSolutions.
- Completed
- Registry status
- Phase 2
- Development phase
- 154
- Enrollment target
NCT01753115: Completed Phase 2 study, sponsored by Emergent BioSolutions.
NCT01753115 is a Phase 2 study that has completed, run by Emergent BioSolutions. The registered enrollment target is 154 participants, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (16% higher). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01753115, a Phase 2 study, has completed, sponsored by Emergent BioSolutions.
- COMPLETED
- Registry status
- Phase 2
- Development phase
- 154 participants
- Enrollment target
Study Summary
The purpose of this clinical trial is to determine whether there is any effect on the antibiotic, ciprofloxacin when taken before and after administration of a 3-dose series of BioThrax® (Anthrax Vaccine Adsorbed or AVA). This study will be conducted in the United States (US) in 154 healthy male and female volunteer subjects ages 18 to 45. The duration of study participation for each subject will be approximately 76 days (approximately 2.5 months)
Primary Outcome
Ratios of Area Under the Curve from zero to 12 hours (AUC0-12h) and maximum concentration (Cmax) achieved for ciprofloxacin (Day 5/Day 44).
Interventions
- DRUG Ciprofloxacin
- BIOLOGICAL BioThrax
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 154 participants |
| Start Date | 2012-12 |
| Est. Completion | 2013-08 |
| Phase | Phase 2 |
What the finished NCT01753115 record still lists
NCT01753115 is an interventional study that assigns participants to a tested intervention. The registered 154 participants enrollment target is mid-sized for trials with a published cap, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (16% higher).
The record links to 0 conditions, and to 2 interventions - of which Ciprofloxacin is the first listed.
NCT01753115 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01753115 about?
NCT01753115 is a clinical study titled "Ciprofloxacin BioThrax Co-Administration Study". The purpose of this clinical trial is to determine whether there is any effect on the antibiotic, ciprofloxacin when taken before and after administration of a 3-dose series of BioThrax® (Anthrax Vaccine Adsorbed or AVA). This study will be conducted in the United States (US) in 154 healthy male an...
What is the current status of trial NCT01753115?
This trial is currently completed. It is a Phase 2 study. The enrollment target is 154 participants. The study started on 2012-12. Estimated completion is 2013-08.
What interventions are being tested in trial NCT01753115?
The interventions under investigation include: Ciprofloxacin (DRUG), BioThrax (BIOLOGICAL).
Who is sponsoring clinical trial NCT01753115?
This trial is sponsored by Emergent BioSolutions, which has 34 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT01753115's enrollment target sits among peer trials
154 448th of 2000 higher than 1,552 of 2,000 other Phase 2 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 2 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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