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NCT01952444 · ClinicalTrials.gov registry record · Phase 1
Safety, Tolerability and PK of Intravenous (IV) ETI-204 Alone and in Presence of Ciprofloxacin in Adult Volunteers
A Phase 1 study, sponsored by Elusys Therapeutics.
- Completed
- Registry status
- Phase 1
- Development phase
- 40
- Enrollment target
NCT01952444: Completed Phase 1 study, sponsored by Elusys Therapeutics.
NCT01952444 is a Phase 1 study that has completed, run by Elusys Therapeutics. The registered enrollment target is 40 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (33% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01952444, a Phase 1 study, has completed, sponsored by Elusys Therapeutics.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 40 participants
- Enrollment target
Study Summary
Evaluate the safety, tolerability and pharmacokinetics (PK) of intravenous (IV) ETI-204 alone and in the presence of IV and oral ciprofloxacin
Primary Outcome
Safety was assessed for all subjects in the Safety Population by collecting and monitoring vital signs, clinical laboratory tests, ECGs, physical assessments, skin assessments, infusion site assessments, and adverse events (AEs).
Interventions
- DRUG Ciprofloxacin
- BIOLOGICAL ETI-204
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 40 participants |
| Start Date | 2013-10-29 |
| Est. Completion | 2014-04-09 |
| Phase | Phase 1 |
What the finished NCT01952444 record still lists
NCT01952444 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 40 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (33% lower).
The record links to 0 conditions, and to 2 interventions - of which Ciprofloxacin is the first listed.
NCT01952444 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01952444 about?
NCT01952444 is a clinical study titled "Safety, Tolerability and PK of Intravenous (IV) ETI-204 Alone and in Presence of Ciprofloxacin in Adult Volunteers". Evaluate the safety, tolerability and pharmacokinetics (PK) of intravenous (IV) ETI-204 alone and in the presence of IV and oral ciprofloxacin
What is the current status of trial NCT01952444?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 40 participants. The study started on 2013-10-29. Estimated completion is 2014-04-09.
What interventions are being tested in trial NCT01952444?
The interventions under investigation include: Ciprofloxacin (DRUG), ETI-204 (BIOLOGICAL).
Who is sponsoring clinical trial NCT01952444?
This trial is sponsored by Elusys Therapeutics, which has 6 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT01952444's enrollment target sits among peer trials
40 1130th of 2000 higher than 810 of 2,000 other Phase 1 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 1 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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