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NCT02245243 · ClinicalTrials.gov registry record · Phase 1
Pharmacokinetics of Delafloxacin in Subjects With and Without Hepatic Impairment
A Phase 1 study, sponsored by Melinta Therapeutics.
- Completed
- Registry status
- Phase 1
- Development phase
- 40
- Enrollment target
NCT02245243: Completed Phase 1 study, sponsored by Melinta Therapeutics.
NCT02245243 is a Phase 1 study that has completed, run by Melinta 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
NCT02245243, a Phase 1 study, has completed, sponsored by Melinta Therapeutics.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 40 participants
- Enrollment target
Study Summary
The purpose of this study is to evaluate the pharmacokinetic profile, safety, and tolerability of a single intravenous (IV) dose of delafloxacin in normal healthy subjects and subjects with mild, moderate, or severe hepatic impairment.
Interventions
- DRUG Delafloxacin
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 40 participants |
| Start Date | 2014-09 |
| Est. Completion | 2015-02 |
| Phase | Phase 1 |
What the finished NCT02245243 record still lists
NCT02245243 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 1 intervention - of which Delafloxacin is the first listed.
NCT02245243 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT02245243 about?
NCT02245243 is a clinical study titled "Pharmacokinetics of Delafloxacin in Subjects With and Without Hepatic Impairment". The purpose of this study is to evaluate the pharmacokinetic profile, safety, and tolerability of a single intravenous (IV) dose of delafloxacin in normal healthy subjects and subjects with mild, moderate, or severe hepatic impairment.
What is the current status of trial NCT02245243?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 40 participants. The study started on 2014-09. Estimated completion is 2015-02.
What interventions are being tested in trial NCT02245243?
The interventions under investigation include: Delafloxacin (DRUG).
Who is sponsoring clinical trial NCT02245243?
This trial is sponsored by Melinta Therapeutics, which has 31 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT02245243'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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