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NCT02244827 · ClinicalTrials.gov registry record · Phase 1
Pharmacokinetics of WCK 2349 In Patients With Hepatic Impairment
A Phase 1 study, sponsored by Wockhardt.
- Completed
- Registry status
- Phase 1
- Development phase
- 48
- Enrollment target
NCT02244827: Completed Phase 1 study, sponsored by Wockhardt.
NCT02244827 is a Phase 1 study that has completed, run by Wockhardt. The registered enrollment target is 48 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (20% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT02244827, a Phase 1 study, has completed, sponsored by Wockhardt.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 48 participants
- Enrollment target
Study Summary
This study is aimed to compare the pharmacokinetics of levonadifloxacin and its sulfate metabolite after a single dose of oral WCK 2349 1000 mg in patients with hepatic impairment and healthy volunteers.
Primary Outcome
To compare the pharmacokinetics of levonadifloxacin and its sulfate metabolite after a single dose of oral WCK 2349 in patients with hepatic impairment and healthy volunteers
Interventions
- DRUG WCK 2349
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 48 participants |
| Start Date | 2014-09 |
| Est. Completion | 2015-06 |
| Phase | Phase 1 |
What the finished NCT02244827 record still lists
NCT02244827 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 48 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (20% lower).
The record links to 0 conditions, and to 1 intervention - of which WCK 2349 is the first listed.
NCT02244827 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT02244827 about?
NCT02244827 is a clinical study titled "Pharmacokinetics of WCK 2349 In Patients With Hepatic Impairment". This study is aimed to compare the pharmacokinetics of levonadifloxacin and its sulfate metabolite after a single dose of oral WCK 2349 1000 mg in patients with hepatic impairment and healthy volunteers.
What is the current status of trial NCT02244827?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 48 participants. The study started on 2014-09. Estimated completion is 2015-06.
What interventions are being tested in trial NCT02244827?
The interventions under investigation include: WCK 2349 (DRUG).
Who is sponsoring clinical trial NCT02244827?
This trial is sponsored by Wockhardt, which has 27 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT02244827's enrollment target sits among peer trials
48 1025th of 2000 higher than 948 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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