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NCT02013141 · ClinicalTrials.gov registry record · Phase 1
Telavancin Pediatric PK Study (Ages >12 Months to 17 Years)
A Phase 1 study, sponsored by Cumberland Pharmaceuticals.
- Terminated
- Registry status
- Phase 1
- Development phase
- 22
- Enrollment target
NCT02013141: Clinical Trial Phase 1 study, sponsored by Cumberland Pharmaceuticals.
NCT02013141 is a Phase 1 study that was terminated before completion, run by Cumberland Pharmaceuticals. The registered enrollment target is 22 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (63% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT02013141, a Phase 1 study, was terminated before completion, sponsored by Cumberland Pharmaceuticals.
- TERMINATED
- Registry status
- Phase 1
- Development phase
- 22 participants
- Enrollment target
Study Summary
This is a multicenter, open-label, single-dose pharmacokinetic (PK) study. Infants, children, and adolescents will receive a single 10 mg/kg dose of telavancin infused intravenously (IV) over 60 minutes
Primary Outcome
Plasma telavancin concentrations were measured at 1.0, 1.5, 2.0, 6.0, 12.0, 24.0 hours following IV infusion of telavancin, and area under the curve extrapolated to infinity was calculated for the plasma concentration versus time curves for telavancin following a single 10 mg/kg IV dose.
Interventions
- DRUG Telavancin
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 22 participants |
| Start Date | 2014-12 |
| Est. Completion | 2021-03 |
| Phase | Phase 1 |
Why NCT02013141 stopped before completion
NCT02013141 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 22 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (63% lower).
The record links to 0 conditions, and to 1 intervention - of which Telavancin is the first listed.
NCT02013141 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT02013141 about?
NCT02013141 is a clinical study titled "Telavancin Pediatric PK Study (Ages >12 Months to 17 Years)". This is a multicenter, open-label, single-dose pharmacokinetic (PK) study. Infants, children, and adolescents will receive a single 10 mg/kg dose of telavancin infused intravenously (IV) over 60 minutes
What is the current status of trial NCT02013141?
This trial is currently terminated. It is a Phase 1 study. The enrollment target is 22 participants. The study started on 2014-12. Estimated completion is 2021-03.
What interventions are being tested in trial NCT02013141?
The interventions under investigation include: Telavancin (DRUG).
Who is sponsoring clinical trial NCT02013141?
This trial is sponsored by Cumberland Pharmaceuticals, which has 43 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT02013141's enrollment target sits among peer trials
22 1601st of 2000 higher than 386 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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