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NCT02807207 · ClinicalTrials.gov registry record · Phase 1
To Evaluate the Cardiac Safety and PK Following a Single Oral Dose Administration of Pacritinib in Healthy Subjects
A Phase 1 study, sponsored by CTI BioPharma.
- Completed
- Registry status
- Phase 1
- Development phase
- 42
- Enrollment target
NCT02807207: Completed Phase 1 study, sponsored by CTI BioPharma.
NCT02807207 is a Phase 1 study that has completed, run by CTI BioPharma. The registered enrollment target is 42 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (30% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT02807207, a Phase 1 study, has completed, sponsored by CTI BioPharma.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 42 participants
- Enrollment target
Study Summary
The primary objective is to evaluate the cardiac safety of a single oral dose (400 mg) of pacritinib compared to placebo on the QT calculated using the Fridericia correction (QTcF) interval in healthy subjects.
Primary Outcome
To evaluate the cardiac safety of a single oral dose (400 mg) of pacritinib compared to placebo
Interventions
- DRUG A: pacritinib
- OTHER B: Placebo
- DRUG C: moxifloxacin
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 42 participants |
| Start Date | 2014-10 |
| Est. Completion | 2014-12 |
| Phase | Phase 1 |
What the finished NCT02807207 record still lists
NCT02807207 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 42 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (30% lower).
The record links to 0 conditions, and to 3 interventions - of which A: pacritinib is the first listed.
NCT02807207 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT02807207 about?
NCT02807207 is a clinical study titled "To Evaluate the Cardiac Safety and PK Following a Single Oral Dose Administration of Pacritinib in Healthy Subjects". The primary objective is to evaluate the cardiac safety of a single oral dose (400 mg) of pacritinib compared to placebo on the QT calculated using the Fridericia correction (QTcF) interval in healthy subjects.
What is the current status of trial NCT02807207?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 42 participants. The study started on 2014-10. Estimated completion is 2014-12.
What interventions are being tested in trial NCT02807207?
The interventions under investigation include: A: pacritinib (DRUG), B: Placebo (OTHER), C: moxifloxacin (DRUG).
Who is sponsoring clinical trial NCT02807207?
This trial is sponsored by CTI BioPharma, which has 28 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT02807207's enrollment target sits among peer trials
42 1105th of 2000 higher than 876 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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