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NCT02823171 · ClinicalTrials.gov registry record · Phase 1
To Assess the Bioequivalence of Two Pacritinib Drug Product Formulations and FMI Formulation Following Oral Administration in Healthy Subjects
A Phase 1 study of Healthy, sponsored by CTI BioPharma.
- Completed
- Registry status
- Phase 1
- Development phase
- 28
- Enrollment target
- 1
- Study location
NCT02823171: Completed Phase 1 study of Healthy, sponsored by CTI BioPharma.
NCT02823171 is a Phase 1 study of Healthy that has completed, run by CTI BioPharma. The registered enrollment target is 28 participants, below the 647-participant average among 1,090 other Healthy trials with a reported enrollment target (96% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT02823171, a Phase 1 study of Healthy, has completed, sponsored by CTI BioPharma.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 28 participants
- Enrollment target
- 1
- Study location
Study Summary
A Phase 1, Open-Label, Single-Dose, Randomized, 2-Period Crossover Study to Assess the Bioequivalence of Two Pacritinib Drug Product Formulations (Phase 3 Clinical Trial \[P3CT\] Formulation \[Reference\] and Final Market Image \[FMI\] Formulation \[Test\]) Following Oral Administration in Healthy Subjects
Conditions Studied
Interventions
- DRUG Treatment A: 400 mg Pacritinib P3CT
- DRUG Treatment B: 400 mg of pacritinib FMI
Study Locations (1)
Indiana
- Covance Clinical Research Unit Inc. - Evansville
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 28 participants |
| Start Date | 2015-08 |
| Est. Completion | 2015-09 |
| Phase | Phase 1 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02823171
The ClinicalTrials.gov registry entry for NCT02823171 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 28 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 647-participant average among 1,090 other Healthy trials with a reported enrollment target (96% lower). The listed sponsor is CTI BioPharma, which has 28 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Healthy appearing as the primary indexed condition, and to 2 interventions - of which Treatment A: 400 mg Pacritinib P3CT is the first listed.
NCT02823171 reports 1 study location spanning 1 distinct geographic area - top geographies include Indiana.
Frequently Asked Questions
What is clinical trial NCT02823171 about?
NCT02823171 is a clinical study titled "To Assess the Bioequivalence of Two Pacritinib Drug Product Formulations and FMI Formulation Following Oral Administration in Healthy Subjects". A Phase 1, Open-Label, Single-Dose, Randomized, 2-Period Crossover Study to Assess the Bioequivalence of Two Pacritinib Drug Product Formulations (Phase 3 Clinical Trial \[P3CT\] Formulation \[Reference\] and Final Market Image \[FMI\] Formulation \[Test\]) Following Oral Administration in Healthy S...
What is the current status of trial NCT02823171?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 28 participants. The study started on 2015-08. Estimated completion is 2015-09.
What conditions does trial NCT02823171 study?
This clinical trial studies the following conditions: Healthy.
What interventions are being tested in trial NCT02823171?
The interventions under investigation include: Treatment A: 400 mg Pacritinib P3CT (DRUG), Treatment B: 400 mg of pacritinib FMI (DRUG).
Who is sponsoring clinical trial NCT02823171?
This trial is sponsored by CTI BioPharma, which has 28 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT02823171 being conducted?
This trial has 1 study location across Indiana. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Related
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