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NCT01340651 · ClinicalTrials.gov registry record · Phase 2
Study of Ruxolitinib (INCB018424) Sustained Release Formulation in Myelofibrosis Patients
A Phase 2 study of Myelofibrosis, sponsored by Incyte Corporation.
- Completed
- Registry status
- Phase 2
- Development phase
- 41
- Enrollment target
- 3
- Study locations
NCT01340651 is a Phase 2 study of Myelofibrosis that has completed, run by Incyte Corporation. The registered enrollment target is 41 participants, below the 195-participant average among 61 other Myelofibrosis trials with a reported enrollment target (79% lower). The trial reports 3 study locations across 3 states.
The verdict
NCT01340651, a Phase 2 study of Myelofibrosis, has completed, sponsored by Incyte Corporation.
- COMPLETED
- Registry status
- Phase 2
- Development phase
- 41 participants
- Enrollment target
- 3
- Study locations
Study Summary
The purpose of this study is to determine the safety and tolerability of ruxolitinib (INCB018424) sustained release (SR) formulation in participants with primary myelofibrosis (PMF), post-polycythemia vera MF (PPV-MF), and post-essential thrombocythemia MF (PET-MF).
Conditions Studied
Interventions
- DRUG Ruxolitinib
Study Locations (3)
Arizona
- - Scottsdale
Florida
- - Winter Park
Texas
- - Houston
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 41 participants |
| Start Date | 2011-03 |
| Est. Completion | 2012-07 |
| Phase | Phase 2 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01340651
The ClinicalTrials.gov registry entry for NCT01340651 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 41 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 195-participant average among 61 other Myelofibrosis trials with a reported enrollment target (79% lower). The listed sponsor is Incyte Corporation, which has 239 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Myelofibrosis appearing as the primary indexed condition, and to 1 intervention - of which Ruxolitinib is the first listed.
NCT01340651 reports 3 study locations spanning 3 distinct geographic areas - top geographies include Arizona, Florida, Texas.
Frequently Asked Questions
What is clinical trial NCT01340651 about?
NCT01340651 is a clinical study titled "Study of Ruxolitinib (INCB018424) Sustained Release Formulation in Myelofibrosis Patients". The purpose of this study is to determine the safety and tolerability of ruxolitinib (INCB018424) sustained release (SR) formulation in participants with primary myelofibrosis (PMF), post-polycythemia vera MF (PPV-MF), and post-essential thrombocythemia MF (PET-MF).
What is the current status of trial NCT01340651?
This trial is currently completed. It is a Phase 2 study. The enrollment target is 41 participants. The study started on 2011-03. Estimated completion is 2012-07.
What conditions does trial NCT01340651 study?
This clinical trial studies the following conditions: Myelofibrosis.
What interventions are being tested in trial NCT01340651?
The interventions under investigation include: Ruxolitinib (DRUG).
Who is sponsoring clinical trial NCT01340651?
This trial is sponsored by Incyte Corporation, which has 239 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT01340651 being conducted?
This trial has 3 study locations across Arizona, Florida, Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Read our methodology - how this data is sourced, computed, and verified.
Related
Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.