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Safety and Tolerability Study of INCB057643 in Participants With Myelofibrosis and Other Advanced Myeloid Neoplasms
NCT04279847 · View on ClinicalTrials.gov ↗
Study Summary
The purpose of this study is to evaluate the safety, tolerability, and preliminary efficacy of INCB057643 as monotherapy or combination with ruxolitinib for participants with myelofibrosis (MF) and other myeloid neoplasms.
Conditions Studied
Interventions
- DRUG Ruxolitinib
- DRUG INCB057643
Study Locations (20)
New York
- Nyu Langone Health - Long Island Hospital — Mineola
- Nyu Langone Laura and Isaac Perlmutter Cancer Center — New York
- Weill Medical College of Cornell University — New York
Texas
- Texas Oncology-Baylor Sammons Cancer Center — Dallas
- Md Anderson Cancer Center — Houston
- Oncology Consultants — Houston
Ohio
- University of Cincinnati Cancer Institute — Cincinnati
- Ohio State University — Columbus
Alabama
- University of Alabama At Birmingham — Birmingham
Colorado
- University of Colorado Cancer Center — Aurora
Florida
- University of Miami Sylvester Comprehensive Cancer Center — Miami
Georgia
- Emory University-Winship Cancer Institute — Atlanta
Iowa
- University of Iowa Hospital and Clinics — Iowa City
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 140 participants |
| Start Date | 2021-02-23 |
| Est. Completion | 2027-04-30 |
| Phase | Phase 1 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT04279847
The ClinicalTrials.gov registry entry for NCT04279847 describes a study currently listed as active not recruiting. It is categorized as Phase 1, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 140 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Incyte Corporation, which has 163 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 7 conditions, with Myelodysplastic Syndrome appearing as the primary indexed condition, and to 2 interventions — of which Ruxolitinib is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT04279847 reports 20 study locations spanning 15 distinct geographic areas — top geographies include New York, Texas, Ohio. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT04279847 about?
NCT04279847 is a clinical study titled "Safety and Tolerability Study of INCB057643 in Participants With Myelofibrosis and Other Advanced Myeloid Neoplasms". The purpose of this study is to evaluate the safety, tolerability, and preliminary efficacy of INCB057643 as monotherapy or combination with ruxolitinib for participants with myelofibrosis (MF) and other myeloid neoplasms.
What is the current status of trial NCT04279847?
This trial is currently active not recruiting. It is a Phase 1 study. The enrollment target is 140 participants. The study started on 2021-02-23. Estimated completion is 2027-04-30.
What conditions does trial NCT04279847 study?
This clinical trial studies the following conditions: Myelodysplastic Syndrome, Myelofibrosis, Myeloproliferative Neoplasm, ET (Essential Thrombocythemia), Myelodysplastic/Myeloproliferative Neoplasm Overlap Syndrome. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT04279847?
The interventions under investigation include: Ruxolitinib (DRUG), INCB057643 (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT04279847?
This trial is sponsored by Incyte Corporation, which has 163 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT04279847 being conducted?
This trial has 20 study locations across Alabama, Colorado, Florida, Georgia, Iowa. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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