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A Study to Evaluate Single Agent Selinexor Versus Physician's Choice in Participants With Previously Treated Myelofibrosis
NCT04562870 · View on ClinicalTrials.gov ↗
Study Summary
This is a Phase 2, multicenter, two-arm, open-label study to evaluate the safety and efficacy of selinexor versus treatment per physician's choice (PC) in participants with myelofibrosis (MF) who had at least 6 months of treatment with a Janus kinase (JAK)1/2 inhibitor. Study participants will be randomized in a 1:1 ratio to either receive selinexor or physicians' choice of treatment.
Conditions Studied
Interventions
- DRUG Selinexor
- OTHER Physician's Choice Treatment
Study Locations (20)
Other
- Centre Hospitalier Universitaire d'Angers (CHU Angers) — Angers
- Università degli Studi di Firenze - Azienda Ospedaliero - Universitaria Careggi - Dipartimento di medicina sperimentale e clinica — Florence
- Azienda Unita Sanitaria Locale Latina - Ospedale Santa Maria Goretti — Latina
- University of Perugia Department of Medicine Hematology Section — Perugia
- Asst Settelaghi, Ospedale Di Circolo E Fondazione Macchi — Varese
- Pratia Onkologia Katowice — Katowice
Jiangsu
- Affiliated Hospital of Nantong University — Nantong
- The Second Affiliated Hospital of Soochow University — Suzhou
- Suzhou University -The First Affiliated Hospital — Suzhou
California
- The Oncology Institute of Hope and Innovation — Pasadena
Colorado
- Rocky Mountain Cancer Centers, LLP — Aurora
Illinois
- Illinois Cancer Specialist — Niles
Texas
- Texas Oncology - Northeast Texas — Tyler
Beijing Municipality
- Peking Union Medical College Hospital — Beijing
Hubei
- Union Hospital, Tongji Medical College, Huazhong University of Science and Technology — Wuhan
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 112 participants |
| Start Date | 2021-03-17 |
| Est. Completion | 2026-09 |
| Phase | Phase 2 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT04562870
The ClinicalTrials.gov registry entry for NCT04562870 describes a study currently listed as active not recruiting. It is categorized as Phase 2, 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 112 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Karyopharm Therapeutics, which has 36 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 1 condition, with Myelofibrosis appearing as the primary indexed condition, and to 2 interventions — of which Selinexor 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: NCT04562870 reports 20 study locations spanning 13 distinct geographic areas — top geographies include Other, Jiangsu, California. 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 NCT04562870 about?
NCT04562870 is a clinical study titled "A Study to Evaluate Single Agent Selinexor Versus Physician's Choice in Participants With Previously Treated Myelofibrosis". This is a Phase 2, multicenter, two-arm, open-label study to evaluate the safety and efficacy of selinexor versus treatment per physician's choice (PC) in participants with myelofibrosis (MF) who had at least 6 months of treatment with a Janus kinase (JAK)1/2 inhibitor. Study participants will be ra...
What is the current status of trial NCT04562870?
This trial is currently active not recruiting. It is a Phase 2 study. The enrollment target is 112 participants. The study started on 2021-03-17. Estimated completion is 2026-09.
What conditions does trial NCT04562870 study?
This clinical trial studies the following conditions: Myelofibrosis. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT04562870?
The interventions under investigation include: Selinexor (DRUG), Physician's Choice Treatment (OTHER). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT04562870?
This trial is sponsored by Karyopharm Therapeutics, which has 36 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT04562870 being conducted?
This trial has 20 study locations across California, Colorado, Illinois, Texas, Beijing Municipality. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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