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A Study of Selinexor Monotherapy in Subjects With JAK Inhibitor-naïve Myelofibrosis and Moderate Thrombocytopenia
NCT05980806 · View on ClinicalTrials.gov ↗
Study Summary
The main purpose of this study is to evaluate the efficacy of selinexor in JAKi-naïve participants with myelofibrosis (MF) and with normal platelet counts or with mild to moderate thrombocytopenia based on spleen volume reduction (SVR). Additional efficacy and safety parameters will also be assessed during the study.
Conditions Studied
Interventions
- DRUG Ruxolitinib
- DRUG Momelotinib
- DRUG Pacritinib
- DRUG Selinexor 60 mg
- DRUG Selinexor 40 mg
Study Locations (20)
Other
- UZ Gent — Ghent
- UZ Leuven - Campus Gasthuisberg — Leuven
- University Multiprofile Hospital for Active Treatment Sveti George - Base 1 — Plovdiv
- University Hospital Sv.Ivan Rilski - Sofia — Sofia
- University Multiprofile Hospital for Active Treatment Aleksandrovska — Sofia
- Specialized Hospital for Active Treatment of Hematological Diseases - EAD Sofia — Sofia
- University Multiprofile Hospital for Active Treatment - Prof. Dr. Stoyan Kirkovich AD Department of Clinical Hematology — Stara Zagora
- Fakultní nemocnice Olomouc — Olomouc
California
- City of Hope - Duarte Main Site — Duarte
Maryland
- Maryland Oncology Hematology - Independent of SCRI/ US Oncology — Columbia
New York
- Weill Cornell Medicine NewYork-Presbyterian — New York
North Carolina
- Duke University — Durham
Ohio
- Cleveland Clinic — Cleveland
Texas
- MD Anderson — Houston
Utah
- Huntsman Cancer Institute — Salt Lake City
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 58 participants |
| Start Date | 2024-04-22 |
| Est. Completion | 2028-10 |
| Phase | Phase 2 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT05980806
The ClinicalTrials.gov registry entry for NCT05980806 describes a study currently listed as 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 58 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 3 conditions, with Myelofibrosis appearing as the primary indexed condition, and to 5 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: NCT05980806 reports 20 study locations spanning 13 distinct geographic areas — top geographies include Other, California, Maryland. 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 NCT05980806 about?
NCT05980806 is a clinical study titled "A Study of Selinexor Monotherapy in Subjects With JAK Inhibitor-naïve Myelofibrosis and Moderate Thrombocytopenia". The main purpose of this study is to evaluate the efficacy of selinexor in JAKi-naïve participants with myelofibrosis (MF) and with normal platelet counts or with mild to moderate thrombocytopenia based on spleen volume reduction (SVR). Additional efficacy and safety parameters will also be assessed...
What is the current status of trial NCT05980806?
This trial is currently recruiting. It is a Phase 2 study. The enrollment target is 58 participants. The study started on 2024-04-22. Estimated completion is 2028-10.
What conditions does trial NCT05980806 study?
This clinical trial studies the following conditions: Myelofibrosis, Moderate Thrombocytopenia, Mild Thrombocytopenia. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT05980806?
The interventions under investigation include: Ruxolitinib (DRUG), Momelotinib (DRUG), Pacritinib (DRUG), Selinexor 60 mg (DRUG), Selinexor 40 mg (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT05980806?
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 NCT05980806 being conducted?
This trial has 20 study locations across California, Maryland, New York, North Carolina, Ohio. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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