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Study of Abexinostat in Patients With Relapsed or Refractory Follicular Lymphoma
NCT03600441 · View on ClinicalTrials.gov ↗
Study Summary
This study in patients with relapsed/refractory follicular lymphoma who have undergone at least 3 lines of therapy. Patients will receive abexinostat 80 mg (4 × 20 mg tablets) twice a day (BID) in a "one week on, one week off" schedule.
Conditions Studied
Interventions
- DRUG Abexinostat
Study Locations (15)
Other
- Hospital Universitario Vall d'Hebrón — Barcelona
- Hospital del Mar — Barcelona
- C.H. Regional Reina Sofia — Córdoba
- Hospital Universitario Infanta Leonor — Madrid
New York
- Clinical Research Alliance Inc — Lake Success
- Manhattan Hematology Oncology Center — New York
- Memorial Sloan Kettering Cancer Center — New York
Texas
- Arlington Cancer Center — Arlington
- Central Texas Veterans Health Care System - NAVREF — Temple
Illinois
- Advocate Medical Group - Park Ridge, Luther Lane - Oncology — Park Ridge
Kentucky
- Norton Cancer Institute - St. Matthews Campus — Louisville
Pennsylvania
- Bone Marrow Transplant Hematology Oncology Associates — Pittsburgh
Washington
- Vista Oncology Inc. PS — Olympia
Pyrénées-Orientales
- Centre Hospitalier de Perpignan — Perpignan
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 139 participants |
| Start Date | 2018-08-27 |
| Est. Completion | 2029-12-31 |
| Phase | Phase 2 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03600441
The ClinicalTrials.gov registry entry for NCT03600441 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 139 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Xynomic Pharmaceuticals, which has 2 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 Follicular Lymphoma appearing as the primary indexed condition, and to 1 intervention — of which Abexinostat 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: NCT03600441 reports 15 study locations spanning 9 distinct geographic areas — top geographies include Other, New York, Texas. 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 NCT03600441 about?
NCT03600441 is a clinical study titled "Study of Abexinostat in Patients With Relapsed or Refractory Follicular Lymphoma". This study in patients with relapsed/refractory follicular lymphoma who have undergone at least 3 lines of therapy. Patients will receive abexinostat 80 mg (4 × 20 mg tablets) twice a day (BID) in a "one week on, one week off" schedule.
What is the current status of trial NCT03600441?
This trial is currently active not recruiting. It is a Phase 2 study. The enrollment target is 139 participants. The study started on 2018-08-27. Estimated completion is 2029-12-31.
What conditions does trial NCT03600441 study?
This clinical trial studies the following conditions: Follicular Lymphoma. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT03600441?
The interventions under investigation include: Abexinostat (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT03600441?
This trial is sponsored by Xynomic Pharmaceuticals, which has 2 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT03600441 being conducted?
This trial has 15 study locations across Illinois, Kentucky, New York, Pennsylvania, Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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