Ruxolitinib after Stem Cell Transplant for T-cell Lymphoma

This study is testing if ruxolitinib, a medication, can help prevent T-cell lymphoma from coming back and reduce graft-versus-host disease (GVHD) after a stem cell transplant. GVHD happens when the donor cells attack your body. Ruxolitinib works by calming down the immune system and blocking cancer cell growth. We are looking for adults (18 and older) with T-cell lymphoma who are in partial or complete remission after their stem cell transplant. The main goals are to see how well ruxolitinib prevents relapse and improves survival without GVHD or relapse one year after the transplant. The study status is currently unclear, and we plan to enroll 44 participants.

Study design
This is an interventional study, but the phase is not specified. It plans to enroll 44 participants.
What's involved
You would take ruxolitinib orally twice daily. You would also undergo PET-CT scans, bone marrow biopsies, tissue biopsies, and blood sample collections.
Compensation
Not stated in the trial record.
Follow-up
The study measures outcomes at 1-year post-transplant, suggesting follow-up for at least that duration.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT07356245

Ruxolitinib Maintenance Post-Hematopoietic Stem Cell Transplant T-Cell Lymphoma

Recruiting
PHASE2Ages 18+InterventionalTreatment
Jonathan Brammer
~44 participants
Updated 2026-04-15 on ClinicalTrials.gov
What's tested:RuxolitinibPositron emission tomography-computed tomographyBone Marrow BiopsyBiopsy ProcedureBiospecimen Collection

At a glance

Recruiting sites
1 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Cumulative Incidence (CI) of relapse
Measured over at 1-year post-auto-SCT
+1 more outcome measured
T-cell Lymphoma
Graft Versus Host Disease
Lymphoma, T-Cell
Peripheral T Cell Lymphoma
T-cell Prolymphocytic Leukemia
Cutaneous T Cell Lymphoma
Adult T-cell Leukemia/Lymphoma
Primary Cutaneous T-Cell Non-Hodgkin Lymphoma

NCT07356245

Where you'd take part

This study runs at 1 site. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.

  • Ohio State University Comprehensive Cancer Center

    Columbus, Ohiostudy coordinator listed

    Recruiting

Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.

  • Jonathan Brammer, MD · PRINCIPAL_INVESTIGATOR · Ohio State University Comprehensive Cancer Center
The Ohio State University Comprehensive Cancer Center
Email the study team

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  • Cumulative Incidence (CI) of relapseat 1-year post-auto-SCT

    Relapse is defined as evidence of disease progression or recurrence based on Lugano criteria or confirmed by biopsy.

  • GvHD and relapse free-survival (GRFS)at 1-year post-allo-SCT

    GRFS is a composite endpoint of survival without grade III-IV acute GVHD, systemic therapy-requiring chronic GVHD (cGVHD), relapse, or death. Will be evaluated using the Kaplan-Meier method, with median survival and probability of surviving to relevant time points reported with point estimates and 90% confidence intervals separately for each study cohort. Comparisons to Center for International Blood and Marrow Transplant Research (CIBMTR) patients will use log-rank tests.