Phase 2 Lymphoma Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- You are an adult diagnosed with a type of T-cell lymphoma (including PTCL, T-PLL, ATLL, or CTCL of any subtype) and your cancer is in partial or complete remission between 35 and 120 days after a stem cell transplant (either from your own cells or a donor's cells)
- You are generally well enough to carry out light activity and care for yourself (a doctor will assess this using a standard scale)
- Your blood counts are at an acceptable level — including white blood cells, platelets, and red blood cells — without needing supportive injections or transfusions for at least 3 days
- Your liver, kidneys, and lungs are functioning well enough based on blood and oxygen tests
- You are able to swallow and digest medication taken by mouth or through a feeding tube
- You agree to use an effective form of birth control throughout the study (if you are a woman who could become pregnant or a man who could father a child)
- You are able to read and sign a consent form agreeing to take part in the study
Who may not be able to join:
- You have a specific subtype of lymphoma called ALK-positive or DUSP22-positive ALCL with a low risk score and are in your first complete remission
- Your cancer has gotten worse after the transplant, or you have received any other cancer treatment after the transplant (radiation therapy is allowed)
- Your cancer previously got worse while you were being treated with a drug called Ruxolitinib
- You have a transplant-related immune complication called graft-versus-host disease (GvHD) that requires treatment with systemic medications
- You have an active infection that is not under control
- You have an active blood vessel clotting condition that requires treatment (confirm with trial site)
- You have had a liver complication called veno-occlusive disorder after your transplant
- You are taking blood thinners or anti-clotting medications that cannot safely be stopped if your platelet levels drop
- You have a history of a life-threatening bleed, meaning one that required surgery or affected your brain or spinal cord
- You are pregnant or currently breastfeeding (pregnancy testing may be required if applicable)
- You have an uncontrolled infection with Hepatitis B, Hepatitis C, HIV, tuberculosis, or certain fungal infections
- You have taken part in another clinical trial or received an experimental drug within the past 4 weeks
- You have had a serious side effect from your stem cell transplant (rated severe or worse) that has not improved sufficiently
- You have had a heart attack or stroke within the past year
- You have any other uncontrolled health condition that the trial doctor feels would put you at risk
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Jonathan Brammer, MD, Ohio State University Comprehensive Cancer Center
Phone: 1-800-293-5066
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Cumulative Incidence (CI) of relapse; GvHD and relapse free-survival (GRFS)
Can't join this trial?
Data last synced from ClinicalTrials.gov: 16 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.