Phase 2 Lymphoma Trial, Recruiting NCT07356245 Sponsor: Jonathan Brammer Condition: Lymphoma
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Phase 2 Lymphoma Trial, Recruiting

NCT07356245
Recruiting Phase 2

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.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 16 July 2026
Phase 2: approximately ~30% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

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

Status
Recruiting
Phase
Phase 2
Sponsor
Jonathan Brammer
Registry
ClinicalTrials.gov
Start date
12 February 2026
Est. completion
31 December 2026

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Cumulative Incidence (CI) of relapse; GvHD and relapse free-survival (GRFS)

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

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.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov