Phase 1 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:
- People who have been diagnosed with a type of cancer called non-Hodgkin lymphoma, confirmed by a tissue test, where the disease has come back after at least 2 previous treatments, has not responded to chemotherapy, or has returned within 12 months after a stem cell transplant using their own cells.
- People who do not have lymphoma affecting the brain or spinal cord.
- People who are older than 18 years of age.
- People whose general health and ability to carry out daily activities meets a specific medical fitness standard (confirm with trial site).
- People who have at least one measurable area of disease that can be tracked during the trial.
- People who have finished radiation therapy or other cancer treatment at least 2 weeks before the blood collection procedure used in this trial.
- People whose liver function test results fall within acceptable ranges, except in cases of a specific liver condition called Gilbert's syndrome.
- People whose kidney function test results fall within acceptable ranges.
- People whose heart is pumping effectively (above 50% efficiency), with no fluid build-up around the heart, as confirmed by a heart scan.
- People whose lungs are functioning adequately, as measured by blood oxygen levels of 92% or higher while breathing normal air.
- People (or their legal guardians) who are able to understand and willing to sign a written consent form.
- Women who could become pregnant must agree to either abstain from heterosexual intercourse or use a highly effective form of contraception during treatment and for at least 90 days after the treatment infusion.
- Men must agree to either abstain from heterosexual intercourse or use contraception, and must agree not to donate sperm during this period.
Who may not be able to join:
- People who have had a stem cell transplant using their own cells within the past 6 weeks.
- People who have previously had a stem cell transplant using cells from another person (a donor).
- People who currently have an active complication from a donor transplant known as graft-versus-host disease.
- People who have active lymphoma or leukaemia involvement in the brain, spinal cord, or surrounding membranes.
- People who currently have another active cancer, other than certain minor skin cancers or very early-stage cancers that have not spread.
- People who received an experimental treatment less than 28 days before the blood collection procedure for this trial.
- People with a severe form of heart failure classified as the most serious category (New York Heart Association Class IV).
- People who have had a serious heart or blood vessel event — such as a heart attack, stroke, unstable chest pain, or significant irregular heartbeat — within the past 6 months.
- People who currently have an active infection that requires treatment through a drip (intravenous antibiotics or antifungals).
- People who are HIV positive.
- People who are pregnant or breastfeeding.
- People who have signs of a certain type of bone marrow disorder called myelodysplasia, detected on a bone marrow test.
- People who have an active hepatitis B or hepatitis C infection.
- People who have a significant history of neurological conditions affecting the brain, such as epilepsy, uncontrolled seizures, stroke-related complications, severe brain injury, dementia, or Parkinson's disease.
- People who have another illness that is not currently under control.
- People who have another type of cancer that currently requires systemic treatment.
- People who have a history of an autoimmune disease and have needed immunosuppressive medications (other than low-dose steroids) within the past 6 months.
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: Paolo F. Caimi, MD, Cleveland Clinic Taussig Cancer Institute
Phone: 216 445-4635
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
To determine recommended phase II dose of human LMY-920.
Can't join this trial?
Data last synced from ClinicalTrials.gov: 14 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.