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 signed a consent form agreeing to take part in the study
- Adults aged 18 or older
- People diagnosed with certain types of B-cell Non-Hodgkin Lymphoma (a cancer of the immune system), including large B-cell lymphoma, follicular lymphoma, mantle cell lymphoma, or marginal zone lymphoma, who have already tried at least 2 prior treatments and either tried or were not eligible for a specific type of immune cell therapy called CAR T cell therapy (specific prior treatment requirements differ by lymphoma type — confirm with trial site)
- People diagnosed with certain types of T-cell or NK-cell lymphoma (another group of immune system cancers) who have already received at least one prior treatment — some specific subtypes require two or more prior treatments (confirm with trial site)
- People diagnosed with classical Hodgkin Lymphoma where the cancer cells test positive for a marker called CD45, who have had at least 2 prior treatments including specific therapies, and in most cases a stem cell transplant (confirm with trial site)
- People whose chronic lymphocytic leukaemia (CLL) has transformed into a more aggressive lymphoma (called Richter's Transformation), who have had at least one prior treatment for that transformation or whose disease did not respond to initial treatment
- People whose doctor considers them suitable candidates for a type of stem cell transplant using their own cells
- People who previously had a donor stem cell transplant, provided it was more than 6 months ago, they have no active graft-versus-host disease (a condition where donor cells attack the body), and they are not taking medications to suppress the immune system
- People whose kidneys, liver, and heart are functioning at adequate levels as defined by specific test results (confirm with trial site)
- People whose lungs are functioning adequately, with oxygen levels above 92% on room air and no more than mild breathlessness
- People who are generally well enough to carry out normal daily activities with little or no limitation (as measured by a standard medical scale)
Who may not be able to join:
- People with an active hepatitis B or hepatitis C infection
- People with any active infection that is not under control
- People with serious heart failure classified as Class III or IV (meaning significant limitations on physical activity)
- People with an irregular heartbeat that has not been stable with medication within the two weeks before the doctor confirms eligibility
- People with serious other health conditions that, in the treating doctor's judgement, would make participation unsafe
- People with another cancer whose history or required treatment could interfere with the assessment of this trial's treatment
- People with active graft-versus-host disease (a complication from a prior donor stem cell transplant) that requires treatment
- People who are currently dependent on steroid medications or other immune-suppressing drugs
- People with lymphoma that is currently active in the central nervous system (brain or spinal cord) — people who had this previously but were successfully treated may still be considered eligible
- People whose blood tests show signs of a T-cell cancer circulating in the bloodstream
- People with a known allergy or sensitivity to any of the ingredients in the study treatment, including human serum albumin, DMSO, or Dextran 40
- People with an active autoimmune disease requiring immune-suppressing treatment at or above a certain dose level, or people with autoimmune conditions affecting the nervous system (such as multiple sclerosis)
- People who are pregnant or breastfeeding — people who are able to become pregnant must agree to use an acceptable form of contraception during the trial
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: Noelle Frey, MD, University of Pennsylvania
Phone: 215-349-8245
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
Incidence of Adverse Events as assessed by CTCAE v6.0; Occurrence of dose-limiting toxicities (DLTs); Identification of the maximum tolerated dose (MTD); Identification of a recommended dose for expansion (RDE)
Can't join this trial?
Data last synced from ClinicalTrials.gov: 15 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.