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 aged 18 to 75 years old, of any gender
- People who have been diagnosed (confirmed by tissue testing) with certain types of B-cell lymphoma, including diffuse large B-cell lymphoma (DLBCL), transformed follicular lymphoma, primary mediastinal B-cell lymphoma, mantle cell lymphoma (MCL), or other similar types that have converted from a slower-growing form
- People whose lymphoma has come back or stopped responding to treatment — the specific requirements depend on the type of lymphoma (confirm with trial site for your specific situation)
- People whose previous treatment included a type of drug called a CD20 antibody (unless their cancer cells do not carry the CD20 marker) and a type of chemotherapy called anthracyclines
- People who have at least one area of disease that can be measured on a scan, with the largest spot being at least 1.5 cm across
- People with an expected survival of at least 12 weeks
- People whose tumour tissue tests positive for a marker called CD19
- People with a general health/activity score of 0–2 on a standard medical scale (meaning able to carry out daily activities, with at most some limitations)
- People whose liver, kidney, and heart are functioning well enough to meet specific laboratory test thresholds (confirm details with trial site)
- People whose resting blood oxygen level is above 92% in normal indoor air
- People who have previously had a stem cell transplant
- People who have finished other anti-lymphoma treatments (such as chemotherapy, radiotherapy, or immunotherapy) at least 3 weeks before starting this trial
- People who previously received CAR-T cell therapy but whose treatment failed or whose disease came back at least 3 months after that therapy was assessed
- Women of childbearing age who have a negative pregnancy test and agree to use effective contraception during the trial
- People who have tested negative for COVID-19 and swine flu on two separate tests
Who may not be able to join:
- People who are allergic to any ingredient in the cell therapy product used in this trial
- People who have a history of any other cancer
- People who have had, or are currently being treated for, a serious immune reaction called graft-versus-host disease (GvHD) — specifically moderate to severe forms (Grade II–IV)
- People who received gene therapy within the past 3 months
- People who have an active infection currently requiring treatment (minor infections like simple urinary tract infections or bacterial throat infections may be acceptable — confirm with trial site)
- People who are infected with hepatitis B, hepatitis C, syphilis, HIV, or other conditions that weaken the immune system (some hepatitis B cases may still be considered — confirm with trial site)
- People with serious heart problems classified as Grade III or IV by a standard medical heart-function scale
- People who still have significant side effects from previous cancer treatment that have not recovered to a mild level (with the exception of tiredness, loss of appetite, or hair loss)
- People with a history of epilepsy or other conditions affecting the brain or nervous system
- People whose brain scans show signs that the lymphoma has spread to the central nervous system
- Women who are currently breastfeeding and unwilling to stop
- People who have any other condition or factor that the trial doctor believes could increase risk or affect the trial results
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: Wenbin Wenbin, Professor, Zhejiang University
Phone: +8613605801032
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 dose limiting toxicity (DLTs)
Can't join this trial?
Data last synced from ClinicalTrials.gov: 12 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.