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:
- People who are willing to take part voluntarily and sign a consent form
- Adults aged 18 to 75, 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, or related types — and whose cancer has come back or stopped responding to previous treatments (specific treatment history requirements vary by lymphoma type — confirm with trial site)
- People who have at least one measurable area of disease that is 1.5 cm or larger
- People whose life expectancy, apart from their lymphoma, is estimated to be more than 12 weeks
- People whose lymphoma has previously tested positive for CD19 or CD70 markers
- People with a general health and activity level score (called ECOG status) of 0 to 3, meaning they range from fully active to limited in self-care (confirm with trial site)
- People whose liver, kidney, heart, and blood counts meet specific minimum levels of function as determined by blood tests and heart scans
- People who have previously had one autologous stem cell transplant (a procedure using their own stem cells)
- People who have waited the required time since their last treatment before receiving the study cell infusion (at least 3 weeks after chemotherapy or immunotherapy, or at least 2 weeks after targeted drug therapy alone)
- People whose previous CAR-T therapy has failed or whose disease came back at the 3-month assessment point
- People of childbearing or child-fathering potential who are willing to use birth control throughout the study, and women who can become pregnant must have a negative pregnancy test
- People who have tested negative for COVID-19 on two separate PCR or nucleic acid tests
Who may not be able to join:
- People who are allergic to any ingredient in the study cell product
- People who have had, or currently have, another type of cancer
- People who developed moderate to severe graft-versus-host disease (a complication from transplant) after a previous stem cell transplant, or who are still receiving treatment for it
- People who have had systemic gene therapy within the past 3 months
- People with an active, serious infection involving fungal, viral, or bacterial causes (though preventive infection treatments are permitted)
- People with a known history of hepatitis B (with certain virus levels), hepatitis C, syphilis, HIV, or other immune deficiency conditions
- People with severe heart failure classified as Class III or IV by standard medical criteria
- People still experiencing significant side effects (above a minor level) from previous treatments, with the exception of hair loss, tiredness, or reduced appetite
- People with a known history of active seizures, ongoing seizure activity, or other diseases affecting the brain or nervous system
- People whose scans (CT or MRI) show lymphoma affecting the brain or spinal fluid
- People who are currently breastfeeding
- People who, in the opinion of the trial doctor, have any other circumstances that could increase risk or affect the reliability of the study 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: aibin Liang, Shanghai Tongji Hospital, Tongji University School of Medicine
Phone: 18601670600
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: 21 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.