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 blood cancer called large B-cell lymphoma, confirmed through laboratory testing
- People whose large B-cell lymphoma has come back or stopped responding to treatment after at least two rounds of standard cancer treatment
- People whose treating doctor plans to use a CAR-T cell therapy product that has been approved by China's national medicine regulatory authority (the NMPA) for this type of lymphoma
- People who are willing and able to give written agreement to take part in the study. If a person is not able to make this decision independently, their legal guardian must give written agreement on their behalf
Who may not be able to join:
- People who the research team considers unlikely to follow the study's requirements and procedures
- People who are pregnant or currently breastfeeding
- People who have other conditions or circumstances that the research team considers unsuitable for participation in the study (confirm with trial site for details)
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: Chuan xu Liu, M.D, Fudan University
Phone: 021-64175590
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
explore predictors of CAR-T efficacy
Can't join this trial?
Data last synced from ClinicalTrials.gov: 28 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.