Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 4:27 PM
Ignite Modification Date:
2025-12-24 @ 4:27 PM
NCT ID:
NCT06646666
Eligibility Criteria:
Inclusion Criteria:
* Willingly sign the informed consent form.
* Age ≥ 18 years, any gender.
* Histologically confirmed as B-cell non-Hodgkin lymphoma, including:
* Diffuse large B-cell lymphoma (DLBCL) not otherwise specified (DLBCL-NOS)
* Transformed follicular lymphoma (tFL)
* High-grade B-cell lymphoma (HGBL) with MYC, BCL2, and/or BCL6 rearrangements
* High-grade B-cell lymphoma not otherwise specified (HGBL-NOS)
* Primary mediastinal large B-cell lymphoma (PMBL)
* Follicular lymphoma grade 3b (FL3b)
* Patients must have experienced at least one line of treatment for relapsed or refractory disease, meeting the following definitions:
* Refractory: At least partial response (PR) after the last chemotherapy or relapse within 12 months after autologous transplantation.
* Relapsed: Complete response (CR) after the last chemotherapy, followed by relapse before enrollment, or relapse or progression 12 months or longer after autologous transplantation.
* Maximum tumor diameter (long axis) \> 4 cm.
* Evaluator determines that the patient does not meet HDCT/ASCT criteria and meets at least one of the following:
* Age ≥ 60 years
* ECOG score = 2
* FEV1% or DLCO% ≤ 60%
* LVEF \< 50%
* Creatinine clearance \< 60 mL/min
* ALT or AST \> 2× upper limit of normal (ULN)
* Patient unwilling to receive high-dose chemotherapy and autologous stem cell transplantation.
* Measurable target lesions: lymph nodes ≥ 15 mm in longest diameter, or extranodal lesions \> 10 mm.
* Expected survival ≥ 12 weeks.
* Laboratory tests must meet the following requirements at screening:
* Lymphocyte count ≥ 0.1 × 10\^9/L
* Hemoglobin ≥ 80 g/L
* Platelets ≥ 50 × 10\^9/L
* ALT/AST ≤ 5 × ULN and total bilirubin \< 2 × ULN
* Creatinine clearance ≥ 30 mL/min
* Lung function: ≤ CTCAE grade 1 dyspnea, and oxygen saturation (SpO2) ≥ 92% in room air.
* LVEF ≥ 40%
* Patients with primary central nervous system lymphoma are allowed (secondary CNS lymphoma is not allowed).
* Sufficient venous access for apheresis, and no other contraindications for blood cell separation; female participants of childbearing potential must have a negative pregnancy test at screening.
Exclusion Criteria:
* History of allergy to any component of the cellular product or study treatment.
* History of allogeneic hematopoietic stem cell transplantation.
* History of organ transplantation.
* Patients with active viral hepatitis requiring treatment, including:
* Chronic HBV carriers with HBV DNA ≥ 500 IU/mL.
* Positive HCV RNA in patients with positive HCV antibodies.
* Positive HIV antibodies (HIV-Ab).
* Positive Treponema pallidum antibodies (TP-Ab).
* Elevated CMV DNA or EBV DNA above normal limits.
* Clinical significance of CNS diseases
* Presence of active primary central nervous system lymphoma.
* Prior treatment with other genetically modified T-cell therapies or CAR-T therapies.
* Severe genetic diseases or autoimmune diseases (e.g., systemic lupus erythematosus).
* Thromboembolic events (e.g., myocardial infarction, pulmonary embolism, deep vein thrombosis) within 6 months prior to screening.
* History of malignancies other than the indication for this trial within the last 5 years, except for in situ cancers (e.g., cervical, bladder, breast) or non-melanoma skin cancer.
* Active infections requiring systemic treatment or uncontrolled infections.
* Received lenalidomide, calcineurin inhibitors, chemotherapy (e.g., methotrexate, cyclophosphamide, ifosfamide, nitrogen mustard, or melphalan), mycophenolate, thalidomide, immunosuppressive antibodies (e.g., anti-TNF, anti-IL6, or anti-IL6R), radiation therapy, or any drug that binds FKBP12 (e.g., rapamycin, tacrolimus, everolimus) within 4 weeks prior to PBMC collection.
* Pregnant or breastfeeding women, or men or women of childbearing potential unwilling to use contraception during the trial and for 2 years after RJ CAR-T 002 cell infusion.
* Participation in other drug clinical trials (e.g., new drug trials, registrational studies, investigator-initiated trials) within 4 weeks prior to PBMC collection.
* Researcher's judgment that the patient is unsuitable for the trial (e.g., poor compliance, drug abuse).
* Vaccination with live or attenuated vaccines within 3 months prior to PBMC collection, or expected vaccination during the trial.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT06646666
Study Brief:
Protocol Section:
NCT06646666