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 @ 3:54 PM
Ignite Modification Date:
2025-12-24 @ 3:54 PM
NCT ID:
NCT04690192
Eligibility Criteria:
Key Inclusion Criteria:
1. Histologically confirmed large B-cell lymphoma including the following types
* diffuse large B-cell lymphoma
* high-grade B-cell lymphoma with or without MYC and BLC2 and/or BCL6 rearrangement
* transformed lymphoma
2. Relapsed or refractory diseases fulfilling one of the following criteria (individuals must have received anti-CD20 monoclonal antibody and anthracycline-containing chemotherapy regimen)
* Primary refractory disease, defined as disease progression after first-line immunochemotherapy or disease progression within 6 weeks of the end of the last chemotherapy
* Stable disease (SD) as best response after at least 4 cycles of first-line therapy
* Partial response (PR) as best response after at least 6 cycles of first-line therapy (biopsy-proven residual disease is needed for individuals with Deauville score of 4)
* PR as best response after at least 2 cycles of second-line therapy
* Disease relapse ≤12 months after the completion of first-line immunochemotherapy
* Relapsed or refractory disease after ≥2 lines of chemotherapy
3. Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1
4. Adequate bone marrow function as evidenced by:
* Absolute neutrophil count (ANC) ≥ 1000/uL
* Platelet count≥ 75,000/uL
5. Adequate renal and hepatic function defined as:
* Serum alanine aminotransferase (ALT/AST) ≤ 3 upper limit of normal (ULN)
* Total bilirubin ≤1.5 mg/dL, except in individuals with Gilbert's syndrome
* Serum creatinine ≤2 ULN, or creatinine clearance (as estimated by Cockcroft Gault) ≥ 40 mL/min
6. Cardiac ejection fraction ≥ 50%
7. Baseline oxygen saturation \> 92% on room air
8. Life expectancy ≥3 months
Key Exclusion Criteria:
1. Active Central Nervous System (CNS) involvement by lymphoma
2. History of autologous or allogeneic stem cell transplantation
3. Active HBV or HCV infection, defined as HBV-DNA or HCV-DNA levels above the normal upper limit, with or without abnormal liver function. Individuals with positive HBsAg or HBcAb should receive antiviral prophylaxis for at least 12 months after CNCT19 infusion.
4. Presence of uncontrolled infection, cardio-cerebrovascular disease，coagulopathy, or connective tissue disease.
5. History of seizure or other CNS disorder
6. History of HIV infection
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
65 Years
Study:
NCT04690192
Study Brief:
Protocol Section:
NCT04690192