Clinical trial · Interventional
CNCT19 Following ASCT in Patients With Relapsed or Refractory B-cell Lymphoma
CNCT19 Following Autologous Stem Cell Transplantation in Patients With Relapsed or Refractory Aggressive B-cell Lymphoma
NCT04690192CI-TRIAL-00089619completedPhase 1 / Phase 2ClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
The primary objective of this study is to explore the safety and efficacy of CNCT19 (a second-generation anti-CD19 CAR T-cell using 4-1BB as co-stimulatory domain provided by Juventas, Tianjin, China) infusion following ASCT in patients with relapsed or refractory B-cell lymphoma.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Large B-cell Lymphoma | — | UNRESOLVED | — |
Interventions
Interventions (4)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| busulfan | Drug | Busulfan | ALIAS |
| CNCT19 | Biological | — | UNRESOLVED |
| Gemcitabine Injection | Drug | Gemcitabine | ALIAS |
| Melphalan Injection | Drug | Melphalan | ALIAS |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- CNCT19 following ASCT
- description
- Participants will receive high-dose chemotherapy followed by stem-cell reinfusion, and a fixed dose of CNCT19 (2×10\^6/kg) will be infused in a single-dose on day +2, +3 or +4.
- interventionNames
- Biological: CNCT19
- Drug: Gemcitabine Injection
- Drug: busulfan
- Drug: Melphalan Injection
Primary outcomes (1)
- measure
- Percentage of participants experiencing adverse events
- timeFrame
- from the first day of high-dose chemotherapy until 2 years post CNCT19 infusion
Secondary outcomes (6)
- measure
- Complete Response (CR) Rate
- timeFrame
- 2 years post CNCT19 infusion
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
- Maximum age
- 65 Years
Show eligibility criteria text
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
References
Publications (1)
- DERIVEDLiu W, Liu W, Zou H, Chen L, Huang W, Lv R, Xu Y, Liu H, Shi Y, Wang K, Wang Y, Xiong W, Deng S, Yi S, Sui W, Peng G, Ma Y, Wang H, Lv L, Wang J, Wei J, Qiu L, Zheng W, Zou D. Combinational therapy of CAR T-cell and HDT/ASCT demonstrates impressive clinical efficacy and improved CAR T-cell behavior in relapsed/refractory large B-cell lymphoma. J Immunother Cancer. 2024 Apr 16;12(4):e008857. doi: 10.1136/jitc-2024-008857. PMID 38631712