Ireland
--:--IST
Recruiting Phase 1/2

Efficacy and Safety Evaluation of U01(ssCART-19) in B-Cell Lymphoma

NCT06987916 · tracked via the Priya Life Science China tracker
Phase
Phase 1/2
Started
2025-04-22
Last updated
2025-06-05

Condition(s) studied

B Cell Lymphoma

Investigational drug(s) / intervention(s)

ssCART-19 →

ssCART-19: autologous T cells transduced with a lentiviral vector containing anti-CD19 CAR and small hairpin RNA to silence the IL-6 gene

Study summary

This is an open-label phase1 study to assess the safety and efficacy of U01(ssCART-19) cell therapy in the treatment of patients with refractory or recurrent B-cell lymphoma .

Eligibility

Sex
ALL
Min age
2 Years
Max age
75 Years
Healthy volunteers
No
Inclusion Criteria: 1. Participants must voluntarily sign the informed consent form (ICF) and demonstrate good compliance. 2. Participants must meet the following requirements: 1. Age ≥2 years and ≤75 years at the time of signing the ICF (both sexes eligible). For minors (\<18 years), the legal guardian must sign after full disclosure; minors with decision-making capacity must co-sign with their guardians. 2. Confirmed diagnosis of B-cell lymphoma according to the NCCN Clinical Practice Guidelines for B-Cell Lymphomas (3rd Edition, 2024) . 3. Prior treatment requirements : Failure to achieve partial response (PR) after first-line therapy, or relapse within 12 months post-first-line therapy; Relapsed/refractory B-cell lymphoma after second-line therapy (one standard chemotherapy regimen + one salvage regimen). Prior treatments must include CD20 monoclonal antibody (unless CD20-negative tumor confirmed by the investigator) and anthracycline-based regimens . Additionally, meet one of the following: i. Ineligible for autologous stem cell transplantation (ASCT); ii. Refusal of ASCT; iii. Post-ASCT relapse. d) Refractory/relapsed status at screening: Relapse: Disease progression (PD) after achieving PR or complete response (CR); Refractory: i. No response to last-line therapy (PD during/after treatment, or stable disease \[SD\] lasting \<6 months); ii. Post-ASCT relapse/PD (biopsy-confirmed), including relapse/PD within 12 months post-ASCT with SD/PD after salvage therapy2. 3. CD19 positivity confirmed by immunohistochemistry (IHC) of tumor tissue (preferably within 6 months). 4. At least one measurable lesion assessed by the Lugano Lymphoma Response Criteria (Cheson 2014) . 5. ECOG performance status score 0-3 . 6. Adequate bone marrow reserve at screening: Absolute lymphocyte count (ALC) ≥0.3×10⁹/L ; Platelet count (PLT) ≥30×10⁹/L . 7. Adequate organ function: AST/ALT ≤3×ULN (≤5×ULN if due to tumor infiltration); Total bilirubin ≤2×ULN (≤3×ULN for Gilbert syndrome with direct bilirubin ≤1.5×ULN); Serum creatinine ≤1.5×ULN or creatinine clearance ≥60 mL/min (Cockcroft-Gault formula); Oxygen saturation \>91% on room air (dyspnea grade ≤1); Left ventricular ejection fraction (LVEF) ≥50% ; INR ≤1.5×ULN and APTT ≤1.5×ULN . 8. Negative pregnancy test (blood/urine) within 7 days before CAR-T infusion for women of childbearing potential. All participants must agree to use effective contraception during the study and for ≥1 year post-treatment. 9. Adequate venous access for leukapheresis or blood collection, with no contraindications to leukapheresis. 10. Expected survival ≥3 months . Exclusion Criteria: 1. Concurrent malignancies , except for: Malignancies with disease-free survival (DFS) \>3 years ; Carcinoma in situ ; 2. Active viral infections : Hepatitis B : Positive for HBe-Ab and/or HBc-Ab with HBV-DNA \> lower limit of quantitation (LLOQ) ; Hepatitis C : Positive HCV-Ab with HCV-RNA \> LLOQ ; Positive Treponema pallidum antibody (TP-Ab); Positive HIV antibody ; 3. Uncontrolled infections (bacterial, fungal, viral, mycoplasmal, or others) as determined by the investigator; 4. Clinically significant CNS diseases (current or history), including: Epilepsy, cerebrovascular ischemia/hemorrhage, dementia, cerebellar disorders, or CNS-related autoimmune diseases , deemed uncontrolled by the investigator; 5. Cardiovascular exclusion criteria : Cardiac angioplasty/stent placement within 12 months prior to signing ICF ; NYHA Class II-IV congestive heart failure , myocardial infarction, unstable angina, or other clinically significant cardiac history; QTe interval ≥480 ms (Fridericia correction) or LVEF \<50% at screening; 6. Primary immunodeficiency ; 7. Severe immediate hypersensitivity to any study drug; 8. Live vaccine administration within 6 weeks prior to screening ; 9. Pregnancy or lactation ; 10. Active autoimmune diseases ; 11. Participation in another interventional clinical trial within 30 days prior to ICF signing ; 12. Other conditions deemed ineligible by the investigator.

Primary outcome measure(s)

  • The types, frequency, and severity of treatment related adverse events — Day1 to Week 4
    After CAR-T cell infusion, we will observe the potential adverse events, especially Cytokine Release Syndrome(CRS) and neurotoxicity Using NCI Common Terminology Criteria for Adverse Events(CTCAE) V5.0
  • Objective response rate(ORR) — At 1,3,6,9,12,18 and 24 months post-treatment follow up
  • Duration of response (DOR) — At 1,3,6,9,12,18 and 24 months post-treatment follow up
  • Progression free survival(PFS) — At 1,3,6,9,12,18 and 24 months post-treatment follow up
  • Overall survival(OS) — At 1,3,6,9,12,18 and 24 months post-treatment follow up

Trial sites (1)

FacilityCityRegionStatus
Shanghai Tongji Hospital ( Tongji Hospital of Tongji University) Shanghai Shanghai Municipality Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06987916 on ClinicalTrials.gov ↗ ← All trials in China