A Prospective, Open-label and Single-arm Study of Anti-PD1 Armored CD19 CAR-T Cells in Adult Subjects With Relapsed or Refractory Diffuse Large B-cell Lymphoma

Status: Recruiting
Location: See location...
Intervention Type: Biological
Study Type: Interventional
Study Phase: Phase 1
SUMMARY

The purpose of this study is to investigate the safety and tolerability of anti-PD1 armored CD19 CAR-T Cells in adult subjects with relapsed or refractory diffuse large B-cell lymphoma.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
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• 1\. Subjects voluntarily participate in clinical research and sign informed consent.

• 2\. Adult subjects (age ≥18 ) with relapsed or refractory diffuse large B-cell lymphoma: a) failure to achieve CR after 6 cycles, or PR after 3 cycles, of first-line therapy, or achieve CR after first-line therapy but relapse within 12 months; b) achieve CR after systemic treatment, but are refractory or relapsed, and no plan to transplant, or prepare for transplantation but cannot meet transplantation criteria after second-line therapy; c) not achieve CR after at least two courses of second-line treatment (including autologous stem cell transplantation).

• 3\. Expected survival ≥ 3 months.

• 4\. At least one measurable lesion as per revised IWG response criteria for malignant lymphom (2014 Lugano criteria).

• 5\. CD19 positive expression are detected on tumor cells of subjects by flow cytometry or immunohistochemistry.

• 6\. ECOG score ≤ 2.

• 7\. Subjects with adequate organ functions prior to enrollment, meet the following laboratory values:

• Renal function: serum creatinine ≤ 1.5 × ULN or estimated glomerular filtration rate (eGFR) ≥ 60 mL/min/1.73 m².

• Hepatic function: Serum alanine aminotransferase (ALT) ≤ 5 × age-specific ULN and total bilirubin ≤ 2.0 mg/dL, except in subjects with Gilbert-Meulengracht syndrome. If total bilirubin ≤ 3.0 × ULN and direct bilirubin ≤ 1.5 × ULN, subjects with Gilbert-Meulengracht syndrome are included.

• Pulmonary reserve: ≤ Grade 1 dyspnea and oxygen saturation \>95% on room air.

• 8\. Stable hemodynamics and left ventricular ejection fraction (LVEF) ≥ 45 % assessed by echocardiography or multi-gated radionuclide angiography (MUGA).

• 9\. Adequate bone-marrow reserve without blood transfusion as defined by:

• Absolute neutrophil count (ANC) ≥ 1 x 10\^9/L.

• Absolute lymphocyte count (ALC) ≥ 0.1 x 10\^9/L.

• Platelets ≥ 50 x 10\^9/L.

• Hemoglobin \>80g/L.

• 10\. In the investigator's judgment, subjects' general condition and all biochemical values are either normal or sufficiently compensated to receive lymphodepletion and CAR-T cell therapy.

Locations
Other Locations
China
Suzhou Hongci Hematology Hospital
RECRUITING
Suzhou
Contact Information
Primary
Xiao Ma
colleenld2020@hotmail.com
0512-83837999
Time Frame
Start Date: 2026-01
Estimated Completion Date: 2029-01
Participants
Target number of participants: 30
Treatments
Experimental: Anti-PD1 armored CD19 CAR-T cells treatment arm
Subjects will be administrated with Anti-PD1 armored CD19 CAR-T cells after lymphocyte depletion by fludarabine and cyclophosphamide.
Sponsors
Leads: Jiangsu Topcel-KH Pharmaceutical Co., Ltd.

This content was sourced from clinicaltrials.gov

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