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NCT06027957CompletedPhase 1

CD19 CAR T-Cell Therapy for R/R Non-Hodgkin Lymphoma and Acute Lymphoblastic Leukemia

Phase I Clinical Trial Evaluating the Safety and Efficacy of Point-of-care CAR-T-cell Therapy in the Treatment of Relapsed/Refractory CD19+ Non-Hodgkin Lymphoma and Acute Lymphoblastic Leukemia

Source: ClinicalTrials.gov · Last updated 26 Aug 2025

Brief summary (registry, in English)

* Brief Summary: Cluster of differentiation 19 (CD19) is expressed on B cells. CD19+ tumor cells in patients with non-Hodgkin lymphoma and acute lymphoblastic leukemia can be targeted using T cells expressing CD19-specific chimeric antigen receptor (CAR). * Objective: This study aims to evaluate the safety and efficacy of single-dose anti-CD19 CAR T-cell therapy in the treatment of relapsed/refractory CD19+ non-Hodgkin lymphoma and acute lymphoblastic leukemia. * Eligibility: People aged 1 to 60 years with relapsed/refractory CD19+ non-Hodgkin lymphoma and acute lymphoblastic leukemia. * Design: Phase 1 clinical trial, uncontrolled, single dose of CD19 CAR T-cells.

Status (registry)
Completed
Phase (registry)
Phase 1
Study type
Interventional
Enrollment
18 (actual)
First submitted
28 Jul 2023
Start date
2 Aug 2023
Primary completion date
30 Jun 2025
Lead sponsor
Vinmec Research Institute of Stem Cell and Gene Technology
NCT number
NCT06027957

What you commit to

  • Study type: Interventional · Phase 1
  • Participants enrolled: 18
  • From 2 Aug 2023 to the primary completion date, 30 Jun 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Receiving immunosuppressive medication, except for ≤ 30 mg prednisolone or equivalent at the time of CAR-T-cell transfusion.
  • Having other severe concomitant diseases (e.g., uncontrolled arterial hypertension, heart failure NYHA III-IV).
  • Unstable angina within 3 months prior to screening.
  • Any previous or concurrent malignancy was not B-cell lymphoma or B-ALL.

Other illness

  • Medical history of veno-occlusive disease (VOD).
  • Required acute treatment due to tumors such as intestinal obstructions, vascular compression, or respiratory failure.
  • Medical history of autoimmune neurological diseases or neuromyelitis.
  • Having acute, progressive, or chronic graft-versus-host disease (GvHD).
  • Patients who are critically ill or at risk of premature death characterized by:
    • Acute liver failure requiring dialysis
    • Heart failure requiring vasopressors
    • Systemic infection unresponsive to antibiotics
    • ECOG performance status ≥ 3 points at the time of screening
  • Medical history of clinically relevant central nervous system disease, such as epilepsy, convulsions, paralysis, aphasia, uncontrolled cerebrovascular disease, traumatic brain injury, and Parkinson's disease.
  • Other diseases or other conditions and circumstances that, according to the investigator's assessment, make it difficult to ensure compliance with study treatment.

Lab values

  • Having active infectious diseases determined by clinical, imaging, or other laboratory tests (blood culture, PCR, etc.)

Other

  • Involved central nervous system invasion at the time of screening.
  • Having active hemolytic anemia.
  • Diagnosed with primary immunodeficiency.
  • Intolerance to excipients from cellular products.
  • Pregnant women or those who expect to be pregnant or reastfeeding.
  • Participation in another clinical trial at the time of screening

Who the study is looking for

  • B-cell acute lymphoblastic leukemia: refractory to two cycles of chemotherapy, relapsed after chemotherapy, or hematopoietic stem cell transplantation.
  • B-cell non-Hodgkin lymphoma: refractory to two lines of chemotherapy, relapsed after chemotherapy, or hematopoietic stem cell transplantation.
  • Age: From 1 to 60 years old (both males and females)
  • Adequate organ functions:
    • Serum creatinine ≤ 1.5 x ULN or eGFR ≥ 60 mL/min/1.73 m2
    • ALT and AST ≤ 5 x ULN; Bilirubin ≤ 2.0 mg/dl
    • No chronic lung diseases, such as obstructive pulmonary disease or bronchial asthma, required continuous medications without respiratory failure (SpO2 oxygen saturation \> 92% at room temperature).
    • No arrhythmia, no intracardiac thrombus or vascular wall, no heart failure, LVEF ≥ 45%
  • Blood test:
    • Absolute neutrophil count (ANC) ≥ 1,000/mm3 (1 G/l) without filgrastim
    • Absolute lymphocyte count ≥ 100/mm3 (0.1 G/l)
    • Absolute platelet count ≥ 75,000/mm3 (75 G/l)
    • Hemoglobin ≥ 8.0 g/dl
  • Positive for CD19 measured by immunohistochemistry or flow cytometry.
  • Agree to participate in the study
  • Agree to use safe methods of contraception for female patients.

Age in the registry: 1 year to 60 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Vinmec Research Institute of Stem Cell and Gene Technology
Coordinator of this site? Confirm its status
HanoiVietnamUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.