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Study to Evaluate the Safety and Preliminary Efficacy of CD19 CAR-T Cell Therapy (TranspoCART19) in Patients With Refractory Lupus Nephritis (CART-NEL)

A National Multicenter Phase I/IIa Study to Evaluate the Safety and Preliminary Efficacy of CD19 CAR-T Cell Therapy (TranspoCART19) in Patients With Refractory Lupus Nephritis.

The goal of this clinical trial is to evaluate the safety and preliminary efficacy of CD19 CAR-T cell therapy (TranspoCART19) in adults with refractory lupus nephritis. Lupus nephritis is a serious kidney complication of systemic lupus erythematosus that may not respond adequately to standard treatments.

The main questions this study aims to answer are:

  • Is TranspoCART19 safe and tolerable in patients with refractory lupus nephritis?
  • Can TranspoCART19 induce complete or partial clinical and immunological remission?

Participants will:

  • Undergo leukapheresis to collect immune cells for manufacturing TranspoCART19.
  • Receive lymphodepleting chemotherapy before treatment.
  • Receive a single fractionated infusion of TranspoCART19.
  • Attend regular follow-up visits for safety, disease activity, kidney function, immune response, and quality-of-life assessments for up to 24 months, with long-term safety follow-up after study completion.

研究概览

地位

尚未招聘

详细说明

This is a Phase I/IIa, academic, multicenter, open-label, single-arm clinical trial designed to evaluate the safety, tolerability, and preliminary efficacy of TranspoCART19 in adult patients with refractory lupus nephritis.

TranspoCART19 is an autologous CD19-directed chimeric antigen receptor (CAR) T-cell therapy manufactured using Sleeping Beauty transposon technology. The CAR construct incorporates an anti-CD19 FMC63 single-chain variable fragment, a 4-1BB co-stimulatory domain, a CD3ζ signaling domain, and a truncated human epidermal growth factor receptor (hEGFRt) safety switch.

Eligible participants will undergo leukapheresis for collection of peripheral blood mononuclear cells. Following manufacturing of the investigational product, participants will receive lymphodepleting chemotherapy with fludarabine and cyclophosphamide, or bendamustine when clinically indicated, prior to administration of TranspoCART19.

TranspoCART19 will be administered intravenously at a target dose of 1 × 10^6 CAR-T cells/kg body weight using a fractionated infusion strategy consisting of 10%, 30%, and 60% dose fractions. Participants will remain under close monitoring for early and late treatment-related toxicities.

The primary objective is to evaluate the safety and tolerability of TranspoCART19 during the early post-infusion period. Safety assessments include adverse events, serious adverse events, cytokine release syndrome (CRS), immune effector cell-associated neurotoxicity syndrome (ICANS), severe infections, prolonged cytopenias, and hypogammaglobulinemia.

Secondary objectives include evaluation of clinical, renal, histological, and immunological responses; hematologic and immune reconstitution; CAR-T cell persistence and kinetics; corticosteroid and immunosuppressive treatment withdrawal; systemic lupus erythematosus disease activity; and health-related quality of life.

Approximately 10 participants will be enrolled. Participants will be followed for 24 months after infusion, and long-term safety monitoring will continue for up to 15 years in accordance with recommendations for genetically modified cellular therapies.

研究类型

介入性

注册 (估计的)

10

阶段

  • 阶段2
  • 阶段1

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习联系方式

研究联系人备份

学习地点

      • León、西班牙、24008
        • Hospital Universitario de Leon
      • Madrid、西班牙、28040
        • Hospital Universitario Fundación Jiménez Díaz
      • Murcia、西班牙、30120
        • Hospital Clínico Universitario Virgen de la Arrixaca
      • Salamanca、西班牙、37007
        • Hospital Universitario De Salamanca
      • Seville、西班牙、41013
        • Hospital Universitario Virgen del Rocío
    • Barcelona
      • Badalona、Barcelona、西班牙、08916
        • Hospital Germans Trías i Pujol
    • Galicia
      • Santiago de Compostela、Galicia、西班牙、15706
        • Hospital Clínico Universitario de Santiago
    • Navarre
      • Pamplona、Navarre、西班牙、31008
        • Clinica Universidad de Navarra

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

  • 成人
  • 年长者

接受健康志愿者

不

描述

Inclusion Criteria:

  1. Ability and willingness to provide written informed consent.
  2. Adults aged ≥18 and ≤65 years with a diagnosis of systemic lupus erythematosus (SLE) according to the 2019 European League Against Rheumatism/American College of Rheumatology (EULAR/ACR) classification criteria.
  3. Positive antinuclear antibody (ANA) result at a titer >1:80, or positive anti-double stranded DNA (anti-dsDNA), or positive anti-Smith (anti-Sm) antibodies at screening.
  4. Diagnosis of class III or IV proliferative lupus nephritis, with or without concomitant class V disease, confirmed by renal biopsy demonstrating active lupus nephritis according to the 2018 ISN/RPS classification.
  5. Evidence of refractory or treatment-resistant lupus nephritis according to GLOSEN criteria.
  6. Estimated glomerular filtration rate (eGFR) ≥30 mL/min/1.73 m² during the screening period.
  7. Urine protein-to-creatinine ratio (UPCR) >0.7 g/g, urine albumin-to-creatinine ratio (UACR) >0.5 g/g, proteinuria >0.7 g/24 h, or albuminuria >0.5 g/24 h at screening with evidence of active lupus nephritis.
  8. Stable treatment with an ACE inhibitor, angiotensin receptor blocker and/or mineralocorticoid receptor antagonist (with or without an SGLT2 inhibitor) for at least 3 months prior to screening, unless contraindicated or not tolerated.
  9. Adequate venous access and no contraindication to leukapheresis.
  10. Women of childbearing potential must have a negative pregnancy test at screening, prior to lymphodepletion and prior to infusion, and must agree to use highly effective contraception. Sexually active men must agree to use condoms and comply with protocol-specified reproductive precautions.
  11. Completion of recommended vaccinations, including SARS-CoV-2 vaccination/immunization, before study treatment.
  12. Ability and willingness to comply with all study procedures and follow-up requirements.

Exclusion Criteria:

  1. Planned initiation of renal replacement therapy during the study period or eGFR <30 mL/min/1.73 m².
  2. Severe organ dysfunction, including:

    • Left ventricular ejection fraction (LVEF) <40%.
    • Severe cardiac disease, including recent ischemic heart disease, NYHA class III-IV heart failure, uncontrolled arrhythmias, or severe lupus-related cardiac involvement.
    • Significant hepatic impairment (ALT or AST >1.5× ULN, total bilirubin >1.5× ULN except specified exceptions, INR >1.5).
    • Inadequate hematopoietic reserve (absolute neutrophil count ≤1000/µL, platelets <75,000/µL, leukocytes <3000/µL, lymphocytes ≤300/µL, hemoglobin <8 g/dL).
    • Oxygen saturation <92% on room air.
    • Severe pulmonary disease with compromised respiratory reserve.
  3. Active infection requiring treatment during screening or before lymphodepletion.
  4. Positive screening for HIV, hepatitis C virus, hepatitis B virus, or evidence of active tuberculosis.
  5. Grade ≥2 thromboembolic event within 4 weeks before screening.
  6. History of progressive multifocal leukoencephalopathy (PML) or symptoms suggestive of PML.
  7. Requirement for systemic glucocorticoids at doses ≥30 mg/day prednisone equivalent.
  8. Previous treatment with anti-CD19 CAR-T therapy.
  9. Known hypersensitivity or contraindication to TranspoCART19, fludarabine, cyclophosphamide, bendamustine, or required concomitant medications.
  10. Concurrent systemic autoimmune disease requiring immunosuppressive therapy independent of SLE treatment.
  11. Current or previous malignancy, except adequately treated non-melanoma skin cancer, carcinoma in situ, or malignancy in complete remission for more than 3 years.
  12. Previous solid organ transplantation, hematopoietic stem cell transplantation, or bone marrow transplantation.
  13. Planned major surgery within one year after study treatment.
  14. Receipt of live vaccines within 30 days before administration of the investigational product.
  15. Current drug or alcohol abuse that may interfere with study participation.
  16. Any severe or uncontrolled medical or psychiatric condition that, in the investigator's opinion, would increase risk or interfere with study participation.
  17. Pregnancy or breastfeeding.
  18. Women of childbearing potential unwilling to use highly effective contraception throughout the study period.
  19. Sexually active men unwilling to use condoms and follow reproductive precautions required by the protocol.
  20. Participation in another interventional clinical trial within 90 days before informed consent or receipt of another investigational product within the protocol-specified washout period.
  21. Inability or unwillingness to provide informed consent or comply with study requirements.

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:治疗
  • 分配:不适用
  • 介入模型:单组作业
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
实验性的:TranspoCART19
Participants with refractory lupus nephritis will undergo leukapheresis for manufacturing of autologous TranspoCART19 cells, followed by lymphodepleting chemotherapy and administration of TranspoCART19 as a fractionated intravenous infusion at a target dose of 1 × 10^6 CAR-T cells per kg.
Autologous CD19-directed CAR-T cell therapy administered following lymphodepleting chemotherapy. After leukapheresis and manufacturing, participants receive TranspoCART19 as a fractionated intravenous infusion (10%, 30%, and 60% of the target dose) at a total target dose of 1 × 10^6 CAR-T cells/kg body weight. The product is manufactured using Sleeping Beauty transposon technology and consists of genetically modified T lymphocytes expressing an anti-CD19 chimeric antigen receptor.

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Number of Participants With Adverse Events and Serious Adverse Events Following TranspoCART19 Infusion.
大体时间:Day 0 through Day 28 after infusion (extended through Day 42 for prolonged cytopenias).
Assessment of safety and tolerability based on the incidence and severity of adverse events, serious adverse events, unacceptable toxicity, cytokine release syndrome, immune effector cell-associated neurotoxicity syndrome, severe infections, prolonged cytopenias, and hypogammaglobulinemia.
Day 0 through Day 28 after infusion (extended through Day 42 for prolonged cytopenias).

次要结果测量

结果测量
措施说明
大体时间
Number of Participants Achieving Complete or Partial Clinical and Immunological Remission.
大体时间:Day 56 after TranspoCART19 infusion.
Proportion of participants achieving complete or partial clinical and immunological remission following TranspoCART19 infusion.
Day 56 after TranspoCART19 infusion.
Number of Participants With Adverse Events and Serious Adverse Events During Long-Term Follow-up.
大体时间:Baseline through Year 2
Incidence of adverse events, serious adverse events, vital sign abnormalities, physical examination findings, and laboratory abnormalities during long-term follow-up.
Baseline through Year 2
Change From Baseline in Hematopoietic and Immunological Reconstitution Parameters.
大体时间:Baseline through 24 months after infusion
Changes from baseline in hemoglobin, leukocyte count, platelet count, and immune cell subpopulations including CD3+, CD4+, CD8+, CD19+ B cells, CAR-T cells, NK cells, and NKT cells.
Baseline through 24 months after infusion
Number and Percentage of Circulating CD19 CAR-T Cells
大体时间:Baseline through 24 months after infusion
Number and percentage of circulating CD19 CAR-T cells in peripheral blood and their relationship with clinical response and adverse events.
Baseline through 24 months after infusion
Change From Baseline in Serum Immunological Activity Markers.
大体时间:Baseline through 24 months after infusion
Changes from baseline in ANA, anti-dsDNA, anti-histone, anti-SSA/Ro52, anti-SSB/La, anti-Sm, C3, C4, C1q, CH50, soluble BAFF, and total IgG levels.
Baseline through 24 months after infusion
Change From Baseline in Renal Disease Activity Parameters.
大体时间:Baseline through 24 months after infusion
Changes from baseline in estimated and measured glomerular filtration rate, microhematuria, proteinuria, albuminuria, and proportions of participants achieving complete or partial renal remission.
Baseline through 24 months after infusion
Change From Baseline in Renal Histological Disease Markers
大体时间:Baseline, Day 168, and Day 365
Changes in lupus nephritis activity index and chronicity indicators assessed by kidney biopsy, including immunohistochemical and immunofluorescence markers.
Baseline, Day 168, and Day 365
Time to Complete or Partial Renal Clinical Remission
大体时间:Baseline through 24 months after infusion
Time from TranspoCART19 infusion to achievement of complete or partial renal clinical remission.
Baseline through 24 months after infusion
Reduction or Discontinuation of Corticosteroids and Immunosuppressive Therapy
大体时间:Baseline through 24 months after infusion
Proportion of participants receiving prednisone doses of 5 mg/day or less or becoming free of immunosuppressive therapy and time required to achieve these outcomes.
Baseline through 24 months after infusion
Change From Baseline in Systemic Lupus Erythematosus Disease Activity
大体时间:Baseline through 24 months after infusion
Changes from baseline in SLEDAI-2K
Baseline through 24 months after infusion
Change From Baseline in Systemic Lupus Erythematosus Disease Activity
大体时间:Baseline through 24 months after infusion
Changes from baseline in BILAG-2004
Baseline through 24 months after infusion
Change From Baseline in Systemic Lupus Erythematosus Disease Activity
大体时间:Baseline through 24 months after infusion
Changes from baseline in Physician Global Assessment
Baseline through 24 months after infusion
Change From Baseline in Systemic Lupus Erythematosus Disease Activity
大体时间:Baseline through 24 months after infusion
Changes from baseline in SLE Flare Index
Baseline through 24 months after infusion
Change From Baseline in Systemic Lupus Erythematosus Disease Activity
大体时间:Baseline through 24 months after infusion
Changes from baseline in DORIS remission criteria.
Baseline through 24 months after infusion
Number of Participants Achieving Overall Treatment Response
大体时间:Day 365 after TranspoCART19 infusion.
Proportion of participants achieving overall treatment response defined as clinical remission, histological remission, and immunological remission.
Day 365 after TranspoCART19 infusion.
Change From Baseline in Health-Related Quality of Life.
大体时间:Baseline through 24 months after infusion
Changes from baseline in SF-36v2
Baseline through 24 months after infusion
Change From Baseline in Health-Related Quality of Life.
大体时间:Baseline through 24 months after infusion
Changes from baseline in EQ-5D-5L
Baseline through 24 months after infusion
Change From Baseline in Health-Related Quality of Life.
大体时间:Baseline through 24 months after infusion
Changes from baseline in FACIT-F
Baseline through 24 months after infusion
Change From Baseline in Health-Related Quality of Life.
大体时间:Baseline through 24 months after infusion
Changes from baseline in Patient Global Assessment
Baseline through 24 months after infusion
Change From Baseline in Health-Related Quality of Life.
大体时间:Baseline through 24 months after infusion
Changes from baseline in LupusQoL scores.
Baseline through 24 months after infusion

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

调查人员

  • 首席研究员:Alberto Ortiz Arduan、Hospital Universitario Fundación Jiménez Díaz. IIS-FJD.

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (估计的)

2026年9月1日

初级完成 (估计的)

2029年9月1日

研究完成 (估计的)

2030年9月1日

研究注册日期

首次提交

2026年8月25日

首先提交符合 QC 标准的

2026年8月28日

首次发布 (实际的)

2026年9月2日

研究记录更新

最后更新发布 (实际的)

2026年9月2日

上次提交的符合 QC 标准的更新

2026年8月28日

最后验证

2026年8月1日

更多信息

与本研究相关的术语

其他研究编号

  • CART-NEL
  • 2025 (美国 NIH 拨款/合同:Faculty of Social Sciences Scientific Grant at the University of Gdańsk)
  • ICI24/00034 (其他赠款/资助编号:Instituto de Salud Carlos III)
  • 2025-522449-23-00 (克蒂斯)

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

不

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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