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.
調査の概要
詳細な説明
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.
研究の種類
入学 (推定)
段階
- フェーズ2
- フェーズ 1
連絡先と場所
研究連絡先
- 名前:Eva Cerezo
- 電話番号:3214 91 5504800
- メール:eva.cerezo@quironsalud.es
研究連絡先のバックアップ
- 名前:Lucia Llanos
- 電話番号:3214 91 5504800
- メール:lucia.llanos@quironsalud.es
研究場所
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León、スペイン、24008
- まだ募集していません
- Hospital Universitario de León
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Madrid、スペイン、28040
- まだ募集していません
- Hospital Universitario Fundación Jiménez Diaz
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Murcia、スペイン、30120
- まだ募集していません
- Hospital Clínico Universitario Virgen de la Arrixaca
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Salamanca、スペイン、37007
- まだ募集していません
- Hospital Universitario de Salamanca
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Seville、スペイン、41013
- まだ募集していません
- Hospital Universitario Virgen del Rocio
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Barcelona
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Badalona、Barcelona、スペイン、08916
- まだ募集していません
- Hospital Germans Trias i Pujol
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Galicia
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Santiago de Compostela、Galicia、スペイン、15706
- まだ募集していません
- Hospital Clínico Universitario de Santiago
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Navarre
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Pamplona、Navarre、スペイン、31008
- 募集
- Clinica Universidad de Navarra
-
-
参加基準
適格基準
就学可能な年齢
健康ボランティアの受け入れ
受講資格のある性別
説明
Inclusion Criteria:
- Ability and willingness to provide written informed consent.
- 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.
- 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.
- 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.
- Evidence of refractory or treatment-resistant lupus nephritis according to GLOSEN criteria.
- Estimated glomerular filtration rate (eGFR) ≥30 mL/min/1.73 m² during the screening period.
- 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.
- 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.
- Adequate venous access and no contraindication to leukapheresis.
- 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.
- Completion of recommended vaccinations, including SARS-CoV-2 vaccination/immunization, before study treatment.
- Ability and willingness to comply with all study procedures and follow-up requirements.
Exclusion Criteria:
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Planned initiation of renal replacement therapy during the study period or eGFR <30 mL/min/1.73 m².
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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.
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Active infection requiring treatment during screening or before lymphodepletion.
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Positive screening for HIV, hepatitis C virus, hepatitis B virus, or evidence of active tuberculosis.
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Grade ≥2 thromboembolic event within 4 weeks before screening.
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History of progressive multifocal leukoencephalopathy (PML) or symptoms suggestive of PML.
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Requirement for systemic glucocorticoids at doses ≥30 mg/day prednisone equivalent.
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Previous treatment with anti-CD19 CAR-T therapy.
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Known hypersensitivity or contraindication to TranspoCART19, fludarabine, cyclophosphamide, bendamustine, or required concomitant medications.
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Concurrent systemic autoimmune disease requiring immunosuppressive therapy independent of SLE treatment.
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Current or previous malignancy, except adequately treated non-melanoma skin cancer, carcinoma in situ, or malignancy in complete remission for more than 3 years.
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Previous solid organ transplantation, hematopoietic stem cell transplantation, or bone marrow transplantation.
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Planned major surgery within one year after study treatment.
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Receipt of live vaccines within 30 days before administration of the investigational product.
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Current drug or alcohol abuse that may interfere with study participation.
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Any severe or uncontrolled medical or psychiatric condition that, in the investigator's opinion, would increase risk or interfere with study participation.
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Pregnancy or breastfeeding.
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Women of childbearing potential unwilling to use highly effective contraception throughout the study period.
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Sexually active men unwilling to use condoms and follow reproductive precautions required by the protocol.
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Participation in another interventional clinical trial within 90 days before informed consent or receipt of another investigational product within the protocol-specified washout period.
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Inability or unwillingness to provide informed consent or comply with study requirements.
研究計画
研究はどのように設計されていますか?
デザインの詳細
- 主な目的:処理
- 割り当て:なし
- 介入モデル:単一グループの割り当て
- マスキング:なし(オープンラベル)
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
|
実験的: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. |
この研究は何を測定していますか?
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Number of Participants With Adverse Events and Serious Adverse Events Following TranspoCART19 Infusion.
時間枠: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).
|
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Number of Participants Achieving Complete or Partial Clinical and Immunological Remission.
時間枠: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.
時間枠: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.
時間枠: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
時間枠: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.
時間枠: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.
時間枠: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
時間枠: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
時間枠: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
時間枠: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
時間枠: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
時間枠: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
時間枠: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
時間枠: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
時間枠: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
時間枠: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.
時間枠: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.
時間枠: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.
時間枠: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.
時間枠: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.
時間枠:Baseline through 24 months after infusion
|
Changes from baseline in LupusQoL scores. |
Baseline through 24 months after infusion
|
協力者と研究者
捜査官
- 主任研究者:Alberto Ortiz Arduan、Hospital Universitario Fundación Jiménez Díaz. IIS-FJD.
研究記録日
主要日程の研究
研究開始 (実際)
一次修了 (推定)
研究の完了 (推定)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (実際)
学習記録の更新
投稿された最後の更新 (実際)
QC基準を満たした最後の更新が送信されました
最終確認日
詳しくは
本研究に関する用語
キーワード
追加の関連 MeSH 用語
その他の研究ID番号
- CART-NEL
- ICI24/00034 (その他の助成金/資金番号:Instituto de Salud Carlos III)
- 2025-522449-23-00 (Ctis)
- 2025 (米国 NIH グラント/契約)
個々の参加者データ (IPD) の計画
個々の参加者データ (IPD) を共有する予定はありますか?
医薬品およびデバイス情報、研究文書
米国FDA規制医薬品の研究
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