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CD19/BCMA-Targeted Universal CAR-T Cell Injection for the Treatment of Autoimmune Diseases

2026年7月15日 更新者:Nanjing Bioheng Biotech Co., Ltd.

Clinical Study on the Safety, Efficacy and Pharmacokinetics of Universal CD19/BCMA-Targeted CAR-T Cell Injection in Patients With Autoantibody-Mediated Autoimmune Diseases

This is a single-arm, open-label, investigator-initiated trial (IIT) designed to evaluate the safety, tolerability, pharmacokinetics, pharmacodynamics and efficacy of RD06-05 in patients with autoantibody-mediated autoimmune diseases. The enrolled population consists of patients with active autoimmune diseases, including systemic lupus erythematosus (SLE), systemic sclerosis (SSc), ANCA-associated vasculitis (AAV), idiopathic inflammatory myopathies (IIM), Sjögren's syndrome (SS), among others.

The CAR-T cell dose used in this study is 6×10⁶ CAR⁺ T cells/kg. Six subjects will be enrolled for each indication, with a total of 30 subjects to be enrolled.

調査の概要

研究の種類

介入

入学 (推定)

30

段階

  • 初期フェーズ 1

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究連絡先

研究場所

    • Shanghai Municipality
      • Shanghai、Shanghai Municipality、中国、220127
        • Renji Hospital Affiliated to Shanghai Jiao Tong University School of Medicine
        • コンタクト:

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

  • 大人
  • 高齢者

健康ボランティアの受け入れ

いいえ

説明

Inclusion Criteria

  1. General Inclusion Criteria (All Patients)

    1. Voluntarily provides written informed consent.
    2. Age ≥18 and ≤70 years, any gender.
    3. Adequate organ function:

      • ALT and AST ≤3×ULN; total bilirubin ≤2×ULN (excluding Gilbert syndrome).
      • Creatinine ≤1.5×ULN or creatinine clearance ≥40 mL/min.
      • Neutrophils ≥1×10⁹/L; hemoglobin ≥60 g/L; platelets ≥20×10⁹/L; lymphocytes >0.3×10⁹/L.
      • INR ≤1.5×ULN or PT ≤1.5×ULN.
      • Resting room-air SpO₂ ≥92%.
      • LVEF ≥50% on echocardiogram.
    4. Negative serum or urine pregnancy test for females of childbearing potential at screening.
    5. Highly effective contraception required from 28 days before lymphodepletion until 12 months after RD06-05 infusion for females; effective barrier contraception required from lymphodepletion until 12 months after RD06-05 infusion for males, with no sperm donation during the study.
  2. For SLE Patients

    1. Diagnosis of SLE per 2019 EULAR/ACR or 2012 SLICC criteria.
    2. Active disease despite ≥2 months of stable (≥2 weeks) treatment with glucocorticoids plus immunosuppressants and/or biologics; prednisone ≥7.5 mg/day or equivalent.
    3. Positive ANA, anti-dsDNA antibody, and/or anti-Smith antibody at screening.
    4. SLEDAI-2K >6 and clinical SLEDAI-2K ≥4 at screening. Patients with lupus nephritis (proteinuria >0.5 g/24h, UPCR >500 mg/g, or active urinary sediment) are exempt from clinical SLEDAI-2K requirement.
    5. Physician Global Assessment (PGA) ≥1.0 (0-3 VAS) at screening.
  3. For SSc Patients

    1. Diagnosis of SSc per 2013 ACR/EULAR criteria.
    2. Diffuse cutaneous SSc at screening.
    3. Active disease defined by at least one of: new SSc within 2 years; new/worsening skin or thoracic/abdominal involvement within 6 months; worsening skin thickening (mRSS ≥2); tendon friction rubs within 3 months; worsening respiratory symptoms with FVC decline ≥5% predicted or DLCO decline ≥10% predicted; or ILD progression on HRCT compared to 12 months prior.
    4. Refractory or relapsing disease after >6 months of conventional therapy including glucocorticoids, cyclophosphamide, immunosuppressants, and/or biologics.
  4. For AAV Patients

    1. Diagnosis of ANCA-associated vasculitis (MPA, GPA, EGPA) per 2022 ACR/EULAR criteria.
    2. Positive MPO-ANCA or PR3-ANCA.
    3. BVAS with at least 1 major item, 3 minor items, or 2 renal items.
    4. Failure of standard of care: no remission after ≥4 months of glucocorticoids plus cyclophosphamide/rituximab; relapse after prior remission; or persistent active disease despite ≥6 months of SOC.
  5. For IIM Patients

    1. Diagnosis of IIM (DM, ASS, IMNM) per 2017 ACR/EULAR criteria (probability ≥55%).
    2. Active disease defined by ≥2 abnormal core measures, or active myositis on muscle MRI, or active inflammation on muscle biopsy within 16 weeks.
    3. Positive myositis-specific autoantibodies.
    4. Refractory or relapsing disease after ≥6 months of conventional therapy including glucocorticoids, immunosuppressants, and/or biologics.
  6. For pSS Patients

    1. Diagnosis of primary Sjögren's syndrome per 2016 ACR/EULAR criteria.
    2. Positive anti-SSA/Ro antibody.
    3. ESSDAI ≥6 at screening.
    4. Refractory or relapsing disease after ≥6 months of conventional therapy including glucocorticoids, immunosuppressants, and/or biologics.

Exclusion Criteria:

  1. General Exclusion Criteria (All Patients):

    1. Coexisting autoimmune disease confounding disease activity/safety (stable ≥3 months may be eligible with approval).
    2. Anti-CD20 mAb/T-cell engager within 3 months; CD19/BCMA-targeted therapy within 6 months (exception with CD19⁺ B-cell > LLN and approval).
    3. Rapidly progressive glomerulonephritis (RPGN).
    4. NYHA III/IV heart failure; severe cardiac disease within 12 months.
    5. Severe CNS disease impairing compliance/assessments.
    6. Malignancy history (except cured non-melanoma skin cancer/carcinoma in situ, disease-free ≥3 years).
    7. Primary immunodeficiency.
    8. Uncontrolled infection (uncomplicated UTI/upper respiratory infection permitted).
    9. Positive HIV; positive HCV (except undetectable RNA); positive syphilis.
    10. Positive HBsAg; positive HBcAb (except undetectable HBV DNA).
    11. Positive EBV/CMV DNA/IgM at screening.
    12. Active/recurrent tuberculosis.
    13. Prior CAR-T or genetically modified immune cell therapy.
    14. Live attenuated vaccine within 4 weeks before enrollment.
    15. Hypersensitivity to cell therapy product components.
    16. Tacrolimus hypersensitivity or ≥Grade 3 toxicity requiring hospitalization.
    17. Other clinical trial participation within 30 days before screening.
    18. Pregnant/breastfeeding; childbearing potential unwilling to use effective contraception.
    19. Any other ineligible condition (investigator judgment).
  2. Exclusion Criteria for SLE

    1. Active/unstable neuropsychiatric SLE requiring intervention within 90 days.
    2. Anti-BAFF/APRIL therapy within required washout period; multiple NSAIDs within 14 days; inability to hold NSAIDs; intra-articular glucocorticoids within 6 weeks; immunosuppressants exceeding dose limits; hydroxychloroquine dose adjustment within 8 weeks; ACEI/ARB/SGLT2i adjustment within 4 weeks.
  3. Exclusion Criteria for AAV

    1. Alveolar hemorrhage requiring invasive ventilation beyond screening.
    2. Dialysis/plasmapheresis within 12 weeks.
    3. Renal transplantation history.
    4. Cyclophosphamide within 12 weeks; immunosuppressant discontinuation required 1 week before lymphodepletion.
    5. High-dose IV glucocorticoids within 4 weeks.
    6. Oral glucocorticoids >60mg prednisone equivalent daily for >6 weeks.
    7. Specific immunosuppressants/biologics within 4 weeks.
    8. Concomitant strong CYP3A4 inducers.
  4. Exclusion Criteria for IIM

    1. Severe rhabdomyolysis or CK ≥120×ULN at screening.
    2. FVC ≤50% predicted or DLCO ≤40% predicted at screening.
  5. Exclusion Criteria for SSc

    1. Significant respiratory disease other than ILD.
    2. FVC <50% or DLCO <40% predicted at screening/baseline.
    3. Lung transplantation listing/expected within 12 months.
    4. Scleroderma renal crisis within 6 months.
    5. Scleroderma-like disorders.
    6. Prior chlorambucil, bone marrow transplantation, or total lymphoid irradiation.
  6. Exclusion Criteria for pSS

    1. Active fibromyalgia interfering with assessment/requiring medication adjustment (stable permitted).
    2. Cyclophosphamide within 12 weeks; immunosuppressant discontinuation required 1 week before lymphodepletion.
    3. High-dose glucocorticoids (≥60mg/day) within 4 weeks.

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

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:RD06-05
CAR T-cell therapy administered intravenously after a lymphodepleting therapy regimen consisting of fludarabine and cyclophosphamide.

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
SLE (systemic lupus erythematosus)
時間枠:2 years
Proportion of patients achieving lupus low disease activity state (LLDAS) and DORIS(Definition Of Remission In SLE) remission, as well as the proportion of patients achieving drug-free remission
2 years
SLE (systemic lupus erythematosus)
時間枠:2 years
Proportion of SLE patients with renal involvement who achieved complete renal response (CRR) and partial renal response
2 years
SLE (systemic lupus erythematosus)
時間枠:2 years
Change in UPCR(Urine Protein/Creatinine Ratio) from baseline in SLE patients with renal involvement
2 years
SLE (systemic lupus erythematosus)
時間枠:2 years
Change in eGFR(estimated Glomerular Filtration Rate) from baseline in SLE patients with renal involvement
2 years
SLE (systemic lupus erythematosus)
時間枠:2 years
Changes in SLEDAI-2K, Physician Global Assessment (PGA), and British Isles Lupus Assessment Group (BILAG) score from baseline
2 years
SLE (systemic lupus erythematosus)
時間枠:2 years
Changes in anti-dsDNA antibody, C3 and C4 levels from baseline
2 years
AAV (ANCA-associated vasculitis)
時間枠:2 years
Change in Birmingham Vasculitis Activity Score (BVAS) from baseline. The Birmingham Vasculitis Activity Score (BVAS) ranges from a minimum of 0 to a maximum of 63, with higher scores indicating worse disease activity and clinical outcomes.
2 years
AAV (ANCA-associated vasculitis)
時間枠:2 years
Proportion of patients with vasculitis relapse (including major flare and minor flare)
2 years
IIM (idiopathic inflammatory myopathies)
時間枠:2 years
Major clinical remission assessed according to the 2016 ACR/EULAR myopathy remission criteria
2 years
SSc (systemic sclerosis)
時間枠:2 years
Changes in modified Rodnan Skin Score (mRSS) from baseline
2 years
SSc (systemic sclerosis)
時間枠:2 years
Changes in European Scleroderma Trials and Research group (EUSTAR) Activity Index from baseline
2 years
SSc (systemic sclerosis)
時間枠:2 years
Changes in Forced Vital Capacity (FVC) and Diffusing Capacity of the Lung for Carbon Monoxide (DLCO) from baseline in patients complicated with interstitial lung disease
2 years
SS (Sjögren's syndrome )
時間枠:2 years
Change in ESSDAI(EULAR Sjögren's Syndrome Disease Activity Index) score from baseline. ESSDAI has a score range from 0 to 105, with higher scores indicating greater disease activity and poorer clinical outcomes.
2 years
SS (Sjögren's syndrome )
時間枠:2 years
Change in ESPRI(EULAR Sjögren's Syndrome Patient Reported Index) score from baseline. ESSPRI ranges from a minimum of 0 to a maximum of 10, with higher scores indicating worse symptoms and poorer patient-reported outcomes.
2 years
SS (Sjögren's syndrome )
時間枠:2 years
Change in STAR(Sjögren's Tool for Assessing Response) score from baseline. STAR score ranges from 0 to 28, with higher scores indicating more severe disease status and poorer therapeutic response.
2 years

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

捜査官

  • 主任研究者:Qiong Fu, Doctor、Renji Hospital

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (推定)

2026年9月1日

一次修了 (推定)

2028年4月30日

研究の完了 (推定)

2029年4月30日

試験登録日

最初に提出

2026年4月7日

QC基準を満たした最初の提出物

2026年5月12日

最初の投稿 (実際)

2026年5月19日

学習記録の更新

投稿された最後の更新 (実際)

2026年7月16日

QC基準を満たした最後の更新が送信されました

2026年7月15日

最終確認日

2026年7月1日

詳しくは

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個々の参加者データ (IPD) を共有する予定はありますか?

いいえ

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いいえ

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