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IASO207 Injection for Active Refractory Systemic Lupus Erythematosus (SLE)

23. maj 2026 opdateret af: Xiangyu Zhao, Peking University People's Hospital

An Exploratory Clinical Study on the Treatment of Active Refractory Systemic Lupus Erythematosus With IASO207 Injection

This is a single-center, open-label, exploratory clinical study designed to evaluate the efficacy and safety of IASO207 Injection (in vivo CAR-T) in patients with active refractory systemic lupus erythematosus.

Studieoversigt

Status

Rekruttering

Intervention / Behandling

Detaljeret beskrivelse

This study is a single-arm, single-center, open-label, first-in-human (FIH) clinical trial designed to preliminarily evaluate the safety and efficacy of IASO207 injection, an in vivo chimeric antigen receptor T-cell (CAR-T) therapy, in patients with active, refractory systemic lupus erythematosus (SLE), and to determine the recommended dose for subsequent clinical development.

A standard "3+3" dose-escalation design will be employed during the dose-escalation phase, with three predefined dose levels: 5.0 × 10⁸ TU, 1.0 × 10⁹ TU, and 2.0 × 10⁹ TU. Each dose cohort will enroll 3-6 subjects, with a single administration of IASO207 injection.

The primary objective is to assess the safety and tolerability of IASO207 across different dose levels. Secondary and exploratory objectives include the characterization of pharmacokinetics, pharmacodynamics, and immunogenicity, as well as the preliminary evaluation of clinical efficacy in patients with active refractory SLE. The results of this study are expected to inform dose selection and support subsequent clinical trials.

Undersøgelsestype

Interventionel

Tilmelding (Anslået)

18

Fase

  • Tidlig fase 1

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiekontakt

Undersøgelse Kontakt Backup

Studiesteder

      • Beijing, Kina, 100044
        • Rekruttering
        • Peking University People's Hospital
        • Underforsker:
          • Meng Lv, M.D, Ph.D
        • Kontakt:
        • Kontakt:
        • Ledende efterforsker:
          • Xiangyu Zhao, M.D, Ph.D
        • Ledende efterforsker:
          • Jing He, M.D, Ph.D

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

  • Voksen
  • Ældre voksen

Tager imod sunde frivillige

Ingen

Beskrivelse

Inclusion Criteria:

  1. Subjects aged 18-75 years old, regardless of gender.
  2. Subjects diagnosed with active refractory SLE: a) Confirmed by the 2019 European League Against Rheumatism (EULAR)/American College of Rheumatology (ACR) classification criteria or the 2012 Systemic Lupus Erythematosus Collaborative Clinic (SLICC) criteria for at least 24 weeks; b) SLE Disease Activity Index 2000 (SLEDAI-2K) score ≥ 8, with at least 1 organ system having a BILAG-2004 A-class activity score at screening, or 2 organ systems having a BILAG-2004 B-class activity score; c) Previously treated with standardized glucocorticoids and at least two immunosuppressants/adjusters, antimalarial drugs or biologics for at least 3 months.
  3. Positive for disease-related pathogenic antibodies: Anti-nuclear antibody (ANA) positive and/or anti-dsDNA positive and/or anti-Smith positive.
  4. Allowed to use ≤ 20mg/d prednisone or equivalent dose of corticosteroids at screening, and use at a stable dose for at least 2 weeks. Note: Local or inhaled corticosteroids (or its immunomodulators) can be used concurrently;
  5. If antimalarial treatment has been initiated for ≥ 12 weeks before screening and is used at a stable dose for at least 8 weeks, it is allowed to continue in the study (maximum hydroxychloroquine dose ≤ 400mg/d).
  6. If immunosuppressants have been used before screening, they must be used at a stable dose for at least 4 weeks.
  7. Laboratory tests must meet the following conditions: a) Blood routine: Absolute neutrophil count (ANC) ≥ 1.0×10^9/L; Absolute lymphocyte count (ALC) ≥ 0.3×10^9/L; Hemoglobin ≥ 60 g/L; Platelets ≥ 50×10^9/L b) Liver function: Alanine aminotransferase (ALT) and aspartate aminotransferase (AST) ≤ 2.5× upper limit of normal (ULN); Serum total bilirubin ≤ 1.5×ULN (Gilbert's syndrome ≤ 3.0×ULN).
  8. The subject and their spouse agree to take effective contraceptive measures (excluding safe period contraception) from the time of signing the informed consent form by the subject until one year after IASO207 injection treatment.
  9. The subject must agree to sign or personally write and present the signed informed consent form approved by the ethics committee before starting any screening procedure.

Exclusion Criteria:

Disease-related:

  1. Diagnosed with drug-induced SLE.
  2. Complicated with other autoimmune diseases that may affect the assessment of the study, including but not limited to Sjögren's syndrome, psoriasis, rheumatoid arthritis.
  3. Had a catastrophic antiphospholipid syndrome or developed a severe antiphospholipid syndrome within 1 year before screening.
  4. The study disease involved neurological symptoms with a BILAG-2004 activity score of class A.

    Other medical history-related:

  5. Known primary immunodeficiency (congenital or acquired).
  6. The subject has uncontrollable active fungal, viral, bacterial or other infections (existing persistent infection-related signs/symptoms, not improved after appropriate anti-infection treatment) or requires intravenous anti-infection drug treatment for infection.
  7. Positive hepatitis B surface antigen (HBsAg), or positive hepatitis B core antibody (HBcAb) and abnormal peripheral blood hepatitis B virus (HBV) DNA detection (defined as HBV DNA quantification above the normal reference range of the testing center or positive HBV DNA qualitative detection); positive hepatitis C virus (HCV) antibody and positive peripheral blood hepatitis C virus (HCV) RNA; positive Human Immunodeficiency Virus (HIV) antibody; positive cytomegalovirus (CMV) DNA detection; positive Treponema pallidum specific antibody and positive rapid plasma reagin test for syphilis.
  8. Severe heart disease: including but not limited to unstable angina pectoris and/or myocardial infarction within 12 months of screening, any congestive heart failure (NYHA classification ≥ III), and a history of severe arrhythmia; or left ventricular ejection fraction (LVEF) < 45%.
  9. Severe asthma or chronic obstructive pulmonary disease (COPD), with stable treatment considered for mild or moderate asthma or COPD by the investigator and sponsor; or resting arterial blood oxygen saturation < 91%.
  10. Evaluated by the investigator as having a severe bleeding risk.
  11. Evaluated by the investigator as having severe liver dysfunction.
  12. History of severe kidney disease; or eGFR < 30 mL/min/1.73m2 calculated by the Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI) formula.
  13. Acute cerebrovascular disease events occurred within 6 months before enrollment, including transient ischemic attack or stroke history.
  14. Any severe and/or uncontrolled comorbid diseases as assessed by the investigator.
  15. Had a malignant tumor within 5 years before screening, excluding cured cervical carcinoma in situ, basal cell or squamous cell skin cancer, locally advanced prostate cancer after radical surgery, breast duct carcinoma in situ after radical surgery, or papillary thyroid carcinoma after radical surgery.
  16. Had a clear history of mental disorder or a history of substance abuse for mental disorders that cannot be quit.
  17. Known allergy to the components of IASO207 injection or to the supportive drugs required for the toxicity management of CAR-T cell therapy (such as tocilizumab).

    Previous and concurrent treatments:

  18. History of organ transplantation.
  19. History of autologous or allogeneic stem cell transplantation.
  20. History of cell therapy or CD19-targeted drug treatment.
  21. Received targeted CD20 biologic therapy within 12 weeks before screening, such as rituximab, obinutuzumab.
  22. Received plasma exchange or immunoadsorption treatment within 12 weeks before screening.
  23. Had or planned to have major surgery or surgical treatment caused by any reason within 12 weeks before screening.
  24. Have participated in the treatment of other investigational drugs (except for placebo) within the previous 4 weeks or 5 half-lives (whichever is longer);
  25. Have received a BAFF antagonist, such as belimumab or tixagevimab, within the previous 4 weeks;
  26. Have received live attenuated vaccine within the previous 4 weeks;
  27. Pregnant or lactating women;
  28. Other situations deemed unsuitable for inclusion by the investigators.

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Behandling
  • Tildeling: N/A
  • Interventionel model: Enkelt gruppeopgave
  • Maskning: Ingen (Åben etiket)

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Eksperimentel: IASO207 Injection
IASO207 Injection will be infused at 5.0×10^8 TU or 1.0×10^9 TU or 2.0×10^9 TU after enrollment
IASO207 is a third-generation replication-deficient self-inactivating lentiviral vector that carries the gene encoding a second-generation anti-human CD19 chimeric antigen receptor (CD19 CAR) containing the 4-1BB co-stimulatory factor. IASO207 has been engineered through surface modification of the lentiviral envelope to enable it to selectively bind and transduce T cells within the body, thereby directly generating CD19 CAR-T cells in vivo.

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Safety endpoint - Adverse Events (AEs)
Tidsramme: up to 2 years from IASO207 Injection infusion
Incidence and severity of adverse events as assessed by NCI-CTCAE v5.0 (except CRS and ICANS assessed according to the criteria of 2019 ASTCT criteria).
up to 2 years from IASO207 Injection infusion
Safety endpoint - The incidence of dose-limiting toxicity (DLT)
Tidsramme: 28 days from IASO207 Injection infusion
Percentage of participants who experienced DLT within 28 days after IASO207 administration
28 days from IASO207 Injection infusion

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Pharmacokinetic Endpoint - Cmax (viral particle)
Tidsramme: Up to 7 days from IASO207 Injection infusion
Maximum concentration (Cmax) of viral particle titer in peripheral blood will be observed and calculated.
Up to 7 days from IASO207 Injection infusion
Pharmacokinetic Endpoint - Cmax (VCN)
Tidsramme: up to 2 years from IASO207 Injection infusion
The maximum concentration (Cmax) of lentiviral vector copy number (VCN) in peripheral blood after infusion.
up to 2 years from IASO207 Injection infusion
Pharmacodynamic Endpoint - Ferritin
Tidsramme: up to 2 years from IASO207 Injection infusion
Changes in the levels of Ferritin.
up to 2 years from IASO207 Injection infusion
Pharmacodynamic Endpoint - IL-6
Tidsramme: up to 2 years from IASO207 Injection infusion
Changes in the levels of IL-6.
up to 2 years from IASO207 Injection infusion
Efficacy endpoint - Response rate of SRI-4 after infusion
Tidsramme: up to 2 years from IASO207 Injection infusion
SLE Responder Index (SRI)-4 is defined as follows with all criteria compared with Baseline: 1. ≥ 4-point reduction in Systemic Lupus Erythematosus Disease Activity Index 2000 (SLEDAI-2K) score. 2. No worsening of the overall condition (< 0.3 point increase in Physician's Global Assessment [PhGA]). 3. No new British Isles Lupus Assessment Group (BILAG) A or more than 1 new BILAG B disease activity scores.
up to 2 years from IASO207 Injection infusion
Efficacy endpoint - lupus low disease activity state (LLDAS) rate through 2 years after infusion
Tidsramme: up to 2 years from IASO207 Injection infusion
Proportions of subjects achieving LLDAS at each time point
up to 2 years from IASO207 Injection infusion
Efficacy endpoint - Definitions of Remission in SLE (DORIS) rate through 2 years after infusion
Tidsramme: up to 2 years from IASO207 Injection infusion
Proportions of subjects achieving remission according to the DORIS as assessed by SLEDAI-2K Scale, PhGA score and concomitant medication use
up to 2 years from IASO207 Injection infusion
Efficacy endpoint - The changes in SLEDAI-2K scores
Tidsramme: up to 2 years from IASO207 Injection infusion
At each visit site, the patients were scored using the SLEDAI-2K, and then the changes in scores compared between each visit point and the baseline score were evaluated
up to 2 years from IASO207 Injection infusion
Efficacy endpoint - The changes in PGA scores
Tidsramme: up to 2 years from IASO207 Injection infusion
At each visit site, the patients were scored using the PGA, and then the changes in scores compared between each visit point and the baseline score were evaluated
up to 2 years from IASO207 Injection infusion
7. Pharmacokinetic Endpoint - Tmax (viral particle)
Tidsramme: Up to 7 days from IASO207 Injection infusion
Peak time (Tmax) of viral particle titer in peripheral blood will be observed and analyzed.
Up to 7 days from IASO207 Injection infusion
Pharmacokinetic Endpoint - AUC0-7 (viral particle)
Tidsramme: Up to 7 days from IASO207 Injection infusion
AUC0-7d refers to the area under the concentration-time curve from day 0 to day 7
Up to 7 days from IASO207 Injection infusion
Pharmacokinetic Endpoint - Cmax (CAR-T cells)
Tidsramme: up to 2 years from IASO207 Injection infusion
The maximum concentration (Cmax) of CAR-T cells in peripheral blood after infusion
up to 2 years from IASO207 Injection infusion
Pharmacokinetic Endpoint - Tmax (CAR-T cells)
Tidsramme: up to 2 years from IASO207 Injection infusion
The time for CAR-T cells to reach the maximum concentration (Tmax) after infusion
up to 2 years from IASO207 Injection infusion
Pharmacokinetic Endpoint - AUC (CAR-T cells)
Tidsramme: up to 2 years from IASO207 Injection infusion
Area under the curve of 28 days, 90 days, 180 days, and the last time point of PK measurement (AUC0-28d, AUC0-90d, AUC0-180d, AUC0-last) for CAR-T cells.
up to 2 years from IASO207 Injection infusion
Pharmacokinetic Endpoint - Tmax (VCN)
Tidsramme: up to 2 years from IASO207 Injection infusion
The time for VCN to reach the maximum concentration (Tmax) after infusion
up to 2 years from IASO207 Injection infusion
Pharmacokinetic Endpoint - AUC (VCN)
Tidsramme: up to 2 years from IASO207 Injection infusion
Area under the curve of 28 days, 90 days, 180 days, and the last time point (AUC0-28d, AUC0-90d, AUC0-180d, AUC0-last) for VCN
up to 2 years from IASO207 Injection infusion
Pharmacodynamic Endpoint - Pathogenic antibodies
Tidsramme: up to 2 years from IASO207 Injection infusion
Changes in serum levels of pathogenic antibodies such as ANA, anti-dsDNA, and anti-Smith.
up to 2 years from IASO207 Injection infusion
Pharmacodynamic Endpoint - Complement levels
Tidsramme: up to 2 years from IASO207 Injection infusion
Changes in measures of C3, C4.
up to 2 years from IASO207 Injection infusion
Pharmacodynamic Endpoint - Immune cell subsets
Tidsramme: up to 2 years from IASO207 Injection infusion
Changes in the levels of Immune cell subsets
up to 2 years from IASO207 Injection infusion
Pharmacodynamic Endpoint - Serum immunoglobulin
Tidsramme: up to 2 years from IASO207 Injection infusion
Changes in serum immunoglobulin (IgG, IgA, IgM) levels from baseline.
up to 2 years from IASO207 Injection infusion
Pharmacodynamic Endpoint - CRP
Tidsramme: up to 2 years from IASO207 Injection infusion
Changes in the levels of CRP
up to 2 years from IASO207 Injection infusion

Andre resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Immunogenicity
Tidsramme: up to 2 years from IASO207 Injection infusion
Prevalence and titer of confirmed human anti-CAR antibodies in peripheral blood.
up to 2 years from IASO207 Injection infusion
Replication competent lentivirus (RCL)
Tidsramme: up to 2 years from IASO207 Injection infusion
Prevalence of replication-competent lentivirus (RCL) in peripheral blood.
up to 2 years from IASO207 Injection infusion
Virus shedding
Tidsramme: Up to 7 days from IASO207 Injection infusion
Presence of viral shedding in body fluid samples (urine, feces, and saliva)
Up to 7 days from IASO207 Injection infusion

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Efterforskere

  • Ledende efterforsker: XiangYu Zhao, M.D, Ph.D, Peking University People's Hospital
  • Ledende efterforsker: Jing He, M.D, Ph.D, Peking University People's Hospital

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart (Anslået)

25. maj 2026

Primær færdiggørelse (Anslået)

30. maj 2029

Studieafslutning (Anslået)

30. maj 2030

Datoer for studieregistrering

Først indsendt

1. maj 2026

Først indsendt, der opfyldte QC-kriterier

23. maj 2026

Først opslået (Faktiske)

1. juni 2026

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

1. juni 2026

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

23. maj 2026

Sidst verificeret

1. maj 2026

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Kliniske forsøg med IASO207 Injection

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