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El ensayo clínico NCT06686524 para Dermatomyositis, Juvenile, Dermatomiositis está reclutando. Consulte la vista de tarjeta del Radar de Ensayos Clínicos y las herramientas de descubrimiento de IA para conocer todos los detalles. O haga cualquier pregunta aquí.
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Clinical Study of CD19 Targeted Universal Chimeric Antigen Receptor T Lymphocytes (UCAR-T) for the Treatment of Refractory Juvenile Dermatomyositis (RJDM) Fase I 18 Terapia celular Etiqueta abierta

Reclutando
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El ensayo clínico NCT06686524 está diseñado para estudiar el tratamiento de Dermatomyositis, Juvenile, Dermatomiositis. Es un estudio intervencionista de Fase I. Su estado actual es: reclutando. El estudio se inició el 11 de noviembre de 2024, con el objetivo de reclutar a 18 participantes. Dirigido por Chongqing Precision Biotech Co., Ltd, se espera que finalice el 10 de noviembre de 2027. Los datos se actualizaron por última vez en ClinicalTrials.gov el 13 de noviembre de 2024.
Resumen
This study is an open-label, single-arm, dose-escalation trial primarily designed to evaluate the safety and efficacy of a universal CAR-T cell therapy targeting CD19 in the treatment of patients with RJDM. Additionally, the study aims to characterize its pharmacokinetic and pharmacodynamic properties, explore its role in immune system reconstitution, and assess long-term survival benefits.
Descripción detallada
This study adopts the "3+3" design, with a total of three dosage groups (1 × 107/kg, 3 × 107/kg, 6 × 107/kg). The study will start from the low dose group. Only when the present dose group has completed enrollment and no DLT has been observed, the study could escalate to the next dose group based on the evaluation of efficacy and cell kinetic data. If no DLT is observed even in the highest dose group, the escalation ...Mostrar más
Título oficial

Clinical Study of CD19 Targeted Universal Chimeric Antigen Receptor T Lymphocytes (UCAR-T) for the Treatment of Refractory Juvenile Dermatomyositis (RJDM)

Condiciones médicas
Dermatomyositis, JuvenileDermatomiositis
Otros ID del estudio
  • PBC081
Número del NCT
NCT06686524
Inicio del estudio (real)
2024-11-11
Última actualización
2024-11-13
Fecha de finalización (estimada)
2027-11-10
Inscripción (prevista)
18
Tipo de estudio
Intervencionista
FASE
Fase I
Estado general
Reclutando
Palabras clave
Dermatomyositis
CD19
UCAR-T
Universal CAR-T
Objetivo principal
Tratamiento
Método de asignación
N/A
Modelo de intervención
Grupo único
Enmascaramiento
Ninguno (Abierto)
Brazos / Intervenciones
Grupo de participantesIntervención/Tratamiento
ExperimentalAnti-CD19 UCAR-T cells
Anti-CD19 UCAR-T cells
A single infusion of CD19 UCAR-T cells will be administered intravenously after lymphodepletion chemotherapy.
Resultado primario
Medida de resultadoDescripción de la medidaPeriodo de tiempo
Incidence of Treatment-Emergent Adverse Events [Safety and Tolerability]
The incidence of adverse events after CAR-T cell infusion was assessed by CTCAE, version 5.0.
28 dyas
Total improvement score (TIS) after anti-CD19 UCAR-T cells infusion.
The total improvement score between 0-100 also corresponds to the degree of improvement, with higher improvement scores indicating greater improvement.
6 months
Disease Activity Score (DAS) after anti-CD19 UCAR-T cells infusion.
Including musculoskeletal system score and skin mucosal score, with a total score of 20 points. The higher the score, the higher the disease activity
6 months
Changes of myositis specific antibody levels and serum muscle enzyme levels after anti-CD19 UCAR-T cells infusion.
6 months
Improvement in muscle inflammation infiltration by MRI after anti-CD19 UCAR-T cells infusion.
6 months
Childhood Myositis Assessment Scale (CMAS) score after anti-CD19 UCAR-T cells
The total score is 52 points, the lower the score, the weaker the muscle strength and the more severe the disease.
6 months
Resultado secundario
Medida de resultadoDescripción de la medidaPeriodo de tiempo
Cmax of anti-CD19 UCAR-T cells [Cell dynamics]
1 month
Tmax of anti-CD19 UCAR-T cells [Cell dynamics]
1 month
AUCs of anti-CD19 UCAR-T cells [Cell dynamics]
1 month
Changes of myth enzyme after anti-CD19 UCAR-T cells
1 year
Asistente de participación
Criterios de elegibilidad

Criterios de edad
Niño, Adulto, Adulto mayor
Edad mínima
5 Years
Criterios de sexo
Todos

  • (1) Age ≥ 5 years old;

  • (2) Diagnosis of juvenile dermatomyositis (JDM) according to Bohan and Peter criteria;

  • (3) Meeting the classification criteria for RJDM, and meeting condition ① and any one of ② to ⑤ conditions:

    • Intolerance or inadequate response to glucocorticoids (prednisone 1-2mg/kg/d or equivalent dose of other hormones) and at least two immunosuppressants, with hormone therapy lasting for at least 6 months;

      • Rapid progression of the disease and/or involvement of organs such as lungs, heart, and gastrointestinal tract;

        • Calcification of subcutaneous or muscular and articular tissues;

          • Repeated skin rashes or ulcers;

            • Repeated or persistent muscle weakness (muscle magnetic resonance imaging indicating widespread, diffuse edema or a Children's Myositis Assessment Scale (CMAS) score < 48, and at least two abnormal results among the following five core measurement indicators: Physician's Global Assessment (PhGA) ≥ 2cm, Patient's Global Assessment (PtGA) ≥ 2cm, Disease Activity Score (DAS) ≥ 2 points, Child Health Assessment Questionnaire (C-HAQ) total score ≥ 0.25 points, and muscle enzyme level > 1.5 times the upper limit of normal (ULN));

  • (4)Patients with immune-mediated necrotizing myopathy who are positive for SRP or HMGCR antibodies meet the criteria for RJDM and can be directly included;

  • (5) Basic normal function of important organs:

    • Cardiac function: Left ventricular ejection fraction (LVEF) ≥55%, with no significant abnormalities observed in the electrocardiogram;

      • Renal function: eGFR ≥ 30mL/min/1.73m2;

        • Liver function: AST and ALT ≤3.0 ULN, total bilirubin ≤2.0×ULN (excluding those caused by primary diseases);

          • Pulmonary function: SpO2 ≥92%;

  • (6) Female subjects of childbearing age have a negative result in the urine pregnancy test and agree to take effective contraceptive measures during the trial until one year after infusion;

  • (7) The patient or their guardian agrees to participate in this clinical trial and signs an informed consent form, indicating their understanding of the purpose and procedures of the clinical trial and their willingness to participate in the study.

Subjects meeting any of the following criteria will be excluded from this trial:

  • (1) Previously received CAR-T cell therapy (except for those whose safety risks have been judged as eliminated by the investigator);
  • (2) Accompanied by primary immunodeficiency disease or severe secondary immunodeficiency disease that has not been corrected;
  • (3) Accompanied by severe, active, or uncontrolled infectious diseases, including but not limited to active tuberculosis, latent tuberculous infection, active viral hepatitis, etc.;
  • (4) Known to have active malignant diseases or confirmed malignancies before screening (including hematological malignancies and solid tumors, except for resected and cured cutaneous basal cell carcinoma);
  • (5) Suffering from congenital heart disease or having a history of acute myocardial infarction within 6 months, or severe arrhythmia (including multifocal frequent ventricular supraventricular tachycardia, ventricular tachycardia, etc.); or complicated with moderate to large pericardial effusion, severe myocarditis, etc.; or unstable vital signs requiring vasopressors to maintain blood pressure;
  • (6) Accompanied by other diseases that require long-term use of glucocorticoids or immunosuppressants;
  • (7) Received solid organ transplantation or hematopoietic stem cell transplantation within 3 months before screening; or presence of acute graft-versus-host disease (GVHD) of grade 2 or above within 2 weeks before screening;
  • (8) Positive for hepatitis B surface antigen (HBsAg) or hepatitis B core antibody (HBcAb) and peripheral blood hepatitis B virus (HBV) DNA titer detection is greater than the normal reference range; or positive for hepatitis C virus (HCV) antibody and peripheral blood hepatitis C virus (HCV) RNA titer detection is greater than the normal reference range; or positive for human immunodeficiency virus (HIV) antibody; or positive for syphilis test;
  • (9) Received live vaccines within 4 weeks before screening;
  • (10) Positive blood pregnancy test;
  • (11) Participated in other clinical trials within 3 months before enrollment;
  • (12) Other conditions that the investigator considers unsuitable for participation in the study.
Chongqing Precision Biotech Co., Ltd logoChongqing Precision Biotech Co., Ltd
Contactos centrales del estudio
Contacto: Lu Mei ping, M.D, +86 13685773988, [email protected]
1 Centros del estudio en 1 países

Zhejiang

Children's Hospital Zhejiang University School of Medicine, Hangzhou, zhejiang, Hangzhou, Zhejiang, China
Meiping Lu, M.D, Contacto, +86 13685773988, [email protected]
Reclutando