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

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.

Study Overview

• Status: Recruiting
• Conditions: Dermatomyositis; Dermatomyositis, Juvenile
• Intervention / Treatment: Drug: Anti-CD19 UCAR-T cells

Detailed Description

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 will be terminated.Each dose group is expected to enroll 3 to 6 patients, with a total of 9 to 18 patients anticipated in the trial.

• Study Type: Interventional
• Enrollment (Estimated): 18
• Phase: Phase 1

Contacts and Locations

• Study Contact: Name: Lu Mei ping, M.D; Phone Number: +86 13685773988; Email: meipinglu@zju.edu.cn

Study Locations

• China
  • Zhejiang
    • Hangzhou, Zhejiang, China
      • Recruiting
      • Children's Hospital Zhejiang University School of Medicine, Hangzhou, zhejiang
      • Contact: Meiping Lu, M.D; Phone Number: +86 13685773988; Email: meipinglu@zju.edu.cn

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: Child; Adult; Older Adult
• Accepts Healthy Volunteers: No

Description

Inclusion Criteria:

• (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.

Exclusion Criteria:

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.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: N/A
• Interventional Model: Single Group Assignment
• Masking: None (Open Label)

Number of Arms

1

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: Anti-CD19 UCAR-T cells	Drug: Anti-CD19 UCAR-T cells; A single infusion of CD19 UCAR-T cells will be administered intravenously after lymphodepletion chemotherapy.

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
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

Secondary Outcome Measures

Outcome Measure	Time Frame
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

Other Outcome Measures

Outcome Measure	Time Frame
Duration of disease remission (DOR) after anti-CD19 UCAR-T cells infusion [Long-term Efficacy]	2 years
Time to B cell recovery after anti-CD19 UCAR-T cells infusion.	1 years

Collaborators and Investigators

• Sponsor: Chongqing Precision Biotech Co., Ltd

Study record dates

Study Major Dates

• Study Start (Estimated): November 11, 2024
• Primary Completion (Estimated): November 10, 2026
• Study Completion (Estimated): November 10, 2027

Study Registration Dates

• First Submitted: November 11, 2024
• First Submitted That Met QC Criteria: November 11, 2024
• First Posted (Estimated): November 13, 2024

Study Record Updates

• Last Update Posted (Estimated): November 13, 2024
• Last Update Submitted That Met QC Criteria: November 11, 2024
• Last Verified: November 1, 2024

More Information

Terms related to this study

• Keywords: Dermatomyositis; CD19; Universal CAR-T; UCAR-T
• Additional Relevant MeSH Terms: Musculoskeletal Diseases; Nervous System Diseases; Muscular Diseases; Neuromuscular Diseases; Connective Tissue Diseases; Skin Diseases; Myositis; Polymyositis; Dermatomyositis
• Other Study ID Numbers: PBC081

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No
• product manufactured in and exported from the U.S.: No