Using CD19 CAR T cells to treat refractory systemic lupus erythematosus

Open-Label, Non-Randomized, Single-Arm, Phase 1/2 Study of Anti-CD19 Chimeric Antigen Receptor T Cells for Refractory Systemic Lupus Erythematosus

This study is testing if a new type of immune cell therapy can help people with hard-to-treat systemic lupus erythematosus feel better.

Quick facts

• Phase: PHASE1; PHASE2
• Study type: Interventional
• Enrollment: 18 (estimated)
• Ages: 3 Years to 65 Years
• Sex: All
• Sponsor: Beijing GoBroad Hospital (other)
• Drugs / interventions: rituximab, belizumab, CAR T, methotrexate, cyclophosphamide
• Locations: 1 site (Beijing, Beijing Municipality)
• Trial ID: NCT06585514 on ClinicalTrials.gov

What this trial studies

This clinical trial evaluates the safety and efficacy of CD19 CAR T cell therapy in patients with refractory systemic lupus erythematosus (SLE). It is a single-center, open-label, non-randomized Phase I/II trial where participants will receive CD19 CAR T cells. The primary objectives include assessing the safety and tolerability of the treatment, determining the optimal biological dose, and evaluating the overall response rate in phase II. A total of 18 subjects will be enrolled to gather data on dose limiting toxicity and treatment efficacy.

Who should consider this trial

Good fit: Ideal candidates are individuals aged 3-65 with a diagnosis of refractory systemic lupus erythematosus or lupus nephritis.

Not a fit: Patients whose SLE is well-controlled with standard treatments may not benefit from this study.

Why it matters

Potential benefit: If successful, this treatment could provide a new therapeutic option for patients with refractory systemic lupus erythematosus.

How similar studies have performed: While CAR T cell therapy has shown promise in other conditions, this specific application for systemic lupus erythematosus is novel and has not been extensively tested.

Eligibility criteria

Inclusion Criteria:

1. Male or female, aged 3-65 years.
2. Have a diagnosis of SLE and meet the classification criteria of 2019 European League Against Rheumatism (EULAR) and the American College of Rheumatology (ACR).
3. Positive antinuclear antibody (ANA): ANA at a titer of ≥ 1:80 on Hep-2 cells or equivalent positive test (ever) and/or a positive anti-dsDNA serum antibody test (based on ELISA assay, ≥ 30 IU/mL).
4. Refractory SLE and/or refractory lupus nephritis (LN):

   • 4.1 Refractory SLE 4.1.1 Patients received at least 7.5 mg/kg/day of prednisolone to maintain low disease activity or the SLEDAI 2K score ≥8.

   4.1.2 Routine treatment is ineffective or the disease relapses after remission. Definition of routine treatment: use glucocorticoid (more than 1mg/kg/d) and cyclophosphamide for 6 months; and any of the following immunomodulatory drugs for more than 3 months: antimalarials, azathioprine, mycophenolate mofetil, methotrexate, leflunomide, tacrolimus, cyclosporine, and biological agents such as rituximab, belizumab, or telitacicept;

   • 4.2 Refractory LN 4.2.1 Diagnosis of SLE based on the 2019 European League Against Rheumatism (EULAR)/American College of Rheumatology (ACR), Biopsy-proven LN class III, IVa \[excluding III (C), IV-S (C) and IV-G (C)\] or, class V lupus nephritis combined with class III or IV, according to 2018 Revised International Society of Nephrology/Renal Pathology Society (ISN/RPS) criteria, see Appendix 3. Biopsy must be performed within 6 months before or during screening.

   4.2.2 Refractory lupus nephritis is defined as no induced remission to treatment regimens containing at least one immunosuppressant (including glucocorticoids, CTX, tacrolimus, MME, and cyclosporine) after 3 to 6 months, accompanied by no reduction (or worsening) of proteinuria or persistent antibody positives.
5. CD19+ on B cells and continuous withdrawal of the immunosuppressive drugs for more than 1 week.
6. The blood routine lymphocyte count of the subjects is \> 1 × 109/L, and there is no cell collection contraindication.
7. No severe allergy.
8. Eastern Cooperative Oncology Group (ECOG) performance status score 0 to 2.
9. Patients are expected to live for at least 90 days.
10. Subjects and/or their guardian must understand and sign the informed consent.

Exclusion Criteria:

An individual who meets any of the following criteria will be excluded from participation in this study:

1. Impaired consciousness or intracranial hypertension:

   * Intracranial pressure elevation was above 15 mmHg;
   * Organic encephalopathy syndrome, cerebrovascular accident, encephalitis or central nervous system vasculitis, visual impairment, and other brain lesions requiring intervention.
2. Symptomatic congestive heart failure or severe cardiac arrhythmia:

   * Previously documented left ventricular ejection fraction (LVEF) by echocardiography of \<45% in the 12 months;
   * Abnormal electrocardiogram (ECG): left bundle branch block, bifascicular block or any clinically meaningful ECG abnormality;
   * Congenital long QT syndrome or prolongation of the QT interval corrected for heart rate (QTcF) ≥ 470 ms. QTcF is calculated using Fridericia's Formula;
   * Any Class 3 or 4 cardiac disease as defined by the New York Heart Association Functional Classification;
   * Unstable or poorly controlled angina pectoris, including the prinzmetal variant of angina pectoris;
   * Myocardial infarction within 6 months.
3. Manifestations of severe respiratory system failure:

   * Hypoxemic respiratory failure: PaO2 \< 60 mmHg, PaCO2 \< 50 mmHg at sea level, resting and breathing air conditions;
   * Subjects with pulmonary hypertension (PH): mean pulmonary artery pressure (mPAP) ≥25 mmHg measured by right heart catheterization (RHC);
   * Subjects with hypercapnia (PaCO2 ≥ 50mmHg ) and/or ventilatory dysfunction (PH \<7.25 );
   * Oxygen inhalation was required to maintain oxygen saturation;
   * Acute or chronic respiratory diseases unrelated to SLE, such as acute pneumonia and interstitial lung disease.
4. Co-existence with other malignancies.
5. Disseminated intravascular coagulation (DIC).
6. Sepsis or other uncontrollable infections: active uncontrolled systemic bacterial, viral, fungal, or parasitic infection (except for fungal nail infection) or other clinically significant active disease process.
7. Uncontrollable diabetes: after at least 3 months of diet and exercise or similar treatment, fasting blood glucose (FBG) ≥ 8.0 mmol/L, postprandial blood glucose (PBG) ≥ 15 mmol/L, and glycosylated hemoglobin (HbA1c)≥8.0%; diabetic ketoacidosis or other uncontrollable complications of diabetes.
8. Serious mental illness: alcohol or drug abuse, dementia, or any other condition that would impair the subject's ability to receive the planned treatment or to understand informed consent at the study site.
9. Apparent and active intracranial lesions on cranial magnetic resonance imaging (MRI).
10. Underwent organ transplantation, excepting SCT.
11. Pregnant females or lactation.
12. Positive test for infectious hepatitis, acquired immune deficiency syndrome (AIDS) or syphilis.
13. No peripheral blood mononuclear cells (PBMC) collection or frozen PBMC for CAR T cell manufacturing.
14. eGFR CKD-EPI \< 30 ml/min/1.73m2.
15. Patients who are unable to discontinue immunosuppression agents for ≥7 days or whose condition recurs during discontinuation while the risk of serious adverse reactions is assessed by the investigator.
16. Any active skin disease that may interfere with the evaluation of SLE, including but not limited to psoriasis, dermatomyositis, systemic sclerosis, non-SLE skin manifestations (e.g., cutaneous vasculopathies, peripapillary dilatation, fingertip sclerosis, rheumatoid nodules, erythema multiforme, leg ulcers), or drug-induced lupus.

Where this trial is running

Beijing, Beijing Municipality

• Beijing GoBroad Hospital — Beijing, Beijing Municipality, China (RECRUITING)

Study contacts

• Study coordinator: Tengyu Wang

Conditions: Systemic Lupus Erythematosus, Lupus Nephritis, CD19 CAR-T