Tests MB-CART19.1 cell therapy in adults with hard-to-treat lupus

Trial details

Who runs it

Miltenyi Biomedicine GmbH

Trial code

NCT06189157

Record updated

26 November 2025

Original description

This is a phase l/ll open-label, multicentre, interventional single-arm trial of MB-CART19.1 in patients with refractory SLE systemic lupus erythematosus. In the phase I part, a maximum of n=12 patients will be treated in a maximum of 3 dose levels.Read full original descriptionShow less

An Open-label Phase I/IIa, Multicentre, Interventional Single-arm Trial of MB-CART19.1 in Patients With Refractory SLE

This is a phase l/ll open-label, multicentre, interventional single-arm trial of MB-CART19.1 in patients with refractory SLE systemic lupus erythematosus. In the phase I part, a maximum of n=12 patients will be treated in a maximum of 3 dose levels.

In the phase IIa part, a maximum of n=17 will be treated (n=10 patients in a 1st stage + n=7 patients in a 2nd stage). This includes the patients from the phase I part treated on the recommended dose level.

Inclusion: Patients at least 18 years of age; Signed and dated informed consent before the conduct of any trial-specific procedure; SLE fulfilling the 2019 ACR/EULAR classification criteria (refer to Appendix 8); One BILAG A or two BILAG B despite treatment with at least two of the following treatment options: MMF, cyclophosphamide, rituximab belimumab, anifrolumab, methotrexate, azathioprine; SLE with major organ involvement defined as either:; Presence of active lupus nephritis according to the following criteria:; Histology proven class III or IV lupus nephritis according to ISN/RPS 2003 classification; Urine protein-to-creatinine ratio (UPCR) >1 in 24-hour urine collection; Glomerular filtration rate (eGFR) of ≥30 mL/min/1.73 m2; No history of kidney transplantation; Lupus with heart involvement (e.g., myocarditis, pericarditis, endocarditis) as measured by MRI or echocardiography/ultrasound; Lupus with pulmonary involvement (Lupus pleuritis, pulmonary arterial hypertension (PAH)) or lung disease defined as:; Forced Vital Capacity (FVC) ≥ 60 % OR; Forced Expiratory Volume (FEV1) ≥ 60 %,Total Lung Capacity (TLC) ≥ 60 %, DLCO (diffusion capacity) ≥ 60 % (according to ATS/ERS guidelines); Absolute CD3+ T cell count ≥ 100/µl; No childbearing potential or negative pregnancy test at screening and before chemotherapy in women with childbearing potential. Subjects must agree to use a contraceptive method from screening until 12 months after the administration of the IMP; Fully vaccinated against SARS-CoV-2 according to the recommendations of RKI or confirmed SARS-CoV-2 infection within the last 6 months.

Exclusion: Medications:; Systemic corticosteroids >10 mg within 7 days prior to leukapheresis; T cell targeting drugs (e.g., mycophenolate mofetil, calcineurin inhibitors) within 21 days prior to leukapheresis; Prior treatment with anti-CD19 therapy; Previous adoptive T cell therapy or any gene therapy including CAR T cell therapy; Live vaccines within 30 days prior to leukapheresis; Current cytotoxic drugs; Women of childbearing potential (WOCBP) who do not agree to use highly effective contraceptive measures (Pearl index < 1) or practice true sexual abstinence from any heterosexual intercourse (true abstinence is only acceptable if it is in line with the preferred and usual life style of the participant) or have a vasectomised partner as the sole sexual partner (the vasectomised partner must have received medical assessment of the surgical success) for at least 1 month before the study start, during the study and in the 12 months following the last dose of study treatment; A woman is considered a WOCBP, i.e. fertile, following menarche and until becoming post-menopausal unless permanently sterile. WOCBP who want to become pregnant after completing treatment should seek advice about oocyte cryoconservation prior to treatment because of possible irreversible infertility. WOCBP must refrain from egg donation throughout the study until 12 months after the last dose of study treatment; Highly effective methods of contraception include hormonal contraceptives associated with inhibition of ovulation (oral, intravaginal, transdermal, injectable, implantable) and intrauterine devices or systems (e.g. hormonal and non-hormonal) and bilateral tubal occlusion; Permanent sterilization methods include hysterectomy, bilateral salpingectomy and bilateral oophorectomy; A post-menopausal state is defined as no menses for 12 months without an alternative medical cause; Men with non-pregnant WOCBP partners who do not agree to use highly effective contraceptive measures (Pearl index < 1, e.g. spermicide and condom or other highly effective contraceptive measures (Pearl index < 1) taken by their WOCBP partner) or practice true sexual abstinence from any heterosexual intercourse (true abstinence is only acceptable if it is in line with the preferred and usual life style of the participant.), unless they are surgically sterile (meaning at least 2 consecutive analyses following vasectomy demonstrate absence of sperms in the ejaculate), during the study and in the 12 months following the last dose of study treatment; Men should seek advice about sperm conservation prior to treatment because of possible irreversible infertility. Men must furthermore refrain from sperm donation throughout the study until 12 months after the last administration of study treatment; Concurrent participation in any other interventional trial; Active clinically significant central nervous system (CNS) dysfunction (including but not limited to uncontrolled seizure disorders, cerebrovascular ischemia or hemorrhage, dementia, paralysis); Uncontrolled diabetes mellitus; Therapy induced lung disease and tuberculosis; Liver function: Severe hepatic insufficiency defined as a Child-Pugh score > 10(C) (Appendix 10); Known history of infection with human immunodeficiency virus or active infection with hepatitis B (hepatitis B surface antigen positive); Known history of infection with hepatitis C virus unless treated and confirmed to be polymerase chain reaction (PCR) negative; Any active, uncontrolled bacterial, viral or fungal infection including SARS-CoV-2; History of hematopoietic stem cell or solid organ transplantation; Hypersensitivity against any drug or its ingredients/impurities that is scheduled or likely to be given during trial participation, e.g., as part of the mandatory preparative chemotherapy or rescue medication/salvage therapies for treatment related toxicities; Cardiac function: Unstable coronary heart disease; left ventricular ejection fraction (LVEF) < 50 %; no active myocarditis; Renal function: eGFR < 30 ml/min/1.73 m2; History of a malignancy unless disease free for ≥ 5 years with the exception of basal or squamous cell skin cancer; Forced Vital Capacity (FVC) < 60 %, FEV1 < 60 %, Total Lung Capacity (TLC) < 60 % and DLCO (diffusion capacity) < 60 %; BILAG A or BILAG B for neuropsychiatric SLE; Irreversible organ damage; Contraindication of trial related procedures as judged by the investigator; Inability to understand the procedures and risks associated with the trial.

ClinicalTrials.gov NCT06189157