Phase 1 Study of HBI0101 CAR-T in Refractory B-Cell Autoimmune Diseases

Polina Stepensky

Status and phase

Enrolling

Phase 1

Conditions

Rheumatoid Arthritis (RA)

Systemic Sclerosis (SSc)

Idiopathic Inflammatory Myopathy (IIM)

Systemic Lupus Erythematosus (SLE)

Treatments

Biological: HBI0101 CART

Study type

Interventional

Funder types

Other

Identifiers

NCT07085676

HBI0101 ARD 001

Details and patient eligibility

About

A Phase 1 study of HBI0101 BCMA-CART in B-Cell Mediated Autoimmune Rheumatic Diseases. The goal of the study is evaluation of safety and identification of the maximum HBI0101 CART dose that may be administered safely to patients with B-cell mediated autoimmune disease.

Full description

Up to 60 subjects with B-cell mediated autoimmune rheumatic diseases will be enrolled in a single-arm, open-label, single-site Phase 1 study.

The study includes 2 parts. The first Part A is an establishment of the safety profile followed by a dose ranging, maximum tolerated dose (MTD) study and the second Part B is an extension phase to further evaluate safety at the selected safe dose.

Eligible subjects will undergo leukapheresis procedure to provide starting material for manufacturing of HBI0101 CART investigational product. Each eligible subject will receive a single dose of HBI0101 CART cells. Prior to administration of HBI0101 CART, the study subjects will undergo lymphodepletion. Following administration of HBI0101 CART the subjects will be hospitalized for several days and then will return for routine follow-up periodical visits until 48 months after infusion.

Enrollment

60 estimated patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Age: 18~65 years old
Diagnosis of B-cell mediated autoimmune rheumatic diseases - SLE, SSc, IIM, RA.
Expected survival period ≥ 3 months;
Serum creatinine <221.0μmol/L (2.5mg/dl);
AST/ALT below 3 times the upper limit of normal, blood bilirubin <34.2 μmol/L (2.0 mg/dl);
Cardiopulmonary function is basically normal, echocardiography indicates that the ejection fraction is >45%, normal to mild pulmonary hypertension, and the oxygen saturation is above 93% in the resting state without oxygen;
No obvious active infection;
Physical fitness score 0~2 points (ECOG standard);
There are suitable veins for blood cell apheresis or whole blood collection, and there are no contraindications for blood collection;
Women of childbearing age should have a negative serum or urine pregnancy test 48 hours before CAR T cell reinfusion, and agree to take effective contraceptive measures during the trial until the last follow-up;
Voluntary participation and informed consent signed by the patient or his/her legal/authorized representative;

Exclusion criteria

CNS disease-currently active severe CNS, including cerebritis, cerebrovascular accident (CVA), and seizures.
Kidney disease-hemodialysis, Serum creatinine >221.0μmol/L (2.5mg/dl);
Abnormal liver function: aspartate transaminase (AST) or alanine transaminase (ALT) or glutamyl transpeptidase (GGT) detection value is greater than 3 times the upper limit of normal (ULN); or alkaline phosphatase (ALP) or total bilirubin test value greater than 1.5 times the upper limit of normal (ULN); Exceptional: liver function disturbance due to myositis
Cardiovascular disease: Unstable angina or myocardial infarction or coronary artery bypass graft (CABG) within 6 months prior to leukapheresis/ moderate- severe pulmonary hypertension/ severe arrhythmia (ventricular tachycardia, ventricular fibrillation, high grade ventricular block) in the past 6 months; New York heart function class (NYHA) class III- Level IV or LVEF<45%.
Lung disease: patients with interstitial lung disease (ILD) with any of the following: *Requiring O2 therapy and or FVC≤45% of predicted or DLCO≤40% of predicted at screening. * Evidence of pulmonary hypertension as defined as estimated RVSP> 50 mmHg.
Muscle disease: evidence of any of the following: * Severe proximal muscle atrophy of upper or lower extremity on MRI or clinical examination. *Finding of muscular inflammation or myopathy other than the indication, such as inclusion body myositis (IBM), or cancer-associated myositis (myositis diagnosed within 2 years of cancer).
Other uncontrolled diseases: acute diseases (such as acute pneumonia or other infection, pulmonary embolism, diabetic ketoacidosis, acute pancreatitis, etc.) that are clinically unstable or have not been effectively controlled and are not related to SLE/SSc/IIM/RA which in the judgment of the investigator may confound study results or place subjects at undue risk.
Biologics therapy: Received biologic therapy (antibody, inhibitor or agonist) targeting T, B lymphocytes, cytokines or receptors within two months before the study or Rituximab therapy within six months before the study.
Participated in any clinical study within 3 months prior to enrollment, or participate in other clinical investigations during the study period.
Received live vaccine treatment within 30 days prior to Visit 2;
Previous or concurrent malignancy with the following exceptions: Adequately treated basal cell or squamous cell carcinoma, in situ carcinoma of the cervix or breast, treated curatively and without evidence of recurrence for at least 3 years prior to screening. A primary malignancy which has been completely resected, or treated, and is in complete remission for at least 5 years prior to screening.
Transplantation: History of vital organ transplantation (e.g., heart, lung, kidney, liver) or hematopoietic stem cell/or bone marrow transplantation.
HIV positive.
Active hepatitis B or C.
Pregnant or lactating women.
Inability to understand or follow the research protocol subject requirements.
Have any other clinically significant disease history or current disease that, in the judgment of the research physician, may pose a risk to the safety of the subjects, or interfere with the completion of the research procedure and the evaluation of safety and efficacy.