A Study of RD06-04 in Patients With Active Autoimmune Diseases

NCT ID: NCT06548620

Last Updated: 2024-08-12

Basic Information

• Recruitment Status: NOT_YET_RECRUITING
• Clinical Phase: EARLY_PHASE1
• Total Enrollment: 18 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2024-08-31
• Study Completion Date: 2027-08-31

Brief Summary

This is an open-label, Phase I, investigator-initiated trial (IIT) aimed at evaluating the safety, tolerability, pharmacokinetics, pharmacodynamics, and efficacy of RD06-04 in patients with autoimmune diseases mediated by autoantibodies. The study population includes patients with Systemic Lupus Erythematosus (SLE), Systemic Sclerosis (SSc), ANCA-Associated Vasculitis (AAV), Idiopathic Inflammatory Myopathy (IIM), Sjögren's Syndrome (SS), Multiple Sclerosis (MS), Neuromyelitis Optica Spectrum Disorder (NMOSD), and Myasthenia Gravis (MG).

Conditions

SLE (Systemic Lupus); Sclerosis; ANCA Associated Vasculitis; IIM; SS; MS; NMO Spectrum Disorder; MG

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

RD06-04 cell infusion

Group Type: EXPERIMENTAL

RD06-04 cell infusion

Intervention Type: DRUG

CAR T Cells

Interventions

RD06-04 cell infusion

CAR T Cells

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. The subjects voluntarily participated in the study and signed the informed consent form.

2. Age ≥18 years old and ≤70 years old, both sexes.

3. Organ function and laboratory tests:

1. Liver function: alanine aminotransferase (ALT) and aspartate aminotransferase (AST) ≤3× upper limit of normal (ULN), total bilirubin (TBIL) ≤2×ULN (except Gilbert's syndrome).

2. Renal function: creatinine ≤1.5×ULN or creatinine clearance ≥40 ml/min.

3. Blood routine: neutrophil count ≥1×109/L, hemoglobin ≥60g/L, platelet count ≥20×109/L, lymphocyte count >0.3×109/L.

4. Coagulation: international normalized ratio (INR) ≤ 1.5×ULN, or prothrombin time (PT) ≤ 1.5×ULN.

5. Oxygen saturation (SpO2) ≥92% at rest in room air.

6. Left ventricular ejection fraction (LVEF) ≥50% on echocardiography.

4. Negative serum or urine pregnancy test results in female subjects of childbearing potential at screening.

5. Women of childbearing potential must agree to use a highly effective method of contraception for at least 28 days before initiation of elution and up to 12 months after RD06-04 reinfusion. Men of childbearing potential had to agree to the use of an effective barrier method of contraception from the initiation of lymphoidectomy until 12 months after reinfusion of RD06-04 and had to refrain from donating semen or sperm throughout the trial.

1. A definitive diagnosis of SLE according to the 2019 European League Against Rheumatism (EULAR) / American College of Rheumatology (ACR) classification criteria or the 2012 Systemic Lupus International Collaborating Clinics (SLICC) criteria.

2. Positive antinuclear antibodies (ANA) at screening, and/or positive anti-double-stranded DNA (anti-dsDNA) antibodies, and/or positive anti-Smith antibodies.

3. A SLEDAI-2K score >6 at screening, and a 'clinical' SLEDAI-2K score ≥4.

1. Diagnosed with SSc according to the 2013 ACR/EULAR classification criteria.

2. Diagnosed with diffuse cutaneous SSc at screening, with a disease duration ≤5 years.

1. Meeting the diagnostic criteria for ANCA-associated vasculitis established by the 2022 ACR/EULAR, including Microscopic Polyangiitis (MPA), Granulomatosis with Polyangiitis (GPA), and Eosinophilic Granulomatosis with Polyangiitis (EGPA).

2. Positive testing for ANCA-associated antibodies in the past or at screening (specifically, positive anti-myeloperoxidase antibodies, MPO-ANCA, or positive anti-proteinase 3 antibodies, PR3-ANCA).

1. Diagnosed with IIM according to the 2017 ACR/EULAR classification criteria (including probable or definite diagnosis, i.e., probability ≥55%), including subtypes such as Dermatomyositis (DM), Anti-Synthetase Syndrome (ASS), and Immune-Mediated Necrotizing Myopathy (IMNM).

2. Patients in the active phase, defined as those with at least 2 of the following six core set measures being abnormal: decreased muscle strength (MMT-8 <142), Physician Global Assessment (PhGA, 10cm VAS) ≥2cm, Patient Global Assessment (PtGA, 10cm VAS) ≥2cm, Extramuscular Disease Activity Total Score (assessed using the MDAAT scoring tool) ≥2cm, Health Assessment Questionnaire (HAQ) ≥0.25, and Creatine Kinase (CK) muscle enzyme levels ≥1.5×ULN

1. Diagnosed with primary Sjögren's Syndrome according to the 2016 ACR/EULAR classification criteria.

2. Positive for anti-SSA/Ro antibodies detected in the past or at screening.

3. A score of ≥6 on the European League Against Rheumatism Sjögren's Syndrome Disease Activity Index (ESSDAI) at screening.

1. Diagnosed with Relapsing-Remitting Multiple Sclerosis (RMS) according to the revised McDonald criteria of 2017, including Clinically Isolated Syndrome, Relapsing-Remitting MS (RRMS), and active Secondary Progressive MS.

2. Expanded Disability Status Scale (EDSS) score is ≤5.

1. Meeting the diagnostic criteria for NMOSD established by the International Panel for NMO Diagnosis (IPND) in 2015.

2. Positive Aquaporin-4 Immunoglobulin G (AQP4-IgG) during the screening period or positive AQP4-IgG in previous medical records.

1. Patients diagnosed with generalized myasthenia gravis.

2. Clinical classification of II, III, or IV by the Myasthenia Gravis Foundation of America (MGFA).

3. Positive serological tests for acetylcholine receptor antibodies (AChR-Ab) or muscle-specific receptor tyrosine kinase antibodies (MuSK-Ab) or low-density lipoprotein receptor-related protein 4 antibodies (LRP4-Ab) at screening, or positive records of AChR-Ab, MuSK-Ab, or LRP4-Ab in previous medical history.

Exclusion Criteria

1. SLE Patients: Those with uncontrolled lupus crisis within the 8 weeks prior to screening, including rapidly progressive lupus nephritis, severe neuropsychiatric lupus, severe hemolytic anemia, severe immune thrombocytopenia, agranulocytosis, severe cardiac damage, severe lupus pneumonia, severe lupus hepatitis, and severe vasculitis, as assessed by the investigator as unsuitable to participate in this study.

2. IIM Patients: Presence of severe rhabdomyolysis or CK levels ≥120×ULN at screening.

3. MG Patients: Presence of uncontrolled myasthenia gravis crisis within 2 weeks prior to screening.

4. Patients with severe asthma or Chronic Obstructive Pulmonary Disease (COPD) are eligible. Patients with mild or moderate asthma or COPD who are receiving stable treatment can also be enrolled.

5. There has been an active infection requiring systemic treatment within 2 weeks prior to the urethral irrigation, such as infectious pneumonia, tuberculosis, etc.

6. Positive for hepatitis B surface antigen (HBsAg), or positive for hepatitis B core antibody (HBcAb) with detectable hepatitis B virus (HBV) DNA in peripheral blood; positive for hepatitis C virus (HCV) antibody with detectable HCV RNA in peripheral blood; positive for human immunodeficiency virus (HIV) antibody; positive for syphilis antibody.

7. Pregnant or breastfeeding women.

8. Any condition that, in the investigator's opinion, may affect study participation, pose a safety risk to the patient, or potentially confound the interpretation of study results.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 70 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Nanjing Bioheng Biotech Co., Ltd.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

The First Affiliated Hospital of Zhengzhou University

Zhengzhou, Henan, China

Countries

China

Central Contacts

PENG YU

Role: CONTACT

peng.yu@bioheng.com

18451117657

Ming Gao

Role: CONTACT

ming.gao@bioheng.com

17714188689

Facility Contacts

Yi Zhang, PhD

Role: primary

yizhang@zzu.edu.cn

151 3892 8971

Xuan Zhao, PhD

Role: backup

zhaoxuan929@foxmail.com

135 9889 9029

Other Identifiers

BHCT-RD06-04-04

Identifier Type: -

Identifier Source: org_study_id