A Study of GNC-038 Tetra-specific Antibody Injection in Patients With Systemic Lupus Erythematosus

Inclusion criteria

• Subjects can understand the informed consent form, voluntarily participate in and sign the informed consent form;
• No gender limit;
• Age: ≥18 years old and ≤75 years old;
• Life expectancy greater than 6 months;
• SLE was diagnosed according to the 2019 EULAR/ACR revised criteria;
• Patients with moderate to severe systemic lupus erythematosus, SLEDAI-2K score \&gt at screening; 7 points;
• A stable standard-of-care regimen was maintained for at least 30 days before the first dose;
• ANA ≥ 1:80 or anti-dsdna antibody higher than the upper limit of normal range (ULN) as determined by central laboratory at screening;
• The presence of CD19+ B cells in the peripheral blood of the patient;
• The organ function level before the first administration met the requirements;
• Female subjects of childbearing potential or male subjects with a fertile partner must use highly effective contraception from 7 days before the first dose until 24 weeks after the termination of treatment and should commit not to donate eggs (eggs, oocytes)/sperm for assisted reproduction for 1 year after the last study treatment. Female subjects of childbearing potential must have a negative serum/urine pregnancy test within 7 days before the first dose;
• Participants were able and willing to comply with protocol-specified visits, treatment plans, laboratory tests, and other study-related procedures.

Exclusion criteria

• Severe lupus nephritis within 8 weeks before screening;
• She had uncontrolled lupus crisis within 8 weeks before screening and was not suitable for the study as assessed by the investigator;
• Active encephalopathy or psychosis within 6 months before screening;
• Primary diagnosis of different autoimmune or inflammatory diseases;
• B cell-depleting therapy within 6 months before initiation of GNC-038 treatment;
• Received CAR-T therapy within 6 months before GNC-038 treatment;
• Cytokine-targeting biologic agents used within 12 weeks before dose administration;
• Use of anti-tumor necrosis factor drugs within 8 weeks before administration;
• Use of any JAK inhibitor within 2 weeks before dosing;
• Receipt of any investigational drug within 28 days before dose or within 5 half-lives of the investigational drug;
• Major organ transplantation history or hematopoietic stem cell/bone marrow transplantation;
• Presence of: 1) active hepatitis B at screening; 2) hepatitis C or HIV infection; 3) syphilis infection;
• A history of any cardiovascular disease described in the protocol within 6 months before screening;
• Poorly controlled hypertension (systolic blood pressure ≥160 mmHg or diastolic blood pressure ≥100 mmHg);
• Prolonged QT interval at rest (QTcf \> 450 msec in men or \> 470 msec in women);
• A history of ≥ grade 2 bleeding within 30 days before screening or the need for long-term continuous anticoagulant therapy;
• Patients with a history of allergy to recombinant humanized antibodies or to any of the excipients of GNC-038;
• Women who are pregnant or breastfeeding;
• Have a history or evidence of suicidal thoughts within 6 months before signing ICF, which is considered by the researcher to be a significant risk of suicide;
• Diagnosed with malignant tumor within 5 years before signing ICF;
• Other situations of poor compliance, unwillingness or inability to comply with the study protocol as judged by the investigator;
• History of splenectomy;
• Investigators considered a history of alcohol or drug abuse in the 12 months before screening;
• Any active infection requiring systemic antibiotic treatment within 2 weeks before or during screening;
• A history of severe and/or disseminated viral infection;
• Active M. tuberculosis infection may be present.