A Study to Assess Effectiveness and Safety of Efgartigimod in Chinese Patients With Lupus Nephritis (ZL-1103-013)

Prior treatment

• Currently on renal dialysis or expected to require dialysis during study period
• Previous kidney transplantation or planned transplantation during study period
• Previously failed treatment with MMF or any form of mycophenolate-based induction therapy, based on the investigator's opinion
• Use of complementary therapies, including Traditional Chinese Medicine, herbs, or procedure (eg, acupuncture) that can potentially interfere with the efficacy and safety of participants as assessed by the investigator

Other illness

• Active or chronic infection requiring treatment
• Any evidence of central nervous system lupus (including but not limited to seizures, psychosis, organic brain syndrome, cerebrovascular accident, cerebritis, or CNS vasculitis)
• Heart failure due to Systemic Lupus Erythematodes, or any other severe cardiovascular involvement with safety concerns according to investigator's judgment
• Any other known autoimmune disease that would interfere with an accurate assessment of clinical symptoms of SLE/LN or put the participant at undue risk
• Known hypersensitivity or contraindication to efgartigimod, any excipient of the IMP, or SoC medication used in the study
• In the opinion of the investigator, current or history of (ie, within 12 months of randomization) alcohol, drug, or medication abuse
• Any conditions or circumstances that in the opinion of the investigator may make the participant unsuitable for the study
  • The full list of criteria can be found in the protocol.

Age

• History of malignancy unless deemed cured by adequate treatment with no evidence of recurrence for ≥3 years before randomization. The following cancers are not exclusionary: basal cell or squamous cell skin cancer; carcinoma in situ of the cervix; carcinoma in situ of the breast; incidental histological finding of prostate cancer

Other

• SARS-CoV-2 antigen-based positive test at screening. The test is required regardless of whether the participant has been vaccinated
• Pregnant or lactating females and those who intend to become pregnant during study participation

• Aged ≥18 years when signing the informed consent form (ICF)
• Capable of providing signed informed consent, and complying with protocol requirements
• Diagnosis of SLE according to the Systemic Lupus Erythematosus International Collaborating Clinic (SLICC) 2012 classification criteria
• Active, proliferative LN Class III or IV \[excluding Class III (C), IV-S (C), and IV-G (C)\], either with or without the presence of Class V using the 2003 International Society of Nephrology (ISN)/Renal Pathology Society (RPS) criteria, proven by kidney biopsy within 6 months before randomization and confirmed by the central biopsy reading group
• Require LN induction therapy (glucocorticoids and MMF/MPA) based on investigator's clinical judgment. Induction therapy may begin before screening but should be initiated within 60 days before randomization
• Agree to use contraceptives consistent with local regulations. Full inclusion criteria can be found in the protocol