Immunoglobulin A Nephropathy
Conditions
Interventions
Sibeprenlimab 400mg or Placebo s.c. q 4 week
Sponsors
Kuwada Anna
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: - Male and female patients >= 18 years of age . - Biopsy-confirmed IgAN. (Patients with an eGFR of 30 to 45 mL/min/1.73m2 must have had a kidney biopsy performed within 36 months of the screening visit). - Stable and maximally tolerated dose of ACEI and/or ARB for at least 3 months prior to screening. Patients who are on a stable dose of SGLT2i may participate if treatment was initiated >= 3 months prior to screening. Patients who are unable to take an ACEI or ARB may participate if their overall management conforms with standards of care and other protocol requirements. - Screening urine protein/creatinine ratio (uPCR) >= 0.75 g/g or urine protein >= 1.0 g/day - eGFR >= 30 mL/min/1.73 m2, (for the exploratory cohort only: eGFR 20- <30 mL/min/1.73 m2), calculated using the CKD-EPI equation.)
Exclusion criteria
Exclusion criteria: - Secondary forms of IgAN or IgA vasculitis. - Coexisting chronic kidney disease other than IgAN. - Kidney biopsy findings in addition to IgAN including those of diabetic nephropathy, membranous nephropathy, or lupus nephritis. Hypertensive vascular changes are acceptable. - Kidney biopsy MEST or MEST-C score of T2 or C2 (Oxford IgAN classification). If MEST-scoring was not performed, the presence of > 50% tubulo-interstitial fibrosis, or crescents in > 25% of glomeruli is exclusionary. This does not apply to the exploratory cohort. - Nephrotic syndrome - Serum IgG < 600 mg/dL at screening. - Chronic systemic immunosuppression, including glucocorticoids, within 16 weeks of randomization - Participation in another interventional clinical trial and receipt of another investigational drug within 30 days prior to the administration of IMP or 5 half-lives from last investigational drug administration, whichever is longer. - Chronic infectious disease, or acute infectious disease at time of screening. - Type 1 diabetes, or poorly controlled Type 2 diabetes - Uncontrolled hypertension
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Primary Efficacy: Ratio of uPCR at 9 months compared with baseline, based on 24-hour urine collection. | — |
Countries
Argentina, Australia, Belgium, Brazil, Canada, China, Croatia, Czech Republic, France, Germany, Greece, Hong Kong, Hungary, India, Israel, Italy, Japan, Korea, Malaysia, Netherlands, Philippines, Poland, Portugal, Singapore, Spain, Sri Lanka, Taiwan, Thailand, United Kingdom, United States, Vietnam
Contacts
Public ContactAnna Kuwada
Syneos Health Japan K.K.
Outcome results
None listed