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临床试验/CTRI/2022/11/047572
CTRI/2022/11/047572进行中(未招募)3 期

A Phase 3, Multicenter, Randomized, Double-blind, Placebo-controlled Trial to Evaluatethe Efficacy and Safety of Sibeprenlimab Administered Subcutaneously in Subjects with Immunoglobulin A Nephropathy - VISIONARY

Otsuka Pharmaceutical Development Commercialization Inc0 个研究点目标入组 0 人开始时间: 待定最近更新:

试验速览

阶段
3 期
状态
进行中(未招募)

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

入选标准

  • •1. Male and female patients = 18 years of age.
  • •2. 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).
  • •3. 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.
  • •4. Screening urine protein/creatinine ratio (uPCR) = 0.75 g/g or urine protein = 1.0 g/day
  • •5. eGFR = 30 mL/min/1.73 m2, (for the exploratory cohort only: eGFR 20- <30 mL/min/1.73 m2), calculated using theCKD-EPI equation.)

排除标准

  • •1. Secondary forms of IgAN or IgA vasculitis.
  • •2. Coexisting chronic kidney disease other than IgAN.
  • •3. Kidney biopsy findings in addition to IgAN including those of diabetic nephropathy, membranous nephropathy, or lupus nephritis. Hypertensive vascular changes are acceptable.
  • •4. 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.
  • •5. Nephrotic syndrome
  • •6. Serum IgG < 600 mg/dL at screening.
  • •7. Chronic systemic immunosuppression, including glucocorticoids, within 16 weeks of randomization
  • •8. 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.
  • •9. Chronic infectious disease, or acute infectious disease at time of screening.
  • •10. Type 1 diabetes, or poorly controlled Type 2 diabetes
  • •11. Uncontrolled hypertension
  • •The protocol provides additional information about these and other inclusion and exclusion criteria.

研究者

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