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临床试验/jRCT2031230629
jRCT2031230629招募中不适用

A Phase 2b/3, Multi-part, Randomized, Double-Blinded, Placebo-Controlled Study to Evaluate the Efficacy and Safety of Atacicept in Subjects with IgA Nephropathy (IgAN) (ORIGIN 3)

Vera Therapeutics, Inc.0 个研究点目标入组 36 人开始时间: 2024年5月20日最近更新:

试验速览

阶段
不适用
状态
招募中
入组人数
36
主要终点
-

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Randomized Controlled Trial
干预模型
Parallel Assignment
主要目的
Treatment Purpose
盲法
Double Blind

入排标准

年龄范围
18age old over 至 No limit(—)
性别
All

入选标准

  • Must have the ability to understand and sign a written informed consent form
  • Male or female of >=18 years of age
  • Total urine protein excretion >=1.0 g per 24-hour or urine protein to creatinine ratio (UPCR) >=1.0 mg/mg based on a 24-hour urine sample during the Screening Period
  • Diagnosis of IgAN as demonstrated by renal biopsy conducted within 10 years
  • eGFR >=30 mL/min/1.73 m2, as per the Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI) equation.
  • On a stable prescribed regimen of RAASi for at least 12 weeks that is at the maximum labeled or tolerated dose at Screening
  • Systolic blood pressure <=150 mmHg and less, and diastolic blood pressure <=90 mmHg

排除标准

  • IgAN secondary to another condition (e.g., liver cirrhosis), or other causes of mesangial IgA deposition including IgA vasculitis (i.e., Henoch-Schonlein purpura), systemic lupus erythematosus (SLE), dermatitis herpetiformis, ankylosing spondylitis
  • Total urine protein excretion >= 5g per 24-hour or urine protein to creatinine ratio (UPCR) >= 5 mg/mg based on a 24-hour urine sample during the Screening Period
  • Evidence of rapidly progressive glomerulonephritis (loss of >=50% of eGFR within 3 months of screening)
  • Evidence of nephrotic syndrome within 6 months of screening (serum albumin <30g/L in association with UPCR >3.5 mg/mg
  • Renal or other organ transplantation prior to, or expected during the study
  • Concomitant chronic renal disease in addition to IgAN
  • Uncontrolled diabetes, defined as hemoglobin-A1c (HbA1c) >7.5% at screening
  • History of tuberculosis (TB), untreated latent TB infection (LTBI), or evidence of active TB determined by a positive Quantiferon test
  • Participation in the Phase 2b (Parts A and B) study or any previous treatment with atacicept

结局指标

主要结局

-

Annualized Rate of change in eGFR (ie., annualized eGFR total slope)

次要结局

未报告次要终点

研究者

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