To Assess the Efficacy and Safety of Utilizing Galactose-deficient IgA1 Biomarker Changes to Guide Pathogenic IgA-targeted Therapeutic Strategies
Development and Validation of a Gd-IgA1 Guided Precision Therapy System for Targeted Therapeutic Strategies of IgA Nephropathy: An Open-label, Random Controlled Trial
The goal of this open-label, randomized study is to evaluate the efficacy and safety of the personalized treatment model in which Gd-IgA1 is dynamically monitored to guide medication adjustment in progressive IgAN patients treated with Nefecon or telitacicept.
Researchers will compare two groups of participants: those who have Gd-IgA1 checked regularly during treatment, and those who do not. This is to find out if regular Gd-IgA1 checks can help doctors adjust medication better and get better treatment results.
研究概览
详细说明
IgA nephropathy (IgAN) is the most common primary glomerulonephritis worldwide and a leading cause of end-stage renal disease (ESRD) in young adults. Even with standard supportive care, many patients still experience worsening renal function and eventually develop ESRD.
The widely accepted multi-hit pathogenesis of IgAN recognizes the production of galactose-deficient IgA1 (Gd-IgA1) as the key step. Pathogenic Gd-IgA1 forms immune complexes that deposit in the kidney, triggering inflammation and renal damage, which serves as a target for new regimens.
Two novel targeted therapies have shown positive clinical effects for IgAN:
- Budesonide Enteric Capsules (Nefecon): A gut-targeted oral preparation that releases drugs in the ileocecal region, reducing Gd-IgA1 production and renal immune deposition to protect renal function.
- Telitacicept: A dual Blys/APRIL inhibitor that blocks the proliferation of B cells to reduce pathogenic Gd-IgA1 production.
However, the clinical effects of these novel therapies usually take time to appear (e.g., a significant drop in urinary protein with Nefecon is often seen 3 to 6 months after treatment). Early, sensitive indicators reflecting therapeutic effects are needed to enable timely adjustment of treatment plans.
Biomarkers (e.g., Gd-IgA1) decline earlier than urinary protein, which is highly significant for monitoring early treatment efficacy and optimizing personalized treatment decisions.
研究类型
注册 (估计的)
阶段
- 不适用
联系人和位置
学习联系方式
- 姓名:Yunfei Bao
- 电话号码:086-18500228190
- 邮箱:baoy_fei@163.com
学习地点
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Beijing Municipality
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Beijing、Beijing Municipality、中国、100010
- 招聘中
- Peking University First Hospital
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接触:
- Yunfei Bao
- 电话号码:086-18500228190
- 邮箱:baoy_fei@163.com
-
-
参与标准
资格标准
适合学习的年龄
- 成人
- 年长者
接受健康志愿者
描述
Inclusion Criteria:
- Male or female, between 18 and 75 years age;
- Biopsy confirmed diagnosis of primary IgA nephropathy or IgA Vasculitis-Associated Nephritis;
- Persistent proteinuria, defined as: two separate measurements (with an interval of ≥ 4 weeks) of 24-hour urinary protein excretion (24hUTP) ≥ 0.5 g/day, or urine protein-to-creatinine ratio (UPCR) ≥ 0.44 g/g;
- Estimated glomerular filtration rate (eGFR) (CKD-EPI) ≥ 30 ml/min per 1.73m^2;
- Have received the angiotensin converting enzyme Inhibitors(ACEI) / angiotensin receptor blocker(ARB) standard treatment for 4 weeks prior to randomization;
- Intending to receive or having received Nefecon or telitacicept treatment for ≤ 2 weeks at the time of screening.
Exclusion Criteria:
- Secondary IgA nephropathy (excluding IgA vasculitis) caused by ankylosing spondylitis, systemic lupus erythematosus, viral hepatitis, liver cirrhosis, etc.;
- With a known history or clinical evidence of concurrent renal diseases other than IgA nephropathy;
- Treating with systemic corticosteroids or immunosuppressants including cyclophosphamide, azathioprine, mycophenolate mofetil, tacrolimus, cyclosporine, rituximab, etc. within 3 months prior to randomizing;
- Have initiated or had a dose adjustment of leflunomide, tripterygium wilfordii or hydroxychloroquine within 3 months prior to randomizing;
- Active tuberculosis or latent carrier without treatment;
- Herpes zoster infected patients or patients with positive HIV antibody, positive HCV antibody or HBV infection (According to the HBV screening test, a) the HBsAg-positive; b) HBsAg-negative and HBcAb-positive, the HBV-DNA should be tested to determine the situation: the HBV-DNA positive subjects should be excluded, while the HBV-DNA negative subjects can participated in.)
- Suffering from following gastrointestinal diseases: gastric ulcer bleeding within the past 6 months, active inflammatory bowel disease, a history of major gastrointestinal surgery (e.g., gastrectomy, gastroenterostomy, or bowel resection), or pancreatic injury/pancreatitis within the past 6 months;
- A confirmed history of osteoporosis or osteonecrosis of the femoral head;
- Type 1 or type 2 diabetes with poor glycemic control (HbA1c > 8%);
- Body mass index (BMI) < 18.5 kg/m².;
- Systolic blood pressure (SBP) > 180 mmHg or diastolic blood pressure (DBP) > 110 mmHg;
- Decreased lymphocyte count (absolute value < 1.1 × 10⁹/L) or decreased immunoglobulin G (IgG < 6 g/L).
- Hepatic dysfunction, meeting any of the following: a) Child-Pugh Class C liver dysfunction; b) ALT or AST > 2 × upper limit of normal (ULN), or total bilirubin > 2 × ULN at screening; c) history of hepatic encephalopathy, esophageal varices, or portosystemic shunt surgery;
- Evidence of urinary tract obstruction or dysuria.
- A history of solid organ transplantation, hematopoietic stem cell/cell/bone marrow transplantation, or kidney transplantation.
- Pregnancy, lactation, female participants with childbearing plans during the trial or within 6 months of its completion, and male participants planning to conceive or donate sperm during the trial or within 3 months of its completion;
- With a history of malignant tumors within the past 5 years (excluding cutaneous squamous cell carcinoma or basal cell carcinoma);
- Allergy to human-derived biologics;
- Nephrotoxic drugs is unavoidable during the study period;
- Not suitable for the study judged by investigator.
学习计划
研究是如何设计的?
设计细节
- 主要用途:治疗
- 分配:随机化
- 介入模型:并行分配
- 屏蔽:无(打开标签)
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
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实验性的:Participants who have Gd-IgA1 checked regularly during treatment
Based on the combined results of reductions in urinary protein, Gd-IgA1 levels and other parameters, clinicians can thus evaluate early treatment efficacy and make timely medication adjustments - either continuing the original treatment, increasing the dose, or switching to another medication.
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Participants in the experimental group will undergo a total of five Gd-IgA1 tests at baseline and during the follow-up period, and their clinicians will use these results to guide medication adjustment.
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无干预:Participants who do not have Gd-IgA1 checked during treatment
Clinicians will make medication adjustment base on urinary protein and other laboratory test parameters if necessary.
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研究衡量的是什么?
主要结果指标
结果测量 |
大体时间 |
|---|---|
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Mean change in 24-hour proteinuria from baseline at the end of follow-up
大体时间:From enrollment to the end of follow-up at 12 months
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From enrollment to the end of follow-up at 12 months
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次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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Mean change in 24-hour proteinuria from baseline at the midpoint of follow-up
大体时间:From enrollment to the middle of follow-up period at 6 months
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From enrollment to the middle of follow-up period at 6 months
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Change in estimated glomerular filtration rate (eGFR)
大体时间:From enrollment to the end of follow-up at 12 months
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eGFR is calculated using the CKD-EPI method.
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From enrollment to the end of follow-up at 12 months
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Complete remission of proteinuria
大体时间:From enrollment to the midpoint of follow-up (6 months) and over the entire 12-month follow-up period
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24-hour urine total protein ≤ 0.3 g with a concurrent eGFR decline ≤ 30%
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From enrollment to the midpoint of follow-up (6 months) and over the entire 12-month follow-up period
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Immunosuppressant exposure measures
大体时间:From enrollment to the end of follow-up at 12 months
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Cumulative dosage of non-corticosteroid immunosuppressants, cumulative dosage of systemic corticosteroids converted to prednisone-equivalent dosage, and number of corticosteroid bolus therapy courses during follow-up.
Consecutive daily bolus doses count as one course; topical corticosteroids are excluded.
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From enrollment to the end of follow-up at 12 months
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其他结果措施
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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The incidence rate and severity of adverse events
大体时间:From enrollment to the end of follow-up (12 months)
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An adverse event is any undesirable experience associated with the study intervention in a patient.
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From enrollment to the end of follow-up (12 months)
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合作者和调查者
赞助
研究记录日期
研究主要日期
学习开始 (实际的)
初级完成 (估计的)
研究完成 (估计的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
与本研究相关的术语
其他相关的 MeSH 术语
其他研究编号
- 2025R0625
- 2024YFC2511000 (其他赠款/资助编号:China National Center for Biotechnology Development)
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