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A Trial to Evaluate the Long-term Safety and Tolerability of HRS-5965 in Patients With Primary IgA Nephropathy

RecruitingPhase 2Ages 18 Years - anyAllChengdu Suncadia Medicine Co., Ltd.
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In plain words

What the trial is, and whether it could suit you

This study aims to evaluate the long-term safety of HRS-5965 capsules in patients with primary IgA nephropathy, and also to assess its efficacy in reducing 24-hour urinary protein and delaying the decline in eGFR in these patients.

Sign in to get the eligibility rules as simple questions to take to your doctor.

📋 Eligibility rules (as published)
Inclusion Criteria: 1. Patients with primary IgA nephropathy who completed treatment in Study HRS-5965-305, or who prematurely discontinued study drug during the maintenance phase following initiation of rescue therapy; 2. Understand the research procedures and methods, voluntarily participate in this trial and sign the informed consent form in person. Exclusion Criteria: 1. Hypersensitivity to the study drug or its components; 2. History of immunodeficiency disorders; 3. History of invasive encapsulated bacterial infection; 4. History of malignant neoplasm; 5. The estimated glomerular filtration rate (eGFR) is less than 20 mL/min/1.73m2;
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What it tests

  • HRS-5965 Capsules
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Where

1 site
Peking University First Hospital
Beijing, China
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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