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Clinical Trials in China / NCT07604311
Recruiting Phase 4

Efficacy and Safety of Nefecon on Prevention of Relapse of IgA Nephropathy

NCT07604311 · tracked via the Priya Life Science China tracker
Sponsor
Nanfang Hospital, Southern Medical University
Phase
Phase 4
Started
2026-06-23
Last updated
2026-09-02

Condition(s) studied

IgA Nephropathy (IgAN)

Investigational drug(s) / intervention(s)

NEFECONPlacebo

NEFECON: NEFECON 8mg once daily by mouth for 15 months

Placebo: Placebo oral capsule once daily by mouth for 15 months

Study summary

IgA nephropathy (IgAN) is a chronic progressive kidney disease, and long-term control of proteinuria and prevention of relapse are crucial for delaying disease progression. Patients with IgAN who achieve proteinuria remission after receiving Nefecon for 9 months or longer still face the risk of proteinuria relapse after treatment discontinuation. This study is to evaluate the efficacy and safety of Nefecon 8 mg treatment for 15 months as a maintenance therapy to reduce the risk of IgAN relapse in proteinuria-remitted patients.

Eligibility

Sex
ALL
Min age
18 Years
Max age
75 Years
Healthy volunteers
No
Inclusion Criteria: * Diagnosed primary IgAN with biopsy verification; * Female or male participants ≥18 years of age; * Completion of ≥9 months of Nefecon 16 mg QD at the baseline visit; * Proteinuria ≥ 1g/d prior to initiation of Nefecon; * Proteinuria\<0.5 g/day (or UPCR \<0.5 g/g) at screening and randomization visit; * eGFR ≥30 ml/min/1.73m² at screening; * On stable treatment with supportive treatment (including RAASi, SGLT2i, ERA) for at least 1 month prior to the baseline visit; Exclusion Criteria: * Systemic diseases that may cause mesangial immunoglobulin A deposition, including but not limited to IgA vasculitis nephritis, systemic lupus erythematosus, dermatitis herpetiformis, ankylosing spondylitis, and others; * Type 1 or type 2 diabetes mellitus; * Presence of primary or secondary glomerulopathies (e.g., membranous nephropathy, focal segmental glomerulosclerosis, C3 glomerulopathy and others); * Active infection, severe hepatic impairment (Child-Pugh Class C), congestive heart failure, and malignant tumor within the past 5 years; * On current or planned dialysis or kidney transplantation; * Participants who have been treated with systemic glucocorticoids and immunosuppressive agents within the past 3 months, including mycophenolate mofetil, hydroxychloroquine, cyclophosphamide, azathioprine, leflunomide, calcineurin inhibitors, and Chinese traditional medicines with immunosuppressive effects (such as Tripterygium wilfordii, Sinomenium acutum, Tripterygium Glycosides Tablets, Kunxian Capsules, Kunming Shanhaitang Tablets, etc.); treatment with B-cell targeted biological agents (such as telitacicept and sibeprenlimab, etc.); complement pathway inhibitors, etc.; * Poorly controlled hypertension (resting systolic blood pressure ≥160 mmHg or diastolic blood pressure ≥100 mmHg); * Participants taking potent inhibitors of cytochrome P450 (CYP) 3A4 within the past 1 month, such as ketoconazole, itraconazole, ritonavir, indinavir, saquinavir, erythromycin, or cyclosporine; * Females who are pregnant, breastfeeding, or planning to become pregnant in the trial period. * Any other conditions that, in the investigator's judgment, make the patient ineligible for this clinical study.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Nanfang hospital, Southern Medical University Guangzhou Guangdong Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07604311 on ClinicalTrials.gov ↗ ← All trials in China