Efficacy and Safety of Nefecon on Prevention of Relapse of IgA Nephropathy: a Randomized, Double-blinded, Placebo-Controlled Trial

Trial statusNot yet recruiting
Trial phasePhase 4
Trial typeInterventional
Biological sexAll
Age18+
SponsorNanfang Hospital, Southern Medical University

About this trial

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 for prevention of proteinuria relapse in proteinuria-remitted patients.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

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

Disqualifiers

Systemic diseases that may cause mesangial immunoglobulin A deposition, including but not limited to IgAVN, systemic lupus erythematosus, dermatitis herpetiformis, ankylosing spondylitis, and others;

Presence of other glomerulopathies (e.g., C3 glomerulopathy, nephrotic syndrome and/or diabetes nephropathy), active infection, severe hepatic impairment (Child-Pugh Class C), congestive heart failure, and a history of 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, etc.); complement pathway inhibitors, etc.;

Trial design

Design model

Parallel

Treatments tested in this trial

  • NEFECON

    Drug

    NEFECON 8mg once daily by mouth for 15 months

  • Placebo

    Drug

    Placebo oral capsule once daily by mouth for 15 months

Treatment groups

288 Participants
are divided into 2 treatment groups
Group A: ControlPlacebo comparator 1 intervention
Group B: Treatment armExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Time to first occurrence of proteinuria relapse

≥100% increase in UPCR and UPCR ≥0.5 g/g, separated by at least 1 week

Time frame
15 months

Secondary outcomes

1

eGFR slope

eGFR slope from baseline to Month 15

Time frame
15 months
2

The proportion of patients with UPCR ≥0.5 g/g

The proportion of patients with UPCR ≥0.5 g/g within 15 months

Time frame
15 months
3

The proportion of patients with UPCR ≥1 g/g

The proportion of patients with UPCR ≥1 g/g within 15 months

Time frame
15 months
4

Changes in UPCR and 24-hour urinary protein

Changes in UPCR and 24-hour urinary protein from baseline to Months 3, 6, 9, 12, and 15

Time frame
3, 6, 9, 12, and 15 Months

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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