- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT07604311
Efficacy and Safety of Nefecon on Prevention of Relapse of IgA Nephropathy (NeFRIN)
30. august 2026 opdateret af: Nanfang Hospital, Southern Medical University
Efficacy and Safety of Nefecon on Prevention of Relapse of IgA Nephropathy: a Randomized, Double-blinded, Placebo-Controlled 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 to reduce the risk of IgAN relapse in proteinuria-remitted patients.
Studieoversigt
Status
Rekruttering
Betingelser
Intervention / Behandling
Undersøgelsestype
Interventionel
Tilmelding (Anslået)
288
Fase
- Fase 4
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiekontakt
- Navn: Fan Fan Hou
- Telefonnummer: +8620 61641591
- E-mail: ffhouguangzhou@163.com
Studiesteder
-
-
Guangdong
-
Guangzhou, Guangdong, Kina, 510515
- Rekruttering
- Nanfang Hospital, Southern Medical University
-
Kontakt:
- Fan Fan Hou
- Telefonnummer: +8620 61641591
- E-mail: ffhouguangzhou@163.com
-
-
Deltagelseskriterier
Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.
Berettigelseskriterier
Aldre berettiget til at studere
- Voksen
- Ældre voksen
Tager imod sunde frivillige
Ingen
Beskrivelse
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.
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Firedobbelt
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
|
Placebo komparator: Styring
Placebo
|
Placebo oral capsule once daily by mouth for 15 months
|
|
Eksperimentel: Treatment arm
NEFECON
|
NEFECON 8mg once daily by mouth for 15 months
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Time to first composite disease relapse
Tidsramme: 15 months
|
either a ≥100% increase in UPCR and an absolute UPCR ≥0.5 g/g, or a ≥30% decline in eGFR from randomization
|
15 months
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
eGFR slope
Tidsramme: 15 months
|
eGFR slope from baseline to Month 15
|
15 months
|
|
Changes in UPCR and 24-hour urinary protein
Tidsramme: 3, 6, 9, 12, and 15 Months
|
Changes in UPCR and 24-hour urinary protein from baseline to Months 3, 6, 9, 12, and 15
|
3, 6, 9, 12, and 15 Months
|
|
Major adverse kidney events
Tidsramme: 15 months
|
The proportion of patients with the first occurrence of major adverse kidney events within 15 months, defined as the occurrence of any one of the following: eGFR ≤15 ml/min/1.73m²,
maintenance dialysis, kidney transplantation, ≥30% decrease in eGFR, or kidney-related death
|
15 months
|
|
The proportion of patients with UPCR ≥0.5 g/g
Tidsramme: 15 months
|
The proportion of patients with sustained UPCR ≥0.5 g/g
|
15 months
|
|
The proportion of patients with UPCR ≥1 g/g
Tidsramme: 15 months
|
The proportion of patients with sustained UPCR ≥1 g/g
|
15 months
|
|
All-cause mortality
Tidsramme: 15 months
|
All-cause mortality
|
15 months
|
Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Datoer for undersøgelser
Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.
Studer store datoer
Studiestart (Faktiske)
23. juni 2026
Primær færdiggørelse (Anslået)
1. december 2028
Studieafslutning (Anslået)
31. december 2028
Datoer for studieregistrering
Først indsendt
18. maj 2026
Først indsendt, der opfyldte QC-kriterier
18. maj 2026
Først opslået (Faktiske)
22. maj 2026
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
2. september 2026
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
30. august 2026
Sidst verificeret
1. august 2026
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- NFEC-2026-268
Plan for individuelle deltagerdata (IPD)
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