ArticleInternational urology and nephrology2026
Nefecon in IgA nephropathy: real-world renal efficacy, safety profile, and treatment response from a 9-month retrospective cohort analysis.
Article in International urology and nephrology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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Who cites it
1 citing paper in PubMed.
- Real-world multicenter evidence on Nefecon for attenuating proteinuria and kidney function decline in IgA nephropathy.Frontiers in immunology · 2026Observational
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5 authors.
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Abstract
objectiveTo evaluate the real-world clinical efficacy and safety of Nefecon, a targeted-release formulation of budesonide, in patients with IgA nephropathy (IgAN).
methodsRetrospective cohort analysis of 40 biopsy-confirmed IgAN patients receiving Nefecon 16 mg/day. PRIMARY ENDPOINT: change in proteinuria at 9 months. Secondary endpoints: eGFR trajectory, remission rates, and safety.
resultsAt 9 months, proteinuria decreased from 2.24 ± 1.64 to 0.69 ± 0.59 g/day (60.2% reduction; p < 0.001), with 85% and 72.5% of patients achieving ≥ 30% and ≥ 50% reductions, respectively. Mean eGFR improved from 49.5 ± 22.6 to 53.6 ± 27.6 mL/min/1.73 m
conclusionIn real-world practice, Nefecon demonstrates significant efficacy in reducing proteinuria, improving renal function, and achieving high remission rates in IgAN patients over 9 months, with a favorable safety profile. Subgroup analyses highlight that baseline renal function, proteinuria severity, biopsy interval, and combination with immuno-suppressants may influence treatment response. Larger prospective studies are needed to validate these findings.
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Registered trials
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