GlomCon Hawaii 2026 Abstracts

period, with an 8-week safety follow-up.The key secondary endpoint was the annualized slope (from week 4) of estimated glomerular filtration rate (eGFR) over 24 months.Secondary endpoints included change in eGFR from baseline at 24 months and safety.A post hoc analysis evaluated annualized eGFR slope from baseline through 24 months.Results In total, 510 patients were randomized (sibeprenlimab, n = 259; placebo, n = 251).The annualized eGFR slope estimated over 24 months was 0.3 mL/min/1.73m 2 / yr (95% CI, -0.4 to 0.9) with sibeprenlimab and -4.2 mL/min/1.73m 2 /yr (95% CI, -4.9 to -3.6) with placebo (treatment difference: 4.5 mL/min/1.73m 2 /yr; 95% CI, 3.6 to 5.4; P < 0.0001).The least-squares mean treatment difference for eGFR change from baseline was 9.2 mL/ min/1.73m 2 (95% CI, 7.1 to 11.4; P < 0.0001).Post hoc analysis of annualized eGFR slope estimated from baseline demonstrated a treatment difference of 4.7 mL/min/1.73m 2 /yr (95% CI, 3.8 to 5.6).Sibeprenlimab was well tolerated, with safety comparable to placebo, consistent with previously communicated interim results.Conclusions Sibeprenlimab stabilized kidney function over 24 months with a favorable safety profile.

Publication Details

Journal
Rare Kidney Diseases
Published
2026-09-15
DOI
https://doi.org/10.1007/s44531-026-00010-6
Primary Topic
Renal Diseases and Glomerulopathies
Type
article
Field-Weighted Citation Impact
0.00

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GlomCon Hawaii 2026 Abstracts

Rare Kidney Diseases
Renal Diseases and Glomerulopathies
article

GlomCon Hawaii 2026 Abstracts

article en

Abstract

period, with an 8-week safety follow-up.The key secondary endpoint was the annualized slope (from week 4) of estimated glomerular filtration rate (eGFR) over 24 months.Secondary endpoints included change in eGFR from baseline at 24 months and safety.A post hoc analysis evaluated annualized eGFR slope from baseline through 24 months.Results In total, 510 patients were randomized (sibeprenlimab, n = 259; placebo, n = 251).The annualized eGFR slope estimated over 24 months was 0.3 mL/min/1.73m 2 / yr (95% CI, -0.4 to 0.9) with sibeprenlimab and -4.2 mL/min/1.73m 2 /yr (95% CI, -4.9 to -3.6) with placebo (treatment difference: 4.5 mL/min/1.73m 2 /yr; 95% CI, 3.6 to 5.4; P < 0.0001).The least-squares mean treatment difference for eGFR change from baseline was 9.2 mL/ min/1.73m 2 (95% CI, 7.1 to 11.4; P < 0.0001).Post hoc analysis of annualized eGFR slope estimated from baseline demonstrated a treatment difference of 4.7 mL/min/1.73m 2 /yr (95% CI, 3.8 to 5.6).Sibeprenlimab was well tolerated, with safety comparable to placebo, consistent with previously communicated interim results.Conclusions Sibeprenlimab stabilized kidney function over 24 months with a favorable safety profile.

Rare Kidney DiseasesVol. 1(S1)
Ohio State University, University of Leicester, University of Toronto, Department of Medicine, University of Toronto
Openalex Percentile: Top 11%
Renal Diseases and Glomerulopathies
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GlomCon Hawaii 2026 Abstracts · Rare Kidney Diseases (2026) | TGRS Research Map | TGRS