Your browser doesn't support javascript.
loading
Selonsertib in Patients with Diabetic Kidney Disease: A Phase 2b Randomized Active Run-In Clinical Trial.
Heerspink, Hiddo J L; Perkovic, Vlado; Tuttle, Katherine R; Pergola, Pablo E; Mahaffey, Kenneth W; Patel, Uptal D; Ishida, Julie H; Kuo, Albert; Chen, Fang; Kustra, Robert; Petrovic, Vladimir; Rossing, Peter; Kashihara, Naoki; Chertow, Glenn M.
Afiliação
  • Heerspink HJL; Department of Clinical Pharmacy and Pharmacology, University Medical Center, University of Groningen, Groningen, Netherlands.
  • Perkovic V; The George Institute for Global Health, Sydney, Australia.
  • Tuttle KR; UNSW Sydney, Sydney, Australia.
  • Pergola PE; University of Washington School of Medicine, Department of Medicine, Nephrology Division, Seattle, WA, and Providence Inland Northwest Health, Providence Medical Research Center, Spokane, Washington.
  • Mahaffey KW; Renal Associates PA, San Antonio, Texas.
  • Patel UD; Stanford Center for Clinical Research, Department of Medicine, Stanford University School of Medicine, Stanford, California.
  • Ishida JH; Department of Clinical Development, Gilead Sciences, Inc., Foster City, California.
  • Kuo A; Complications Research, Steno Diabetes Center Copenhagen, Copenhagen, Denmark.
  • Chen F; Department of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark.
  • Kustra R; Kawasaki Medical School, Kurashiki, Japan.
  • Petrovic V; Departments of Medicine, Epidemiology and Population Health, and Health Policy, Stanford University School of Medicine, Stanford, California.
  • Rossing P; UNSW Sydney, Sydney, Australia.
  • Kashihara N; University of Washington School of Medicine, Department of Medicine, Nephrology Division, Seattle, WA, and Providence Inland Northwest Health, Providence Medical Research Center, Spokane, Washington.
  • Chertow GM; Renal Associates PA, San Antonio, Texas.
J Am Soc Nephrol ; 2024 Jul 17.
Article em En | MEDLINE | ID: mdl-39018154
ABSTRACT

BACKGROUND:

Selonsertib is an apoptosis signal-regulating kinase 1 inhibitor that reduces inflammation, fibrosis, and apoptosis. The MOSAIC study evaluated whether selonsertib attenuated kidney function decline in patients with diabetic kidney disease.

METHODS:

We conducted a phase 2b study in adults with type 2 diabetes and eGFR 20 to <60 ml/min/1.73 m2 with UACR 150 to 5000 mg/g on maximum tolerated dose of ACE inhibitor or ARB. To account for an acute selonsertib-related decrease in eGFRcr, patients entered a 4-week selonsertib run-in period to establish treatment-specific baseline eGFRcr. Patients were randomized 11 to selonsertib 18 mg or matching placebo once daily. We followed all participants up until the last randomized participant completed 48 weeks follow-up. The primary efficacy outcome was the difference in eGFRcr slopes from treatment-specific baselines to week 84, evaluated at a prespecified two-sided P = 0.30. We also evaluated kidney clinical events (eGFRcr ≥40% decline from pre-run-in baseline, kidney failure, or death due to kidney disease) and adverse events.

RESULTS:

In total, 310 patients were randomized (selonsertib n=154, placebo n=156; 68% male, mean age 65 years, mean baseline eGFRcr 35 ml/min/1.73 m2). Mean difference between selonsertib and placebo eGFRcr slopes at week 84 was 1.20 ml/min/1.73 m2/year (95% CI, -0.41 to 2.81; P = 0.14). Kidney clinical events occurred in 17% (26/154) of patients randomized to selonsertib and 12% (19/156) of those randomized to placebo (difference 4.7%; 95% CI, -6.3% to 15.9%). The most common investigator-reported adverse event was acute kidney injury (selonsertib 11.0/100 and placebo 5.9/100 patient-years).

CONCLUSIONS:

Selonsertib attenuated the decline in eGFRcr over up to 84 weeks; however, it resulted in a numerically higher number of patients reaching a kidney clinical event and a numerically higher rate of investigator-reported acute kidney injury.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article