Abstract: SA-OR93
Semaglutide Reduced Risks of Major Kidney Outcomes Irrespective of CKD Severity in the FLOW Trial
Session Information
- High-Impact Clinical Trials - 2
October 26, 2024 | Location: Hall D, Convention Center
Abstract Time: 11:15 AM - 11:30 AM
Category: Diabetic Kidney Disease
- 702 Diabetic Kidney Disease: Clinical
Authors
- Tuttle, Katherine R., Providence Health and Services, Spokane, Washington, United States
- Mann, Johannes F., KfH Nierenzentrum fur Kinder und Jugendliche Munster, Munster, Nordrhein-Westfalen, Germany
- Sokareva, Ekaterina, Novo Nordisk A/S, Bagsvaerd, Hovedstaden, Denmark
- Rayner, Brian, Groote Schuur Hospital, Observatory, South Africa
- Pugliese, Giuseppe, Universita degli Studi di Roma La Sapienza, Rome, Lazio, Italy
- Pratley, Richard E., AdventHealth Central Florida, Orlando, Florida, United States
- Perkovic, Vlado, University of New South Wales, Sydney, New South Wales, Australia
- Mahaffey, Kenneth W., Stanford University School of Medicine, Stanford, California, United States
- Kashihara, Naoki, Kawasaki Ika Daigaku, Kurashiki, Okayama, Japan
- Jeppesen, Ole K., Novo Nordisk A/S, Bagsvaerd, Hovedstaden, Denmark
- Gumprecht, Janusz, Slaski Uniwersytet Medyczny w Katowicach Wydzial Nauk Medycznych w Zabrzu, Zabrze, Województwo śląskie, Poland
- Correa-Rotter, Ricardo, Instituto Nacional de Ciencias y Nutrition Salvador Zubiran, Ciudad de Mexico, Mexico City, Mexico
- Cherney, David, Toronto General Hospital, Toronto, Ontario, Canada
- Bosch-Traberg, Heidrun, Novo Nordisk A/S, Bagsvaerd, Hovedstaden, Denmark
- Arici, Mustafa, Hacettepe Universitesi, Ankara, Ankara, Turkey
- Rossing, Peter, Steno Diabetes Center Copenhagen, Herlev, Capital Region of Denmark, Denmark
Background
Semaglutide reduced risks of major kidney outcomes, cardiovascular (CV) events, and death from any cause in participants with type 2 diabetes (T2D) and chronic kidney disease (CKD) in the FLOW trial. The aim of this analysis was to assess kidney outcomes by baseline CKD severity.
Methods
Participants had T2D with eGFR 50–75 mL/min/1.73m2 and urine albumin–creatinine ratio (UACR) >300–<5000 mg/g, or eGFR 25–<50 mL/min/1.73m2 and UACR >100–<5000 mg/g. They were randomized to subcutaneous semaglutide 1 mg once weekly or placebo. The FLOW primary outcome was a composite of kidney failure (initiation of chronic kidney replacement therapy, eGFR <15 ml/min/1.73m2), >50% eGFR decline, or death due to kidney or CV causes. Participants were categorized by baseline eGFR and UACR.
Results
Among 3533 participants, 30% (n=1069) were women. At baseline, their mean age was 67 years, mean eGFR was 47 mL/min/1.73 m2, and median UACR was 568 mg/g. The hazard ratio for the primary outcome was 0.76 (95% CI 0.66–0.88) for semaglutide versus placebo over a median of 3.4 years. Consistent results were observed across eGFR and UACR categories (Figure).
Conclusion
Semaglutide safely reduced risks of major kidney outcomes irrespective of CKD severity defined by baseline eGFR or UACR in participants with T2D and CKD in the FLOW trial.
Funding
- Commercial Support – Novo Nordisk