Ertugliflozin to reduce arrhythmic burden in ICD/CRT patients (ERASe-trial) - A phase III study.


Journal

American heart journal
ISSN: 1097-6744
Titre abrégé: Am Heart J
Pays: United States
ID NLM: 0370465

Informations de publication

Date de publication:
04 2022
Historique:
received: 24 09 2021
revised: 10 01 2022
accepted: 13 01 2022
pubmed: 20 1 2022
medline: 8 4 2022
entrez: 19 1 2022
Statut: ppublish

Résumé

Sodium glucose cotransporter 2 (SGLT2) have proven profound positive effects in heart failure with reduced ejection fraction (HFrEF). These effects are independent from the presence of diabetes. Metabolic effects, antiinflammatory, and antifibrotic properties are discussed as underlying mechanisms. Despite a strong correlation of ventricular arrhythmias with HFrEF, the impact of ertugliflozin on the ventricular arrhythmic burden has not been investigated, yet. Therefore, the Ertugliflozin to Reduce Arrhythmic burden in ICD ± CRT patientS (ERASe) trial was designed to investigate the efficacy and safety of ertugliflozin in patients with reduced and midrange ejection fraction (EF) with or without diabetes. METHODS: Within a multicentre, national, randomized, double-blind, placebo-controlled, phase 3b trial we aim to enrol a total of 402 patients across Austria. Patients with reduced or midrange EF and ICD ± CRT therapy >3 months and previous ventricular tachycardia (at least 10 documented VT episodes within the last 12 months) are randomized in a 1:1 ratio to ertugliflozin (5 mg once daily orally administered) or matching placebo. The primary endpoint of the ERASe trial is to investigate the impact of ertugliflozin on total burden of ventricular arrhythmias. Further objectives will include number of therapeutic interventions of implanted devices, atrial fibrillation and heart failure biomarkers. CONCLUSION: The ERASe trial will be the first trial to test ertugliflozin in heart failure patients with nonpreserved ejection fraction and ongoing ICD ± CRT therapy regardless of their diabetic status. The ERASe trial may therefore extend the concept of SGLT2 inhibition to improve cardiac remodelling, including reduced arrhythmic burden. Trial registration Identifier EudraCT Nr. 2020-002581-14 / ClinicalTrials.gov Identifier: NCT04600921.

Identifiants

pubmed: 35045327
pii: S0002-8703(22)00007-2
doi: 10.1016/j.ahj.2022.01.008
pii:
doi:

Substances chimiques

Bridged Bicyclo Compounds, Heterocyclic 0
ertugliflozin 6C282481IP

Banques de données

ClinicalTrials.gov
['NCT04600921']
EudraCT
['2020-002581-14']

Types de publication

Clinical Trial, Phase III Journal Article Multicenter Study Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

152-160

Informations de copyright

Copyright © 2022 The Authors. Published by Elsevier Inc. All rights reserved.

Auteurs

Dirk von Lewinski (D)

Medical University of Graz, Department of Internal Medicine, Division of Cardiology, Graz, Austria. Electronic address: dirk.von-lewinski@medunigraz.at.

Norbert J Tripolt (NJ)

Medical University of Graz, Department of Internal Medicine, Interdisciplinary Metabolic Medicine Trials Unit, Division of Endocrinology and Diabetology, Graz, Austria.

Harald Sourij (H)

Medical University of Graz, Department of Internal Medicine, Interdisciplinary Metabolic Medicine Trials Unit, Division of Endocrinology and Diabetology, Graz, Austria.

Peter N Pferschy (PN)

Medical University of Graz, Department of Internal Medicine, Interdisciplinary Metabolic Medicine Trials Unit, Division of Endocrinology and Diabetology, Graz, Austria.

Abderrahim Oulhaj (A)

Institute of Public Health, College of Medicine and Health Sciences, United Arab Emirates University, Abu Dhabi, UAE; Department of Epidemiology and Public Health, College of Medicine and Health Sciences, Khalifa University, Abu Dhabi, UAE.

Hannes Alber (H)

Klinikum Klagenfurt, Abteilung für Innere Medizin und Kardiologie, Austria.

Marianne Gwechenberger (M)

Medical University of Vienna, Department of Cardiology, Vienna, Austria.

Martin Martinek (M)

Ordensklinikum Linz Elisabethinen, Innere Medizin 2 mit Kardiologie, Angiologie und Intensivmedizin, Austria.

Sebastian Seidl (S)

Ordensklinikum Linz Elisabethinen, Innere Medizin 2 mit Kardiologie, Angiologie und Intensivmedizin, Austria.

Deddo Moertl (D)

University Hospital St. Pölten, Department of Internal Medicine III, St.Pölten, Austria.

Michael Nürnberg (M)

Klinik Ottakring, Abteilung für Kardiologie, Wien, Austria.

Franz Xaver Roithinger (FX)

Landesklinikum Wiener Neustadt, Abteilung für Innere Medizin, Kardiologie und Nephrologie, Wiener Neustadt, Austria.

Clemens Steinwender (C)

Kepler University Hospital Linz, Department of Cardiology and Intensive Care Medicine, Linz, Austria.

Markus Stühlinger (M)

Medical University of Innsbruck, University Clinic of Internal Medicine III/Cardiology and Angiology, Innsbruck, Austria.

Andreas Zirlik (A)

Medical University of Graz, Department of Internal Medicine, Division of Cardiology, Graz, Austria.

Martin Benedikt (M)

Medical University of Graz, Department of Internal Medicine, Division of Cardiology, Graz, Austria.

Ewald Kolesnik (E)

Medical University of Graz, Department of Internal Medicine, Division of Cardiology, Graz, Austria.

Markus Wallner (M)

Medical University of Graz, Department of Internal Medicine, Division of Cardiology, Graz, Austria.

Ursula Rohrer (U)

Medical University of Graz, Department of Internal Medicine, Division of Cardiology, Graz, Austria.

Martin Manninger (M)

Medical University of Graz, Department of Internal Medicine, Division of Cardiology, Graz, Austria.

Daniel Scherr (D)

Medical University of Graz, Department of Internal Medicine, Division of Cardiology, Graz, Austria.

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Classifications MeSH