Rationale and Design of ATHENA: A Placebo-Controlled, Double-Blind, Parallel Arm Trial to Assess the Efficacy of Dronedarone 400 mg Bid for the Prevention of Cardiovascular Hospitalization or Death from Any Cause in PatiENts with Atrial Fibrillation/Atrial Flutter
Background: Atrial fibrillation (AF) is the most commonly encountered clinical arrhythmia, predominantly affecting elderly patients. There is a continued need for new antiarrhythmic drugs to treat the ever‐increasing number of patients with this arrhythmia. Dronedarone is a new antiarrhythmic compou...
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Published in: | Journal of cardiovascular electrophysiology Vol. 19; no. 1; pp. 69 - 73 |
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Main Authors: | , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
Malden, USA
Blackwell Publishing Inc
01-01-2008
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Subjects: | |
Online Access: | Get full text |
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Summary: | Background: Atrial fibrillation (AF) is the most commonly encountered clinical arrhythmia, predominantly affecting elderly patients. There is a continued need for new antiarrhythmic drugs to treat the ever‐increasing number of patients with this arrhythmia. Dronedarone is a new antiarrhythmic compound currently being developed for treatment of AF.
Methods: The ATHENA trial (A placebo‐controlled, double‐blind, parallel arm Trial to assess the efficacy of dronedarone 400 mg bid for the prevention of cardiovascular Hospitalization or death from any cause in patiENts with Atrial fibrillation/atrial flutter) is the largest single antiarrhythmic drug trial ever conducted. More than 4,600 patients with a history of AF or atrial flutter (AFL) have been randomized to receive dronedarone 400 mg bid or matching placebo. The primary study endpoint is time to first cardiovascular hospitalization or death from any cause. The study has completed patient enrollment in December 2006 and is expected to end follow‐up 1 year later.
Conclusion: ATHENA will be the largest efficacy and safety trial of dronedarone, a multichannel blocker compound with properties from class I, II, III, and IV antiarrhythmic drugs developed to treat patients with AF. |
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Bibliography: | istex:878D8FE1B54791EEA8EE0B7E63BBD592251522BE ark:/67375/WNG-08HM9V65-0 ArticleID:JCE1016 This manuscript was processed by a guest editor. Dr. Seiz is an employee of sanofi‐aventis. Research support from sanofi‐aventis was received by Drs. Hohnloser, Connolly, Crijns, and Torp‐Petersen. Drs. Hohnloser, Connolly, Crijns, Page, and Torp‐Petersen received honoraria and/or consulting fees from sanofi‐aventis. Manuscript received 24 May 2007; Revised manuscript received 26 July 2007; Accepted for publication 30 July 2007. ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-News-1 ObjectType-Feature-3 content type line 23 |
ISSN: | 1045-3873 1540-8167 |
DOI: | 10.1111/j.1540-8167.2007.01016.x |