Celivarone for Maintenance of Sinus Rhythm and Conversion of Atrial Fibrillation/Flutter

Celivarone in Atrial Fibrillation/Atrial Flutter. Introduction: Celivarone, a new noniodinated benzofuran derivative pharmacologically related to dronedarone and amiodarone, has been shown to have antiarrhythmic properties at a molecular level. The purpose of the 2 trials presented here (MAIA and CO...

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Published inJournal of cardiovascular electrophysiology Vol. 23; no. 5; pp. 462 - 472
Main Authors KHITRI, AVINASH R., ALIOT, ETIENNE M., CAPUCCI, ALESSANDRO, CONNOLLY, STUART J., CRIJNS, HARRY, HOHNLOSER, STEFAN H., KULAKOWSKI, PIOTR, ROY, DENIS, RADZIK, DAVID, KOWEY, PETER R.
Format Journal Article
LanguageEnglish
Published Malden, USA Blackwell Publishing Inc 01.05.2012
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Summary:Celivarone in Atrial Fibrillation/Atrial Flutter. Introduction: Celivarone, a new noniodinated benzofuran derivative pharmacologically related to dronedarone and amiodarone, has been shown to have antiarrhythmic properties at a molecular level. The purpose of the 2 trials presented here (MAIA and CORYFEE) was to assess celivarone efficacy in the maintenance of sinus rhythm postcardioversion and for the conversion of atrial fibrillation (AF)/atrial flutter (AFL). Methods and Results: In the MAIA trial, 673 patients with AF/AFL recently converted to sinus rhythm were randomly assigned to receive 50, 100, 200, or 300  mg once‐daily dosing of celivarone; 200  mg daily of amiodarone preceded by a loading dose of 600  mg for 10 days; or placebo. At 3 months’ follow up, no significant difference was observed in time to AF/AFL relapse among the various celivarone groups and placebo. However, fewer symptomatic AF/AFL recurrences were observed in the lower‐dose celivarone groups (26.6% for celivarone 50  mg [P  = 0.022] and 25.2% for celivarone 100  mg [P  = 0.018] vs 40.5% for placebo at 90 days). Fewer adverse events were observed with the use of celivarone and placebo than amiodarone. In the CORYFEE study, 150 patients with AF/AFL were randomly assigned to once‐daily celivarone dosing of 300 or 600  mg, or placebo, for a 2‐day treatment period. There was no significant difference in the rate of spontaneous conversion to sinus rhythm between the treatment and control groups. Conclusions: In these studies, celivarone does not appear to be efficacious in the maintenance of sinus rhythm in AF/AFL patients or for the conversion of AF/AFL patients. (J Cardiovasc Electrophysiol, Vol. 23, pp. 462‐472, May 2012)
Bibliography:ark:/67375/WNG-PD212ZD3-Z
ArticleID:JCE2234
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Dr. Aliot has received consulting fees from Bayer, Biotronik, BMS, Boehringer Ingelheim, GlaxoSmithKline, Meda Pharma, Medtronic, Pfizer, sanofi, and St. Jude Medical, and honoraria from sanofi. Dr. Capucci has received consulting fees from sanofi. Dr. Connolly has received consulting fees and research grants from sanofi. Dr. Crijns has received consulting fees and honoraria/travel reimbursement from sanofi. Dr. Hohnloser has received consulting fees from Boehringer Ingelheim, BMS, Pfizer, and sanofi, and honoraria and lecture fees from BMS, Boehringer Ingelheim, Cardiome, Medtronic, sanofi, and St. Jude Medical. Dr. Kulakowski has received consulting fees and honoraria/travel reimbursement from sanofi. Dr. Roy has received research grants from Cardiome, consulting fees from Daiichi Sankyo, Boehringer Ingelheim, Merck, and sanofi, and lecture fees from sanofi. Dr. Radzik is an employee of sanofi and has equity interest in the company. Dr. Kowey has received consulting and lecture fees from sanofi and honoraria from sanofi. Dr. Khitri made no disclosures.
The MAIA and CORYFEE trials were funded by sanofi‐aventis.
Manuscript received 19 July 2011; Revised manuscript received 11 October 2011; Accepted for publication 25 October 2011.
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ISSN:1045-3873
1540-8167
DOI:10.1111/j.1540-8167.2011.02234.x