Flecainide acetate inhalation solution for cardioversion of recent-onset, symptomatic atrial fibrillation: results of the phase 3 RESTORE-1 trial
Jazyk angličtina Země Velká Británie, Anglie Médium print
Typ dokumentu časopisecké články, randomizované kontrolované studie, multicentrická studie, klinické zkoušky, fáze III
Grantová podpora
InCarda Therapeutics Inc
PubMed
40132102
PubMed Central
PMC11992556
DOI
10.1093/europace/euaf064
PII: 8093443
Knihovny.cz E-zdroje
- Klíčová slova
- Atrial fibrillation, Cardioversion, Flecainide, Oral inhalation,
- MeSH
- antiarytmika * aplikace a dávkování škodlivé účinky MeSH
- aplikace inhalační MeSH
- časové faktory MeSH
- dvojitá slepá metoda MeSH
- elektrokardiografie ambulantní MeSH
- fibrilace síní * farmakoterapie diagnóza patofyziologie MeSH
- flekainid * aplikace a dávkování škodlivé účinky MeSH
- lidé středního věku MeSH
- lidé MeSH
- předčasné ukončení klinických zkoušek MeSH
- senioři MeSH
- srdeční frekvence * účinky léků MeSH
- výsledek terapie MeSH
- Check Tag
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- klinické zkoušky, fáze III MeSH
- multicentrická studie MeSH
- randomizované kontrolované studie MeSH
- Názvy látek
- antiarytmika * MeSH
- flekainid * MeSH
AIMS: Atrial fibrillation (AF) is the most prevalent cardiac arrhythmia. New treatments are needed to cardiovert recent-onset paroxysmal AF quickly and safely. RESTORE-1 was a multicentre, randomized, double-blind, placebo-controlled trial of a 120 mg orally inhaled solution of flecainide acetate (FlecIH-103) for cardioversion of symptomatic, recent-onset (≤48 h) paroxysmal AF. The study aim was to evaluate the efficacy and safety of FlecIH-103 administered via oral inhalation. METHODS AND RESULTS: Patients experiencing a recent-onset paroxysmal AF episode were randomized to receive a single dose of FlecIH-103 or placebo delivered over two 3.5 min inhalation periods, while patients were monitored using 12-lead electrocardiograms and Holter. The trial was stopped prematurely after treating 55 patients, due to lower-than-expected conversion rates and plasma levels. Mean age was 59.6 years, 31.5% of patients were female, and 59.2% were having their first AF episode. Conversion rate was 30.8% (95% confidence interval: 14.7-43.8) for the active group (n = 39) and 0.0% for the placebo group (n = 12) (P = 0.04). Median time to conversion was 12.8 min (IQR: 17.2). In the active group, the mean flecainide plasma level was 198 ng/mL (SD: 156), which is ∼50% lower than in the previous studies. The most common adverse events (AEs) were dysgeusia, dyspnoea, and cough. All AEs were short-lasting and of mild or moderate intensity. CONCLUSION: Despite early termination of the trial, FlecIH-103 was significantly more effective than placebo in cardioverting AF. Safety data did not show any serious AEs. Further studies of FlecIH-103 are needed to optimize the combination of drug formulation and inhalation delivery platform. CLINICAL TRIAL REGISTRATION: URL: https://clinicaltrials.gov, unique identifier: NCT05039359.
Cardiac Arrhythmia Service Massachusetts General Hospital Boston MA USA
Cardiovascular and Genetics Research Institute St George's University of London London UK
Department of Cardiology Deventer Hospital Deventer The Netherlands
Department of Cardiology Diakonessenhuis Utrecht The Netherlands
Department of Cardiology General University Hospital Prague Czechia
Department of Cardiology La Paz University Hospital IdiPaz Universidad Autonoma Madrid Spain
Department of Cardiology Maxima Medical Center Veldhoven The Netherlands
Department of Cardiology Medical Center Leeuwarden Leeuwarden The Netherlands
Department of Cardiology Spaarne Gasthuis Haarlem The Netherlands
Division of Cardiovascular Diseases Lankenau Heart Institute Wynnewood PA USA
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Schnabel RB, Yin X, Gona P, Larson MG, Beiser AS, McManus DD et al. 50 year trends in atrial fibrillation prevalence, incidence, risk factors, and mortality in the Framingham Heart Study: a cohort study. Lancet 2015;386:154–62. PubMed PMC
Iwasaki Y, Nishida K, Kato T, Nattel S. Atrial fibrillation pathophysiology. Circulation 2011;124:2264–74. PubMed
Martín A, Coll-Vinent B, Suero C, Fernández-Simón A, Sánchez J, Varona M et al. Benefits of rhythm control and rate control in recent-onset atrial fibrillation: the HERMES-AF study. Acad Emerg Med 2019;26:1034–43. PubMed
Mohamed MS, Hashem A, Khalouf A, Osama M, Pendela VS, Rai D et al. Delayed vs early cardioversion in patients with paroxysmal atrial fibrillation: a population-based study (2015–2020). Future Cardiol 2023;19:441–52. PubMed
Khan IA. Oral loading single dose flecainide for pharmacological cardioversion of recent-onset atrial fibrillation. Int J Cardiol 2003;87:121–8. PubMed
Crijns HJGM, Van Wijk LM, Van Gilst WH, Kingma JH, Van Gelder IC, Lie KI. Acute conversion of atrial fibrillation to sinus rhythm: clinical efficacy of flecainide acetate. Comparison of two regimens. Eur Heart J 1988;9:634–8. PubMed
Capucci A, Boriani G, Botto GL, Lenzi T, Rubino I, Falcone C et al. Conversion of recent-onset atrial fibrillation by a single oral loading dose of propafenone or flecainide. Am J Cardiol 1994;74:503–5. PubMed
Alp N, Bell J, Shahi M. Randomised double blind trial of oral versus intravenous flecainide for the cardioversion of acute atrial fibrillation. Heart 2000;84:37–40. PubMed PMC
Ibrahim OA, Belley-Côté EP, Um KJ, Baranchuk A, Benz AP, Dalmia S et al. Single-dose oral anti-arrhythmic drugs for cardioversion of recent-onset atrial fibrillation: a systematic review and network meta-analysis of randomized controlled trials. Europace 2021;23:1200–10. PubMed
Markey GC, Salter N, Ryan J. Intravenous flecainide for emergency department management of acute atrial fibrillation. J Emerg Med 2018;54:320–7. PubMed
Verrier RL, Bortolotto AL, Silva BA, Marum AA, Stocco FG, Evaristo E et al. Accelerated conversion of atrial fibrillation to normal sinus rhythm by pulmonary delivery of flecainide acetate in a porcine model. Heart Rhythm 2018;15:1882–8. PubMed
Verrier RL, Belardinelli L. Pulmonary delivery of antiarrhythmic drugs for rapid conversion of new-onset atrial fibrillation. J Cardiovasc Pharmacol 2020;75:276–83. PubMed PMC
Crijns HJGM, Elvan A, Al-Windy N, Tuininga YS, Badings E, Aksoy I et al. Open-label, multicenter study of flecainide acetate oral inhalation solution for acute conversion of recent-onset, symptomatic atrial fibrillation to sinus rhythm. Circ Arrhythm Electrophysiol 2022;15:e010204. PubMed
Ruskin JN, Camm AJ, Dufton C, Woite-Silva AC, Tuininga Y, Badings E et al. Orally inhaled flecainide for conversion of atrial fibrillation to sinus rhythm: INSTANT phase 2 trial. JACC Clin Electrophysiol 2024;10:1021–33. PubMed
Joglar JA, Chung MK, Armbruster AL, Benjamin EJ, Chyou JY, Cronin EM et al. 2023 ACC/AHA/ACCP/HRS guideline for the diagnosis and management of atrial fibrillation: a report of the American College of Cardiology/American Heart Association joint committee on clinical practice guidelines. Circulation 2024;149:e1–156. PubMed PMC
Alboni P, Botto GL, Baldi N, Luzi M, Russo V, Gianfranchi L et al. Outpatient treatment of recent-onset atrial fibrillation with the “pill-in-the-pocket”. Approach. New England Journal of Medicine 2004;351:2384–91. PubMed
Reiffel JA, Blomström-Lundqvist C, Boriani G, Goette A, Kowey PR, Merino JL et al. Real-world utilization of the pill-in-the-pocket method for terminating episodes of atrial fibrillation: data from the multinational antiarrhythmic interventions for managing atrial fibrillation (AIM-AF) survey. Europace 2023;25:euad162. PubMed PMC
Lévy S, Maarek M, Coumel P, Guize L, Lekieffre J, Medvedowsky JL et al. Characterization of different subsets of atrial fibrillation in general practice in France: the ALFA study. The College of French Cardiologists. Circulation 1999;99:3028–35. PubMed
Freeman JV, Simon DN, Go AS, Spertus J, Fonarow GC, Gersh BJ et al. Association between atrial fibrillation symptoms, quality of life, and patient outcomes: results from the outcomes registry for better informed treatment of atrial fibrillation (ORBIT-AF). Circ Cardiovasc Qual Outcomes 2015;8:393–402. PubMed
National Library of Medicine; National Institutes of Health; U.S. Department of Health and Human Services. FLECAINIDE ACETATE tablet . Package Insert [Internet]. Aurobindo Pharma Limited. 2020. https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=14e89448-3a18-42e3-8537-2589be1ef94e (cited 11 February 2023)
Suttorp MJ, Kingma JH, Jessurun ER, Lie-A-Huen L, van Hemel NM, Lie KI. The value of class IC antiarrhythmic drugs for acute conversion of paroxysmal atrial fibrillation or flutter to sinus rhythm. J Am Coll Cardiol 1990;16:1722–7. PubMed
Roy D, Pratt CM, Torp-Pedersen C, Wyse DG, Toft E, Juul-Moller S et al. Vernakalant hydrochloride for rapid conversion of atrial fibrillation: a phase 3, randomized, placebo-controlled trial. Circulation 2008;117:1518–25. PubMed
Roy D, Rowe BH, Stiell IG, Coutu B, Ip JH, Phaneuf D et al. A randomized, controlled trial of RSD1235, a novel anti-arrhythmic agent, in the treatment of recent onset atrial fibrillation. J Am Coll Cardiol 2004;44:2355–61. PubMed
ClinicalTrials.gov
NCT05039359