US2019076417A1PendingUtilityA1

Compositions and methods for treating or preventing atrial fibrillation

Assignee: UNIV NORTHWESTERNPriority: May 12, 2010Filed: Apr 2, 2018Published: Mar 14, 2019
Est. expiryMay 12, 2030(~3.8 yrs left)· nominal 20-yr term from priority
A61K 31/47A61K 31/18A61K 31/4725A61K 31/135A61K 31/5377A61K 31/215A61K 31/46A61K 31/522A61K 31/4025A61K 31/4545A61K 31/165A61K 31/437A61K 31/551A61K 31/44A61K 31/138A61P 9/04A61K 31/22A61K 31/137A61K 31/24A61K 31/445A61P 9/06A61K 31/132A61K 31/404A61K 2300/00A61K 31/352
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Claims

Abstract

The present invention provides compositions and methods for treating or preventing atrial fibrillation (AF). In particular, the present invention provides administration of muscarinic receptor antagonists (e.g., M2-selective muscarinic receptor blockers), administered alone or in combination with other therapeutic agents (e.g., beta-adrenergic receptor blockers) to treat and/or prevent atrial fibrillation.

Claims

exact text as granted — not AI-modified
1 . A method of treating, reversing, and/or preventing cardiac arrhythmia in a subject comprising co-administering to said subject a therapeutically effective amount of a beta-adrenergic receptor blocking agent and a therapeutically effective amount of a muscarinic receptor blocking agent. 
     
     
         2 . The method of  claim 1 , wherein said beta-adrenergic receptor blocking agent is selected from the group consisting of aprenolol, carteolol, levobunolol, mepindolol, metipranolol, nadolol, oxprenolol, timolol, sotalol, esmolol, cateolol, propranolol, betaxolol, penbutolol, metoprolol, acebutolol, atenolol, metoprolol, pindolol, bisoprolol, nebivolol, amosulalol, landiolol, and tilisolol, including any salts, hydrates, solvates, prodrugs, and any crystal forms in which they may occur. 
     
     
         3 . The method of  claim 1 , wherein said muscarinic receptor blocker is selected from the group comprising atropine, scopolamine, ipratropium, tropicamide, pirenzepine, diphenhydramine, dimenhydrinate, dicyclomine, oxybutynin, tiotropium, cyclopentolate, atropine methonitrate, trihexyphenidyl, tolterodine, solifenacin, darifenacin, benzatropine, and mebeverine, including any salts, hydrates, solvates, prodrugs, and any crystal forms in which they may occur. 
     
     
         4 . The method of  claim 1 , wherein said muscarinic receptor blocker is a M 2 -selective muscarinic receptor subtype. 
     
     
         5 . The method of  claim 1 , wherein said cardiac arrhythmia comprises atrial fibrillation. 
     
     
         6 . The method of  claim 1 , wherein said co-administering of said beta-adrenergic blocker and said muscarinic receptor blocker comprises applying directly to the surface of the heart. 
     
     
         7 - 12 . (canceled) 
     
     
         13 . A method of treating, reversing, and/or preventing cardiac arrhythmia in a subject comprising administering to said subject a therapeutically effective amount of an M 2 -selective muscarinic receptor blocking agent. 
     
     
         14 . The method of  claim 13 , wherein the cardiac arrhythmia is atrial fibrillation. 
     
     
         15 . The method of  claim 13 , wherein said M 2 -selective muscarinic receptor blocking agent selectively blocks the M 2  receptor subtype by at least five-fold versus the M 3  receptor subtype. 
     
     
         16 . The method of  claim 15 , wherein said M 2 -selective muscarinic receptor blocking agent selectively blocks the M 2  receptor subtype by at least five-fold versus the M 1  receptor subtype. 
     
     
         17 . The method of  claim 1 , wherein said M 2 -selective muscarinic receptor blocking agent is selected from Sch 211803, TD-6301, and methoctramine. 
     
     
         18 . A method of treating cardiac arrhythmias comprising:
 (a) testing a subject to determine the presence, type, and/or severity of a cardiac arrhythmia;   (b) administering to said subject a therapeutically effective amount of a M 2 -selective muscarinic receptor blocking agent; and   (c) evaluating said subject for a change in said cardiac arrhythmia.   
     
     
         19 - 20 . (canceled) 
     
     
         21 . The method of  claim 1 , wherein the muscarinic receptor blocker is atropine and is administered at a dose of 0.8 mg/kg.

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