US2022071951A1PendingUtilityA1
Therapeutic agent for inherited bradyarrhythmia
Est. expiryDec 28, 2038(~12.4 yrs left)· nominal 20-yr term from priority
A61K 31/4741A61P 9/06A61K 31/353
64
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Claims
Abstract
A therapeutic agent for bradyarrythmia contains the following compound (I) or compound (II) or a pharmacologically acceptable salt thereof as an active component:(wherein, Ph is a phenyl group).
Claims
exact text as granted — not AI-modified1 . A therapeutic agent for bradyarrythmia containing the following compound (I) or compound (II) or a pharmacologically acceptable salt thereof as an active component:
(wherein, Ph is a phenyl group).
2 . The therapeutic agent according to claim 1 , wherein
the bradyarrythmia is inherited bradyarrythmia.
3 . The therapeutic agent according to claim 1 , wherein
the bradyarrythmia is any of sinus bradycardia, sinus arrest, sinoatrial block and atrioventricular block.
4 . The therapeutic agent according to claim 1 , wherein
the bradyarrythmia is any of sinus bradycardia, sinus arrest, sinoatrial block and atrioventricular block and is inherited bradyarrythmia.
5 . The therapeutic agent according to claim 1 , containing the following compound (I) or a pharmacologically acceptable salt thereof as an active component:
(wherein, Ph is a phenyl group).
6 . The therapeutic agent according to claim 1 , containing the following compound (II) or a pharmacologically acceptable salt thereof as an active component:
(wherein, Ph is a phenyl group).
7 . The therapeutic agent according to claim 1 , wherein
the bradyarrythmia is an arrhythmia caused by a mutation in the 83rd amino acid from the N-terminus of a KCNJ3 protein from asparagine (N) to histidine (H).
8 . The therapeutic agent according to claim 1 , wherein
the bradyarrythmia is an arrhythmia caused by a mutation in the 101st amino acid from the N-terminus of a KCNJ5 protein from tryptophan (W) to cysteine (C).Join the waitlist — get patent alerts
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