US2022249409A1PendingUtilityA1
Early administration of low-dose colchicine after myocardial infarction
Assignee: INST DE CARDIOLOGIE DE MONTREALPriority: Nov 15, 2019Filed: Apr 27, 2022Published: Aug 11, 2022
Est. expiryNov 15, 2039(~13.3 yrs left)· nominal 20-yr term from priority
Inventors:Jean-Claude Tardif
A61P 9/10A61K 31/165
68
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Claims
Abstract
The invention relates to colchicine for use in a method of treating a patient after having a myocardial infarction (MI), the method including initiating the administration of colchicine at a daily low dose to the patient within about 3 days of the MI.
Claims
exact text as granted — not AI-modifiedWhat is claimed is:
1 . A method of treating a patient after having a myocardial infarction (MI), the method comprising initiating the administration of colchicine at a daily low dose to the patient within about 3 days of the MI.
2 . The method according to claim 1 , wherein percutaneous coronary intervention was performed for treating the patient's MI.
3 . The method according to claim 1 , wherein the patient was prescribed a medication.
4 . The method according to claim 3 , wherein the medication is an antiplatelet agent.
5 . The method according to claim 3 , wherein the medication is aspirin.
6 . The method according to claim 3 , wherein the medication is a statin.
7 . The method according to claim 1 , wherein the patient is at a lower risk of a cardiovascular event, relative to a patient not being administered colchicine.
8 . The method according to claim 7 , wherein the cardiovascular event is an ischemic cardiovascular event.
9 . The method according to claim 7 , wherein the cardiovascular event is resuscitated cardiac arrest.
10 . The method according to claim 7 , wherein the cardiovascular event is myocardial infarction.
11 . The method according to claim 7 , wherein the cardiovascular event is stroke.
12 . The method according to claim 7 , wherein the cardiovascular event is urgent hospitalization for angina requiring coronary revascularization.
13 . The method according to claim 1 , wherein the patient has atherosclerotic coronary artery disease.
14 . The method according to claim 1 , wherein the administration of colchicine is initiated upon assessment in (a) an emergency department (ED), (b) the hospital, or (c) a medical office setting.
15 . The method according to claim 1 , wherein the colchicine is in the form of a tablet.
16 . The method of claim 15 , wherein the tablet is coated.
17 . The method of claim 16 , wherein the tablet is film-coated.
18 . The method according to claim 1 , wherein the colchicine is administered at 0.3 to 0.7 mg.
19 . The method according to claim 18 , wherein the colchicine is administered at 0.4 to 0.6 mg
20 . The method according to claim 16 , wherein the colchicine is administered at 0.5 mg.
21 . The method according to claim 9 , wherein the colchicine is administered at 0.5 mg.
22 . The method according to claim 10 , wherein the colchicine is administered at 0.5 mg.
23 . The method according to claim 11 , wherein the colchicine is administered at 0.5 mg.
24 . The method according to claim 12 , wherein the colchicine is administered at 0.5 mg.
25 . The method according to claim 1 , wherein the colchicine is administered once, twice or three times a day.
26 . The method according to claim 25 , wherein the colchicine is administered once per day.
27 . The method according to claim 1 , wherein the colchicine is administered without pre-loading the patient with colchicine.
28 . The method according to claim 1 , wherein the patient is an adult human.
29 . A method of reducing the risk of a stroke in a patient after having an MI, the method comprising initiating the administration of colchicine at a daily low dose to the patient within about 30 days of an MI.
30 . The method according to claim 29 , wherein the method comprises administering colchicine within 4 to 7 days of the MI.Join the waitlist — get patent alerts
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