US2021069158A1PendingUtilityA1

Methods of Preventing Occurrence of Cardiovascular Events

70
Assignee: KOWA COPriority: Jul 29, 2016Filed: Nov 16, 2020Published: Mar 11, 2021
Est. expiryJul 29, 2036(~10.1 yrs left)· nominal 20-yr term from priority
A61P 9/04A61P 3/10A61K 31/423A61K 31/366A61K 31/40A61K 9/0053A61K 45/06A61K 31/41A61K 31/505A61P 9/00A61K 31/47
70
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Claims

Abstract

The present invention relates to pharmacological interventions with pemafibrate for cardiovascular diseases and adverse cardiovascular events. In addition, the invention relates to the use of pemafibrate to treat dyslipidemia and type 2 diabetes mellitus and thereby reduce the risk of cardiovascular disease and adverse cardiovascular events.

Claims

exact text as granted — not AI-modified
1 - 29 . (canceled) 
     
     
         30 . A method of treating a patient having one or more risk factors for cardiovascular events to reduce the risk of a cardiovascular event, wherein the patient is on concomitant lipid-lowering therapy other than concomitant moderate to high intensity statin therapy and has an LDL-C concentration<70 mg/dL, comprising administering to the patient a therapeutically effective amount of pemafibrate or a pharmaceutically acceptable salt thereof. 
     
     
         31 . The method of  claim 30 , wherein the patient has type 2 diabetes mellitus. 
     
     
         32 . The method of  claim 30 , wherein the patient has an age greater than or equal to 50 years if male or 55 years if female, or has atherosclerosis. 
     
     
         33 . The method of  claim 30 , wherein the patient is taking a concurrent statin. 
     
     
         34 . The method of  claim 30 , wherein the patient has a fasting TG concentration>200 mg/dL and <500 mg/dL. 
     
     
         35 . The method of  claim 30 , wherein the patient has an HDL-C concentration<40 mg/dL. 
     
     
         36 . The method of  claim 30 , wherein the patient has:
 a) type 2 diabetes mellitus;   b) a fasting TG concentration>200 mg/dL and <500 mg/dL; and   c) an HDL-C concentration<40 mg/dL.   
     
     
         37 . The method of  claim 30 , wherein the patient is taking a concurrent statin and has:
 a) type 2 diabetes mellitus;   b) a fasting TG concentration>200 mg/dL and <500 mg/dL; and   c) an HDL-C concentration>35 mg/dL and <40 mg/dL.   
     
     
         38 . The method of  claim 36  wherein:
 a) the patient has an age greater than or equal to 50 years if male or 55 years if female, or atherosclerosis; and 
 b) the therapeutically effective amount of pemafibrate or pharmaceutically acceptable salt thereof is 0.4 mg, administered orally per day. 
 
     
     
         39 . The method of  claim 30 , wherein the therapeutically effective amount of pemafibrate or pharmaceutically acceptable salt thereof is from 0.2 to 1.0 mg, administered orally per day. 
     
     
         40 . The method of  claim 30 , wherein the therapeutically effective amount of pemafibrate or pharmaceutically acceptable salt thereof is 0.4 mg, administered orally per day. 
     
     
         41 . The method of  claim 30 , wherein the therapeutically effective amount of pemafibrate or a pharmaceutically acceptable salt thereof is 0.2 mg, administered orally twice daily. 
     
     
         42 . The method of  claim 30 , wherein the cardiovascular events are selected from nonfatal myocardial infarction, nonfatal ischemic stroke, hospitalization for unstable angina requiring unplanned coronary revascularization, cardiovascular death, and combinations thereof. 
     
     
         43 . The method of  claim 30 , wherein the patient has type 2 diabetes mellitus as defined by:
 a) a hemoglobin A1c level of 6.5% or greater; and   b) a plasma glucose level:
 i) greater than or equal to 126 mg/dL when fasting; 
 ii) greater than or equal to 200 mg/dL at 2 hours during oral glucose tolerance testing; or 
 iii) greater than or equal to 200 mg/dL with classic type 2 diabetes mellitus symptoms. 
   
     
     
         44 . A method of reducing the risk of the occurrence of a cardiovascular event in a patient with one or more risk factors, wherein the patient has an LDL-C concentration<70 mg/dL, comprising administering to the patient a therapeutically effective amount of pemafibrate or a pharmaceutically acceptable salt thereof. 
     
     
         45 . The method of  claim 44 , wherein the patient is taking a concurrent statin. 
     
     
         46 . The method of  claim 44 , wherein the patient has a fasting TG concentration>200 mg/dL and <500 mg/dL. 
     
     
         47 . The method of  claim 44 , wherein the patient is a male with has an HDL-C concentration>35 mg/dL and <40 mg/dL. 
     
     
         48 . The method of  claim 44 , wherein the patient has:
 a) type 2 diabetes mellitus;   b) a fasting TG concentration>200 mg/dL and <500 mg/dL; and   c) an HDL-C concentration<40 mg/dL.   
     
     
         49 . The method of  claim 44 , wherein the cardiovascular events are selected from nonfatal myocardial infarction, nonfatal ischemic stroke, hospitalization for unstable angina, cardiovascular death, and combinations thereof.

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