IP Library Granted Patent US 11,969,422
Granted Patent B2
US 11,969,422 · App. 17/540,638 · Granted Apr 30, 2024

Methods of treating heart failure with reduced ejection fraction using modified forms of trimetazidine

Inventors: Jaikrishna Patel (Cary, NC); Paul Chamberlin (Brookline, MA)
Assignee: IMBRIA PHARMACEUTICALS, INC.
A61K31/496A61K9/0053A61P9/04
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 11,969,422
App. No.
17/540,638
Granted
Apr 30, 2024
Kind
B2
Abstract

The invention provides methods of treatment of heart failure with reduced ejection fraction (HFrEF) using modified forms of trimetazidine, such as CV-8972 and CV-8814.

Claims (20)

1. A method of treating heart failure associated with reduced ejection fraction (HFrEF) in a subject, the method comprising providing to a subject having HFrEF a compound represented by formula (X):

or a pharmaceutically acceptable salt thereof.

2. The method of claim 1 , wherein the HFrEF is associated with a condition selected from the group consisting of aortic stenosis, arrhythmia, cerebrovascular accident, chronic obstructive pulmonary disease, cigarette smoking, congenital heart disease, diabetic cardiomyopathy, dilated cardiomyopathy, hypertension, ischemic coronary disease, kidney disease, low baseline left ventricular ejection fraction, low platelet count, male gender, mitral regurgitation, myocardial infarction, myocarditis, obstructive hypertrophic cardiomyopathy, obesity, old age, peripheral vascular disease, renal disease, rheumatic heart disease, valvular disease, and viral myocarditis.

3. The method of claim 1 , wherein the compound is provided in a pharmaceutical composition.

4. The method of claim 3 , wherein the pharmaceutical composition is provided orally.

5. The method of claim 4 , wherein the composition comprises a format selected from the group consisting of a tablet, troche, lozenge, aqueous suspension, oily suspension, emulsion, hard capsule, soft capsule, and syrup.

6. The method of claim 3 , wherein the pharmaceutical composition comprises a mixture of the compound and an erodible polymer that promotes swelling of the mixture in an aqueous environment.

7. The method of claim 6 , wherein the erodible polymer is hydroxypropyl methylcellulose (HPMC).

8. The method of claim 7 , wherein the mixture comprises the compound and HMPC in a ratio of from about 1:10 to about 10:1.

9. The method of claim 3 , wherein the pharmaceutical composition is a unit dosage comprising from about 10 mg to about 500 mg of the compound.

10. A method of treating heart failure associated with reduced ejection fraction (HFrEF) in a subject, the method comprising providing to a subject having HFrEF a compound represented by formula (IX):

or a pharmaceutically acceptable salt thereof.

11. The method of claim 10 , wherein the HFrEF is associated with a condition selected from the group consisting of aortic stenosis, arrhythmia, cerebrovascular accident, chronic obstructive pulmonary disease, cigarette smoking, congenital heart disease, diabetic cardiomyopathy, dilated cardiomyopathy, hypertension, ischemic coronary disease, kidney disease, low baseline left ventricular ejection fraction, low platelet count, male gender, mitral regurgitation, myocardial infarction, myocarditis, obstructive hypertrophic cardiomyopathy, obesity, old age, peripheral vascular disease, renal disease, rheumatic heart disease, valvular disease, and viral myocarditis.

12. The method of claim 10 , wherein the compound is provided in a pharmaceutical composition.

13. The method of claim 12 , wherein the pharmaceutical composition is provided orally.

14. The method of claim 13 , wherein the composition comprises a format selected from the group consisting of a tablet, troche, lozenge, aqueous suspension, oily suspension, emulsion, hard capsule, soft capsule, and syrup.

15. The method of claim 12 , wherein the pharmaceutical composition comprises a mixture of the compound and an erodible polymer that promotes swelling of the mixture in an aqueous environment.

16. The method of claim 15 , wherein the erodible polymer is hydroxypropyl methylcellulose (HPMC).

17. The method of claim 16 , wherein the mixture comprises the compound and HMPC in a ratio of from about 1:10 to about 10:1.

18. The method of claim 12 , wherein the pharmaceutical composition is a unit dosage comprising from about 10 mg to about 500 mg of the compound.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 12, 2022
From: PATEL, JAIKRISHNA; CHAMBERLIN, PAUL
To: IMBRIA PHARMACEUTICALS, INC.
Reel/Frame 058631/0958 →
Continuity (2)
Provisional Application 63123728 · Dec 10, 2020
Related Publication 20220184062A1 · Jun 16, 2022
Cited By (2)
US 12,318,453 US 12,649,720