IP Library Granted Patent US 11,141,399
Granted Patent B2
US 11,141,399 · App. 17/106,741 · Granted Oct 12, 2021

Methods of treating or preventing nonalcoholic steatohepatitis and/or primary biliary cirrhosis

Inventors: Mehar Manku (Birmingham, GB); Pierre Wicker (Mystic, CT); Rene Braeckman (Richboro, PA); Paresh Soni (Mystic, CT); Joseph S. Zakrzewski (Bedminster, NJ)
Assignee: Amarin Pharmaceuticals Ireland Limited
A61K31/232A61K9/4808A61K9/4825A61K31/05A61K31/07A61K31/198A61K31/202A61K31/557A61K31/575A61K33/04A61K45/06
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Quick Facts
Patent No.
US 11,141,399
App. No.
17/106,741
Granted
Oct 12, 2021
Kind
B2
Abstract

In various embodiments, the present invention provides methods of treating and/or preventing NASH and/or PBC comprising administering to a subject in need thereof a pharmaceutical composition comprising eicosapentaenoic acid or a derivative thereof.

Claims (11)

1. A method of inhibiting Farnesoid X receptors (“FXR”) in a subject having triglyceride levels of at least about 500 mg/dL, the method comprising administering orally to the subject about 4 g of ethyl eicosapentaenoate per day.

2. The method of claim 1 , wherein the method comprises administering orally to the subject about 4 capsules per day, each capsule comprising about 900 mg to about 1.1 g of ethyl eicosapentaenoate and not more than about 20%, by weight, of total fatty acids present in the capsule, docosahexaenoic acid or its esters.

3. The method of claim 1 , wherein prior to administration of ethyl eicosapentaenoate, the subject has one or more of: an elevated baseline alanine aminotransferase (“ALT”) level, an elevated baseline aspartate aminotransferase (“AST”) level, liver fibrosis, an elevated baseline gamma-glutamyl transferase level, an elevated baseline alkaline phosphatase level, an elevated baseline antimitochondrial antibody level, an elevated baseline antinuclear antibody level, an elevated total serum bilirubin level, and/or an elevated transaminase level.

4. The method of claim 1 , wherein after administration of the ethyl eicosapentaenoate, the subject has one or more of: a reduced ALT level, a reduced AST level, reduced liver fibrosis, a reduced gamma-glutamyl transferase level, a reduced alkaline phosphatase level, a reduced antimitochondrial antibody level, a reduced antinuclear antibody level, a reduced total serum bilirubin level, and a reduced transaminase level.

5. The method of claim 4 , wherein a triglyceride level, an IgM level, and/or a C-reactive protein level is reduced in the subject.

6. The method of claim 5 , wherein the subject exhibits one or more of: a reduction in an IgM level of at least about 0.5 g/L and a reduction in C-reactive protein level of at least about 30%.

7. The method of claim 1 , wherein the ethyl eicosapentaenoate is present in a composition and represents at least about 90%, by weight, of total fatty acids present in the composition.

8. The method of claim 7 , wherein the ethyl eicosapentaenoate represents at least about 96%, by weight, of total fatty acids present in the composition.

9. The method of claim 7 , wherein the composition comprises less than about 10%, by weight, of total fatty acids present in the composition, docosahexaenoic acid or its esters.

10. The method of claim 9 , wherein the composition comprises less than about 3%, by weight, of total fatty acids present in the composition, docosahexaenoic acid or its esters.

11. The method of claim 10 , wherein the composition comprises substantially no docosahexaenoic acid or its esters.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 29, 2021
From: MANKU, MEHAR; OSTERLOH, IAN; WICKER, PIERRE; BRAECKMAN, RENE; SONI, PARESH; ZAKRZEWSKI, JOE
To: AMARIN PHARMACEUTICALS IRELAND LIMITED
Reel/Frame 055186/0552 →