US2015224076A1PendingUtilityA1
Compositions comprising 15-ohepa and methods of using the same
Est. expiryJan 30, 2033(~6.6 yrs left)· nominal 20-yr term from priority
A61P 1/00A61P 1/16A61K 31/557A61K 9/0053A61K 31/202A61K 9/48A61K 31/232
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Claims
Abstract
The present invention relates to the compositions, formulations and methods of treating fatty liver disorders, such as non-alcoholic fatty liver disease (NAFLD) and non-alcoholic steatohepatitis (NASH) and their sequelae by administration of 15-OHEPA.
Claims
exact text as granted — not AI-modified1 . A method for treating or preventing liver disease in a subject comprising, administering to the subject 15-HEPE in an amount effective to treat or prevent liver disease in the subject.
2 . The method of claim 1 wherein the 15-HEPE is present in a pharmaceutical composition.
3 . The method of claim 1 , wherein the liver disease is non-alcoholic steatohepatitis.
4 . The method of claim 2 , wherein the 15-HEPE is present in the pharmaceutical composition in an amount from about 1 mg to about 1000 mg.
5 . The method of claim 2 , wherein the 15-HEPE represents at least about 1% to about 95% of all fatty acids present in the pharmaceutical composition.
6 . The method of claim 2 , wherein the 15-HEPE represents at least about 60%, by weight, of all fatty acids present in the pharmaceutical composition.
7 . The method of claim 2 , wherein the 15-HEPE represents at least about 70%, by weight, of all fatty acids present in the pharmaceutical composition.
8 . The method of claim 2 , wherein the 15-HEPE represents at least about 90%, by weight, of all fatty acids present in the pharmaceutical composition.
9 . The method of claim 2 , wherein the 15-HEPE represents substantially all fatty acids present in the pharmaceutical composition.
10 . The method of claim 2 , wherein the 15-HEPE represents all fatty acids present in the pharmaceutical composition.
11 . The method of claim 2 wherein the composition is free of any other omega-3 fatty acids.
12 . The method of claim 2 , wherein the administering step includes administering the pharmaceutical composition to the subject about 1 to about 4 times per day.
13 . The method of claim 2 , wherein the pharmaceutical composition is present in one or more dosage units.
14 . The method of claim 13 , wherein the one or more dosage units comprise orally deliverable capsules.
15 . The method of claim 1 , wherein the subject has a predisposition to and/or a diagnosis of the liver disease.
16 . The method of claim 1 , wherein the liver disease is non-alcoholic fatty liver disease (NAFLD).
17 . The method of claim 2 , wherein the pharmaceutical composition comprises about 0.1% to about 99%, by weight, 15-HEPE.
18 . The method of claim 2 , wherein the pharmaceutical composition comprises at least about 50%, by weight, 15-HEPE.Cited by (0)
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