US2020000870A1PendingUtilityA1
Methods for treatment of atherosclerosis
Est. expiryAug 2, 2032(~6.1 yrs left)· nominal 20-yr term from priority
A61K 45/06A61K 38/07A61K 31/366A61K 31/22A61K 31/40A61K 31/505A61P 9/10A61K 31/404A61K 31/215A61K 31/351
71
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Claims
Abstract
Disclosed herein are methods and compositions for preventing or treating atherosclerosis in a mammalian subject. The methods comprise administering to the subject an effective amount of an aromatic-cationic peptide and, in some applications, a second active agent, to subjects in need thereof. The present technology relates to the treatment or prevention of atherosclerosis in mammals through the administration of a therapeutically effective amount of aromatic cationic peptides and, in some embodiments, a second active agent.
Claims
exact text as granted — not AI-modified1 .- 30 . (canceled)
31 . A method for delaying onset, ameliorating or eliminating statin side effects in a subject in need thereof, the method comprising administering simultaneously, separately or sequentially with the statin, an effective amount of a peptide D-Arg-2′6′-Dmt-Lys-Phe-NH 2 or a pharmaceutically acceptable salt thereof, wherein the statin side effect comprises mitochondrial dysfunction.
32 . The method of claim 31 , wherein the statin is selected from the group consisting of: atorvastatin, simvastatin, pravastatin, fluvastatin, lovastatin, pitavastatin, rosuvastatin, niacin extended-release/lovastatin, lovastatin extended-release, amlodipine, atorvastatin, rosuvastatin, sitagliptin/simvastatin, fluvastatin, fluvastatin extended-release, atorvastatin, pitavastatin, lovastatin, pravastatin, niacin extended-release/simvastatin, ezetimibe/simvastatin, and simvastatin.
33 . The method of claim 31 , wherein the peptide and statin are administered sequentially in either order.
34 . The method of claim 31 , wherein the pharmaceutically acceptable salt comprises acetate salt or trifluoroacetate salt.
35 . The method of claim 31 , wherein the statin comprises rosuvastatin or atorvastatin.Cited by (0)
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