US2021338617A1PendingUtilityA1
Compositions and Methods for Treating Chronic Inflammation and Inflammatory Diseases
Est. expiryOct 29, 2030(~4.3 yrs left)· nominal 20-yr term from priority
Inventors:Robin M. BannisterJohn BrewWilson Romero Caparros-WanderleyGregory Alan StoloffSuzanne Jane DillyGemma SzucsOlga Pleguezuelos Mateo
A61K 31/192A61P 7/02A61K 9/08A61K 31/22A61P 1/00A61P 9/12A61K 31/216A61P 1/18A61P 15/02A61P 17/00A61P 31/00A61P 35/00A61K 31/60A61P 25/06A61P 9/00A61K 31/196A61K 31/19A61K 31/40A61P 11/06A61P 19/02A61P 17/10A61P 3/10A61P 3/04A61P 37/00A61P 3/06A61K 47/44A61P 1/16A61P 19/10A61K 47/10A61P 29/00A61K 9/2013A61P 37/06A61P 1/02A61P 25/28A61K 47/14A61K 31/215A61P 9/04A61P 25/00Y02A50/30A61K 47/34A61P 13/12A61P 11/02A61P 17/02A61P 37/08A61P 7/06A61P 9/10A61P 27/02A61P 11/00A61P 25/16
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Claims
Abstract
The present specification discloses pharmaceutical compositions, methods of preparing such pharmaceutical compositions, and methods and uses of treating a chronic inflammation and/or an inflammatory disease in an individual using such pharmaceutical compositions.
Claims
exact text as granted — not AI-modified1 . A pharmaceutical composition formulated as a suspension for oral administration, the suspension comprising solid particles of an asprin in an oil carrier,
the asprin solid particles in an amount of at least 20% by weight of the pharmaceutical composition, the oil carrier in an amount of at least 10% by weight of the pharmaceutical composition, and the oil carrier comprising (i) at least 80% of one or more free fatty acids, each of the one or more free fatty acids having at least 8 carbon atoms and being a liquid at room temperature and (ii) a phospholipid.
2 . The pharmaceutical composition of claim 1 , wherein the asprin solid particles are in an amount of about 25% to about 50% by weight of the pharmaceutical composition.
3 . The pharmaceutical composition of claim 1 , wherein the oil carrier is in an amount of at least 40% by weight of the pharmaceutical composition.
4 . The pharmaceutical composition of claim 3 , wherein the oil carrier is in an amount of at least 45% by weight of the pharmaceutical composition.
5 . The pharmaceutical composition of claim 4 , wherein the oil carrier is in an amount of at least 50% by weight of the pharmaceutical composition.
6 . The pharmaceutical composition of claim 1 , wherein the one or more free fatty acids are in an amount of at least 85% by weight of the pharmaceutical composition.
7 . The pharmaceutical composition of claim 1 , wherein the one or more free fatty acids are in an amount of at least 90% by weight of the pharmaceutical composition.
8 . The pharmaceutical composition of claim 1 , wherein the one or more free fatty acids are in an amount of at least 95% by weight of the pharmaceutical composition.
9 . The pharmaceutical composition of claim 1 , wherein the one or more free fatty acids includes a saturated free fatty acid, an unsaturated free fatty acid, or both saturated and unsaturated free fatty acids.
10 . The pharmaceutical composition of claim 1 , wherein the oil carrier comprises one free fatty acid having at least 8 carbon atoms.
11 . The pharmaceutical composition of claim 10 , wherein the one free fatty acid is an oleic acid.
12 . The pharmaceutical composition of claim 1 , wherein the oil carrier comprises a plurality of different free fatty acids, each of the plurality of different free fatty acids having at least 8 carbon atoms.
13 . The pharmaceutical composition of claim 12 , wherein the plurality of different free fatty acids includes a palmitic acid, a stearic acid, an oleic acid, a linoleic acid, a linolenic acid, or any combination thereof.
14 . The pharmaceutical composition of claim 1 , wherein the free fatty acid is a lauric acid, a tridecylic acid, a myristic acid, a myristoleic acid, a pentadecyclic acid, a palmitic acid, a palmitoleic acid, a sapienic acid, a margaric acid, a stearic acid, an oleic acid, an elaidic acid, a vaccenic acid, a linoleic acid, a linoelaidic acid, an α-Linolenic acid, a γ-Linolenic acid, a stearidonic acid, a nonadecylic acid, an arachidic acid, an eicosenoic acid, a dihomo-γ-linolenic acid, a mead acid, an arachidonic acid, an eicosapentaenoic acid, a heneicosylic acid, a behenic acid, an erucic acid, a docosahexaenoic acid, a tricosylic acid, a lignoceric acid, a nervonic acid, or any combination thereof.
15 . The pharmaceutical composition of claim 1 , wherein the phospholipid is a zwitterionic phospholipid.
16 . The pharmaceutical composition of claim 1 , wherein the phospholipid includes a phosphodiacylglyceride or a phosphosphingolipid.
17 . The pharmaceutical composition of claim 1 , wherein the phospholipid is a phosphatidylcholine, a phosphatidylserine, a phosphatidylethanolamine, a phosphatidylinositol, a sphingomyelin, or any combination thereof.
18 . The pharmaceutical composition of claim 1 , wherein the pharmaceutical composition is formulated in the absence of a solvent.
19 . A pharmaceutical composition formulated as a suspension for oral administration, the suspension comprising solid particles of an asprin in an oil carrier,
the oil carrier being in an amount of at least 40% by weight of the pharmaceutical composition, and the oil carrier comprising (i) at least 90% of one or more free fatty acids, each of the one or more free fatty acids having at least 8 carbon atoms and being a liquid at room temperature and (ii) a phospholipid.
20 . The pharmaceutical composition of claim 19 , wherein the phospholipid is a zwitterionic phospholipid.Join the waitlist — get patent alerts
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