US2016220524A1PendingUtilityA1
Compositions of small molecule therapeutics
Est. expiryMay 4, 2030(~3.8 yrs left)· nominal 20-yr term from priority
A61K 9/0095A61K 31/655A61K 31/635A61K 47/18A61K 47/14A61K 31/7008A61K 31/451A61K 31/549A61K 31/138A61K 31/165A61K 9/4858A61K 31/4515A61K 9/0019A61K 31/4439A61K 31/445A61K 31/221A61K 31/337A61P 35/00A61K 47/10A61K 31/341A61K 31/335
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Claims
Abstract
Compositions containing a small molecule therapeutic and an alkyl N,N-disubstituted amino acetate are disclosed. Inclusion of the alkyl N,N-disubstituted amino acetate enhances the pharmacokinetic properties of the small molecule therapeutic.
Claims
exact text as granted — not AI-modified1 - 30 . (canceled)
31 . An oral or subcutaneously injectable composition comprising a small molecule therapeutic, an alkyl N,N-disubstituted-amino acetate, and one or more pharmaceutically acceptable carriers.
32 . The composition in accordance with claim 31 wherein the small molecule therapeutic is selected from the group consisting of a taxane, and a compound classified under the Biopharmaceutics Classification System (BCS) in at least one of Class 2, Class 3 or Class 4.
33 . The composition in accordance with claim 32 wherein the taxane is a member of the group consisting of paclitaxel, docetaxel, tesetaxel, and mixtures thereof.
34 . The composition in accordance with claim 32 wherein the compound is a member of BCS Class 2.
35 . The composition in accordance with claim 34 wherein the compound is selected from the group consisting of lansoprazole, haloperidol, sulfasalazine, and glibenclamide.
36 . The composition in accordance with claim 32 wherein the compound is a member of BCS Class 3.
37 . The composition in accordance with claim 36 wherein the compound is selected from the group consisting of atenolol, glucosamine or salt thereof, and cimetidine.
38 . The composition in accordance with claim 32 wherein the compound is a member of BCS Class 4.
39 . The composition in accordance with claim 38 wherein the compound is selected from the group consisting of furosemide, chlorothiazide, and hydrochlorothiazide.
40 . The composition in accordance with claim 31 wherein the alkyl N,N-disubstituted-amino acetate is dodecyl 2-(N,N-dimethylamino) propionate.
41 . The composition in accordance with claim 31 wherein the alkyl N,N-disubstituted-amino acetate is dodecyl 2-(N,N-dimethylamino) propionate hydrochloride.
42 . The composition in accordance with claim 31 wherein the small molecule therapeutic is a taxane and the alkyl N,N-disubstituted amino acetate is dodecyl 2-(N,N-dimethylamino) propionate.
43 . The composition in accordance with claim 31 wherein the small molecule therapeutic is a taxane and the alkyl N,N-disubstituted amino acetate is dodecyl 2-(N,N-dimethylamino) propionate hydrochloride.
44 . The composition in accordance with claim 31 wherein the small molecule therapeutic is paclitaxel and the alkyl N,N-disubstituted amino acetate is dodecyl 2-(N,N-dimethylamino) propionate.
45 . The composition in accordance with claim 31 wherein the small molecule therapeutic is a paclitaxel and the alkyl N,N-disubstituted amino acetate is dodecyl 2-(N,N-dimethylamino) propionate hydrochloride.
46 . An oral or subcutaneously injectable composition comprising a taxane, an alkyl N,N-disubstituted-amino acetate, and one or more pharmaceutically acceptable carriers.
47 . The composition in accordance with claim 46 wherein the taxane is a member of the group consisting of paclitaxel, docetaxel, tesetaxel, and mixtures thereof.
48 . The composition in accordance with claim 46 wherein the alkyl N,N-disubstituted amino acetate is dodecyl 2-(N,N-dimethylamino) propionate.
49 . The composition in accordance with claim 46 wherein the alkyl N,N-disubstituted amino acetate is dodecyl 2-(N,N-dimethylamino) propionate hydrochloride.
50 . The composition in accordance with claim 46 wherein the taxane is paclitaxel and the alkyl N,N-disubstituted-amino acetate is dodecyl 2-(N,N-dimethylamino) propionate.
51 . The composition in accordance with claim 46 wherein the taxane is paclitaxel and the alkyl N,N-disubstituted-amino acetate is dodecyl 2-(N,N-dimethylamino) propionate hydrochloride.
52 . The composition in accordance with claim 34 wherein the alkyl N,N-disubstituted-amino acetate is dodecyl 2-(N,N-dimethylamino) propionate.
53 . The composition in accordance with claim 35 wherein the alkyl N,N-disubstituted-amino acetate is dodecyl 2-(N,N-dimethylamino) propionate.
54 . The composition in accordance with claim 36 wherein the alkyl N,N-disubstituted-amino acetate is dodecyl 2-(N,N-dimethylamino) propionate hydrochloride.
55 . The composition in accordance with claim 37 wherein the alkyl N,N-disubstituted-amino acetate is dodecyl 2-(N,N-dimethylamino) propionate.
56 . The composition in accordance with claim 8 wherein the alkyl N,N-disubstituted-amino acetate is dodecyl 2-(N,N-dimethylamino) propionate hydrochloride.
57 . The composition in accordance with claim 7 wherein the alkyl N,N-disubstituted-amino acetate is dodecyl 2-(N,N-dimethylamino) propionate hydrochloride.
58 . The composition in accordance with claim 9 wherein the alkyl N,N-disubstituted-amino acetate is dodecyl 2-(N,N-dimethylamino) propionate.
59 . The composition in accordance with claim 9 wherein the alkyl N,N-disubstituted-amino acetate is dodecyl 2-(N,N-dimethylamino) propionate hydrochloride.Cited by (0)
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