US2022125766A1PendingUtilityA1
Methods for treating congenital disorders of glycosylation
Est. expiryAug 20, 2038(~12 yrs left)· nominal 20-yr term from priority
Inventors:Ethan Oren PerlsteinJessica P. LaoFeba SamNina DiprimioZachary PartonHillary TsangKausalya MurthySangeetha Venkatraman IyerJoshua MastTamy May Sharly Portillo RodriguezMadeleine Prangley
A61K 31/352A61K 31/192A61P 3/00A61K 31/353A61K 31/136A61K 31/277A61P 35/00A61K 31/426A61K 31/085A61K 31/185A61P 37/00A61K 31/122A61K 31/137A61K 31/198A61K 45/06
44
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Claims
Abstract
The present disclosure relates generally to compounds and pharmaceutical compositions for increasing glycosylation and treating congenital disorders of glycosylation.
Claims
exact text as granted — not AI-modified1 .- 37 . (canceled)
38 . A method for treating a congenital disorder of glycosylation in a patient in need thereof comprising administering a therapeutically effective amount of an aldose reductase inhibitor.
39 . (canceled)
40 . A method for treating phosphomannomutase deficiency in a patient in need thereof comprising administering a therapeutically effective amount of an aldose reductase inhibitor.
41 . (canceled)
42 . The method of claim 38 , wherein the aldose reductase inhibitor is epalrestat.
43 . The method of claim 38 , wherein the patient is further administered a therapeutically effective amount of another therapeutic agent, wherein the another therapeutic agent is an aldose reductase inhibitor.
44 . The method of claim 43 , wherein the another therapeutic agent is selected from: α-cyano-4-hydroxycinnamic acid, alrestatin, fidarestat, imirestat, lidorestat, minalrestat, ponalrestat, ranirestat, sorbinil, tolrestat, zenarestat, zopolrestat, epalrestat, and rhetsinine, or a pharmaceutically acceptable salt thereof.
45 . The method of claim 38 , wherein the congenital disorder of glycosylation is a N-linked glycosylation disorder.
46 . The method of claim 38 , wherein the aldose reductase inhibitor is a compound, or a pharmaceutically acceptable salt thereof, having a —CO 2 H group and an aromatic ring.
47 . The method of claim 40 , wherein the aldose reductase inhibitor is a compound, or a pharmaceutically acceptable salt thereof, having a —CO 2 H group and an aromatic ring.
48 . The method of claim 45 , wherein the aldose reductase inhibitor is a compound, or a pharmaceutically acceptable salt thereof, having a —CO 2 H group and an aromatic ring.
49 . The method of claim 47 , wherein the patient is further administered a therapeutically effective amount of another therapeutic agent, wherein the another therapeutic agent is an aldose reductase inhibitor.
50 . The method of claim 38 , wherein the aldose reductase inhibitor is administered as a pharmaceutical composition.
51 . The method of claim 40 , wherein the aldose reductase inhibitor is administered as a pharmaceutical composition.
52 . The method of claim 50 , wherein the pharmaceutical composition is formulated to provide a sustained or delayed release of the aldose reductase inhibitor.
53 . The method of claim 51 , wherein the pharmaceutical composition is formulated to provide a sustained or delayed release of the aldose reductase inhibitor.
54 . The method of claim 38 , wherein the aldose reductase inhibitor is administered once, twice, or three times daily.
55 . The method of claim 40 , wherein the aldose reductase inhibitor is administered once, twice, or three times daily.Join the waitlist — get patent alerts
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