US2018303899A1PendingUtilityA1
Use of Melanocortins to Treat Insulin Sensitivity
Est. expiryNov 5, 2027(~1.3 yrs left)· nominal 20-yr term from priority
A61P 3/10A61P 43/00A61P 5/50A61P 3/00A61P 3/04C07K 7/64A61K 38/12A61K 38/33A61K 38/04
60
PatentIndex Score
0
Cited by
0
References
0
Claims
Abstract
The present invention relates to peptide ligands of the melanocortin receptors, in particular the melancortin-4 receptor, and as such, are useful in the treatment of disorders responsive to the activation of this receptor, such as insulin resistance.
Claims
exact text as granted — not AI-modified1 - 35 . (canceled)
36 . A method of treating insulin resistance in a subject in need thereof, comprising administration of an effective amount of D-Phe-c(Cys-His-D-(Et)Tyr-hArg-Bip-β-Ala-D-Cys)-Thr-NH 2 (SEQ ID NO:26) or a pharmaceutically acceptable salt thereof.
37 . The method of claim 36 , wherein said subject is a child.
38 . The method of claim 37 , wherein the child is obese.
39 . The method of claim 37 , wherein the child is normal weight or lean.
40 . The method of claim 37 , wherein the child suffers from Type II diabetes.
41 . The method of claim 36 , wherein said subject is an adult.
42 . The method of claim 36 , wherein said subject is an elderly adult.
43 . The method of claim 36 , wherein the D-Phe-c(Cys-His-D-(Et)Tyr-hArg-Bip-β-Ala-D-Cys)-Thr-NH 2 (SEQ ID NO:26) or a pharmaceutically acceptable salt thereof is formulated as a pharmaceutical composition.
44 . The method of claim 43 , wherein said pharmaceutical composition is a sustained release composition.
45 . The method of claim 36 , wherein said administration is oral, subcutaneous, intraperitoneal, intramuscular, intravenous, rectal, transdermal or intranasal.
46 . The method according to claim 36 , wherein said administration is continuous.
47 . A method of treating insulin resistance in a subject in need thereof, comprising administration of an effective amount of a compound selected from the group consisting of:
c[Hydantoin(C(O)-(Asp-His))-D-Phe-Arg-Trp-Lys]-NH 2 (SEQ ID NO: 274) c[Hydantoin(C(O)-(Asp-A 3 c))-D-Phe-Arg-Trp-Lys]-NH 2 ; (SEQ ID NO: 274) c[Hydantoin(C(O)-(Asp-A 5 c))-D-Phe-Arg-Trp-Lys]-NH 2 ; (SEQ ID NO: 274) c[Hydantoin(C(O)-(Asp-A 6 c))-D-Phe-Arg-Trp-Lys]-NH 2 ; (SEQ ID NO: 274) or a pharmaceutically acceptable salt thereof.
48 . The method of claim 47 , wherein said subject is a child.
49 . The method of claim 47 , wherein said subject is an adult.
50 . The method of claim 48 , wherein the child is obese.
51 . The method of claim 48 , wherein the child suffers from Type II diabetes.
52 . The method of claim 47 , wherein the compound or a pharmaceutically acceptable salt thereof is formulated as a pharmaceutical composition.
53 . The method of claim 52 , wherein said pharmaceutical composition is a sustained release composition.
54 . The method of claim 47 , wherein said administration is oral, subcutaneous, intraperitoneal, intramuscular, intravenous, rectal, transdermal or intranasal.
55 . The method according to claim 47 , wherein said administration is continuous.Cited by (0)
No later patents cite this yet.
References (0)
No backward citations on record.