US2016022781A1PendingUtilityA1
Methods for administering hypoglycemic agents
Est. expiryNov 4, 2025(expired)· nominal 20-yr term from priority
A61P 3/10A61P 3/04A61K 38/385A61K 45/06A61K 31/426A61K 31/64A61K 38/28A61K 31/155A61K 38/26A61K 9/0019
42
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Claims
Abstract
The present invention relates to methods of administering hypoglycemic agents and/or GLP-1 agonists.
Claims
exact text as granted — not AI-modifiedWe claim:
1 . A method for treating a disease selected from the group consisting of Type 1 diabetes, Type II diabetes, obesity and hyperglycemia in a human in need thereof comprising administering a composition comprising a polypeptide having GLP-1 activity as a subcutaneous injection once weekly to said human via an injection device comprising a tube having a gauge of 28, 29 or, 30 wherein the composition comprises about 0.01 mg to about 104 mg of the polypeptide having GLP-1 activity and wherein the polypeptide having GLP-1 activity comprises two fragment and variant polypeptides of human GLP-1, wherein said fragment and variant polypeptides of human GLP-1 are tandemly oriented and covalently bound by a chemical linker.
2 . The method of claim 1 wherein the disease is Type II diabetes.
3 . The method of claim 1 wherein the needle has a gauge selected from is 29.
4 . The method of claim 1 , wherein said two fragment and variant polypeptides of human GLP-1 are separated by other amino acids sequences.
5 . The method of claim 1 wherein the chemical linker is a disulphide bond.
6 . The method of claim 1 , wherein the fragment and variant polypeptides of human GLP-1 comprise a substitution of the alanine residue analogous to alanine 8 of wild type GLP-1.
7 . The method of claim 7 wherein the alanine at position 8 is substituted with glycine.
8 . The method of claim 1 wherein the polypeptide is administered to said human at a dose selected from about 0.5 mg/week, 0.8 mg/week, 1.0 mg/week and 2 mg/week.
9 . The method of claim 1 wherein the GLP-1 activity is selected from stimulating glucose-dependent insulin secretion, suppressing glucagon secretion, delaying gastric emptying, and promoting beta cell competence and neogenesis.Cited by (0)
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