Solid compositions comprising a glp-1 agonist and a salt of n-(8-(2-hydroxybenzoyl)amino)caprylic acid
US-2016151462-A1 · Jun 2, 2016 · US
US12514822B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12514822-B2 |
| Application number | US-202519192233-A |
| Country | US |
| Kind code | B2 |
| Filing date | Apr 28, 2025 |
| Priority date | May 2, 2013 |
| Publication date | Jan 6, 2026 |
| Grant date | Jan 6, 2026 |
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The present invention relates to improved uses of glucagon-like peptide 1 (GLP-1) peptides in oral therapy.
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The invention claimed is: 1 . A method for treating type 2 diabetes in a subject in need of such treatment, the method comprising: orally administering to the subject a composition comprising N-epsilon26-[2-(2-{2-[2-(2-{2-[(S)-4-Carboxy-4-(17-carboxyheptadecanoylamino)butyrylamino]ethoxy}ethoxy)acetylamino]ethoxy}ethoxy)acetyl][Aib8,Arg34]GLP-1-(7-37) (semaglutide) and sodium N-(8-(2-hydroxybenzoyl)amino)caprylate (SNAC); wherein the composition comprises 0.5-50 mg of the semaglutide; and wherein the composition is administered such that the ratio between the plasma half-life in days in humans of the semaglutide and the dosing interval in days of the composition is more than 2:1. 2 . The method according to claim 1 , wherein the composition comprises 100 mg of the SNAC. 3 . The method according to claim 1 , wherein the composition comprises 300 mg of the SNAC. 4 . The method according to claim 1 , wherein the composition is in the form of a tablet. 5 . The method according to claim 1 , wherein the semaglutide is the only GLP-1 peptide in the composition. 6 . The method according to claim 5 , wherein the composition comprises 100 mg of the SNAC. 7 . The method according to claim 5 , wherein the composition comprises 300 mg of the SNAC. 8 . The method according to claim 6 or 7 , wherein the composition is in the form of a tablet. 9 . The method according to claim 1 , wherein the subject suffers from obesity. 10 . The composition according to claim 1 , wherein the amount of SNAC is 50-90% (w/w) of the composition.
Mouth and digestive tract, i.e. intraoral and peroral administration · CPC title
having the carbon of a carboxamide group directly attached to the aromatic ring, e.g. procainamide, procarbazine, metoclopramide, labetalol · CPC title
for hyperglycaemia, e.g. antidiabetics · CPC title
Anorexiants; Antiobesity agents · CPC title
Cellulose; Cellulose derivatives, e.g. hydroxypropyl methylcellulose · CPC title
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