Stable injectable compositions of glp-2 peptide
US-2024415933-A1 · Dec 19, 2024 · US
US9821031B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9821031-B2 |
| Application number | US-52227408-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jan 8, 2008 |
| Priority date | Jan 8, 2007 |
| Publication date | Nov 21, 2017 |
| Grant date | Nov 21, 2017 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
This invention relates to methods of treating and ameliorating congenital and neonatal hyperinsulinism and post-prandial hypoglycemia, comprising the step of administering an antagonist of the Glucagon-Like Peptide-1 (GLP-I) receptor, e.g. a GLP-I fragment or analogue thereof.
Opening claim text (preview).
What is claimed is: 1. A method of treating a subject with post-prandial hypoglycemia, comprising the step of subcutaneously administering to said subject an antagonist of the Glucagon Like Peptide-1(GLP-1) receptor, wherein said GLP-1-antagonist is a peptide, wherein the amino acid sequence of the peptide is the amino acid sequence set forth in SEQ ID NO: 1, and wherein said post-prandial hypoglycemia is associated with a gastric surgery. 2. The method of claim 1 , wherein said post-prandial hypoglycemia is associated with a Nissen fundoplication. 3. The method of claim 1 , wherein said post-prandial hypoglycemia is associated with a gastric-bypass surgery. 4. The method of claim 1 , wherein the subject is a pediatric subject. 5. The method of claim 1 , wherein the antagonist is administered at a dosage from 20 nmol/kg/day to 2000 nmol/kg/day. 6. The method of claim 1 , wherein the antagonist is administered at a dosage from 20 nmol/kg/day to 300 nmol/kg/day. 7. The method of claim 1 , wherein the antagonist is administered at a dosage of 100 nmol/kg/day. 8. The method of claim 1 , wherein the antagonist is administered at a dosage of 200 nmol/kg/day. 9. The method of claim 1 , wherein the antagonist is administered at a dosage of 300 nmol/kg/day.
Related publications grouped by family.
Answers are generated from the same data shown on this page.