US2020376085A1PendingUtilityA1
Treatment of short bowel syndrome patients with colon-in-continuity
Assignee: SHIRE NPS PHARMACEUTICALS INCPriority: Nov 1, 2004Filed: Aug 21, 2020Published: Dec 3, 2020
Est. expiryNov 1, 2024(expired)· nominal 20-yr term from priority
A61P 1/02A61K 38/26A61B 5/4222A61K 9/0019A61P 1/00
78
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Claims
Abstract
Intestinal absorption is enhanced in short bowel syndrome patients presenting with colon-in-continuity by treatment with a GLP-2 receptor agonist, such as teduglutide.
Claims
exact text as granted — not AI-modifiedWhat is claimed is:
1 . A method for treating an adult human patient with short bowel syndrome who is dependent on parenteral nutrition and who presents with colon-in-continuity with remnant small intestine, said method comprising administering to the patient [Gly2]hGLP-2 using a dosing regimen effective to reduce the dependency on parenteral nutrition by the patient.
2 . The method of claim 1 , wherein the [Gly2]hGLP-2 is administered at a daily dose of from 5 to 500 μg/kg.
3 . The method of claim 2 , wherein the [Gly2]hGLP-2 is administered at a daily dose of from 30 to 150 μg/kg.
4 . The method of claim 1 , wherein the [Gly2]hGLP-2 is administered by subcutaneous injection.
5 . The method of claim 4 , wherein the subcutaneous injection is into the abdomen, thigh, or arm.
6 . The method of claim 1 , wherein the reduction on dependency is a decrease in the amount of parenteral nutrition received by the patient.
7 . The method of claim 1 , wherein the reduction on dependency is a decrease in days or weeks of parenteral nutrition received by the patient.
8 . A method for treating an adult human patient with short bowel syndrome who is dependent on parenteral nutrition and who presents with colon-in-continuity with remnant small intestine, comprising administering to the patient [Gly2]hGLP-2 using a dosing regimen effective to reduce the dependency on parenteral nutrition by the patient; wherein the [Gly2]hGLP-2 is administered daily at a dose of from 30 to 150 μg/kg by subcutaneous injection into the abdomen, thigh, or arm.
9 . The method of claim 8 , wherein the reduction on dependency is a decrease in the amount of parenteral nutrition received by the patient or a decrease in days or weeks of parenteral nutrition received by the patient.
10 . The method of claim 1 , wherein said regimen comprises administration of said [Gly2]hGLP-2 over a period of at least 21 days.
11 . The method of claim 8 , wherein said regimen comprises administration of said [Gly2]hGLP-2 over a period of at least 21 days.Join the waitlist — get patent alerts
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