US2020164041A1PendingUtilityA1
Treatment of short bowel syndrome patients with colon-in-continuity
Assignee: SHIRE NPS PHARMACEUTICALS INCPriority: Nov 1, 2004Filed: Jan 24, 2020Published: May 28, 2020
Est. expiryNov 1, 2024(expired)· nominal 20-yr term from priority
A61P 1/00A61B 5/4222A61K 38/26A61K 9/0019A61P 1/02
76
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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-modified1 . A method of treating an adult human patient having short bowel syndrome with colon-in-continuity and remnant small intestine ranging from about 25 cm to about 200 cm and who receives an amount of parenteral nutrition each week, said method comprising administering [Gly2]hGLP-2 to said patient using a dosing regimen effective to reduce or eliminate said weekly amount of parenteral nutrition received by said patient.
2 . The method as defined in claim 1 , wherein the [Gly2]hGLP-2 is administered at a daily dose of from 5 to 500 μg/kg.
3 . The method as defined in claim 2 , wherein the [Gly2]hGLP-2 is administered at a daily dose of from 30 to 150 μg/kg.
4 . The method as defined in claim 1 , wherein the [Gly2]hGLP-2 is administered by subcutaneous injection.
5 . The method as defined in claim 4 , wherein the subcutaneous injection is into the abdomen, thigh, or arm.
6 . The method as defined in claim 1 , wherein said patient has a length of small intestine ranging from about 50 to 150 cm.
7 . A method of treating an adult human patient having short bowel syndrome with colon-in-continuity and remnant small intestine ranging from about 25 cm to about 200 cm and who receives an amount of parenteral nutrition each week, said method comprising administering [Gly2]hGLP-2 to said patient using a dosing regimen effective to increase wet weight absorption compared to a baseline wet weight absorption by said patient.
8 . The method as defined in claim 7 , wherein the [Gly2]hGLP-2 is administered at a daily dose of from 5 to 500 μg/kg.
9 . The method as defined in claim 8 , wherein the [Gly2]hGLP-2 is administered at a daily dose of from 30 to 150 μg/kg.
10 . The method as defined in claim 7 , wherein the [Gly2]hGLP-2 is administered by subcutaneous injection.
11 . The method as defined in claim 10 , wherein the subcutaneous injection is into the abdomen, thigh, or arm.
12 . The method as defined in claim 7 , wherein said patient has a length of small intestine ranging from about 50 to 150 cm.
13 . The method as defined in claim 7 , wherein the [Gly2]hGLP-2 is administered at a daily dose of from 5 to 500 μg/kg.
14 . The method as defined in claim 8 , wherein the [Gly2]hGLP-2 is administered at a daily dose of from 30 to 150 μg/kg.
15 . The method as defined in claim 7 , wherein the [Gly2]hGLP-2 is administered by subcutaneous injection.
16 . The method as defined in claim 10 , wherein the subcutaneous injection is into the abdomen, thigh, or arm.
17 . The method as defined in claim 7 , wherein said patient has a length of small intestine ranging from about 50 to 150 cm.
18 . The method as defined in claim 1 , wherein said regimen comprises administration of the [Gly2]hGLP-2 over a period of at least 21 days.
19 . The method as defined in claim 7 , wherein said regimen comprises administration of the [Gly2]hGLP-2 over a period of at least 21 days.
20 . The method as defined in claim 1 , wherein the parenteral nutrition is reduced by volume or frequency of administration.Join the waitlist — get patent alerts
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