US2020164040A1PendingUtilityA1

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
A61K 38/26A61P 1/02A61B 5/4222A61K 9/0019A61P 1/00
77
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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-modified
1 . A method of treating an adult human patient having short bowel syndrome with less (as compared to a normal healthy individual), but some detectable, GLP-2 producing tissue in the remnant small intestine, who receives an amount of parenteral nutrition each week, and who presents with colon-in-continuity with remnant small intestine, said method comprising administering [Gly2]hGLP-2 to said patient using a dosing regimen effective to increase the amount of a tissue in the remnant small intestine of 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 regimen comprises administration of said [Gly2]hGLP-2 over a period of at least 21 days. 
     
     
         7 . The method as defined in  claim 1 , wherein said [Gly2]hGLP-2 is administered at a daily dose of from 30 to 150 pg/kg by subcutaneous injection.

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