IP Library Granted Patent US 9,981,016
Granted Patent B2
US 9,981,016 · App. 15/286,402 · Granted May 29, 2018

Treatment of short bowel syndrome patients with colon-in-continuity

Inventors: Elizabeth L. Sanguinetti (Salt Lake City, UT); Thomas B. Marriott (Sandy, UT); Jennifer Lopansri (Park City, UT); Consuelo M. Blosch (Seattle, WA)
Assignee: Shire-NPS Pharmaceuticals, Inc.
A61K38/26A61K9/0019
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Quick Facts
Patent No.
US 9,981,016
App. No.
15/286,402
Granted
May 29, 2018
Kind
B2
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 (15)

1. A method of treating an adult human patient having short bowel syndrome secondary to multiple strictures due to adhesions or radiation, 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 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. A method of treating an adult human patient having short bowel syndrome secondary to multiple strictures due to adhesions or radiation, who receives an amount of parenteral nutrition each week, and who presents with colon-in-continuity with remnant small intestine, said method comprising administering a [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.

7. The method as defined in claim 6 , wherein the [Gly2]hGLP-2 is administered at a daily dose of from 5 to 500 μg/kg.

8. The method as defined in claim 7 , wherein the [Gly2]hGLP-2 is administered at a daily dose of from 30 to 150 μg/kg.

9. The method as defined in claim 6 , wherein the [Gly2]hGLP-2 is administered by subcutaneous injection.

10. The method as defined in claim 9 , wherein the subcutaneous injection is into the abdomen, thigh, or arm.

11. 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.

12. The method as defined in claim 6 , wherein said regimen comprises administration of the [Gly2]hGLP-2 over a period of at least 21 days.

13. The method as defined in claim 1 , wherein the parenteral nutrition is reduced by volume or frequency of administration.

14. The method as defined in claim 1 , wherein the [Gly2]hGLP-2 is administered at a daily dose of from 30 to 150 μg/kg by subcutaneous injection.

15. The method as defined in claim 6 , wherein the [Gly2]hGLP-2 is administered at a daily dose of from 30 to 150 μg/kg by subcutaneous injection.

Assignments (4)
CHANGE OF ADDRESS Recorded May 16, 2017
From: SHIRE-NPS PHARMACEUTICALS, INC.
To: SHIRE-NPS PHARMACEUTICALS, INC.
Reel/Frame 042467/0012 →
CHANGE OF NAME Recorded Dec 20, 2016
From: NPS PHARMACEUTICALS, INC.
To: SHIRE-NPS PHARMACEUTICALS, INC.
Reel/Frame 041033/0252 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 9, 2016
From: SANGUINETTI, ELIZABETH L; MARRIOTT, THOMAS B; LOPANSRI, JENNIFER; BLOSCH, CONSUELO M
To: NPS ALLELIX CORP
Reel/Frame 040267/0729 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 9, 2016
From: NPS ALLELIX CORP.
To: NPS PHARMACEUTICALS, INC.
Reel/Frame 040267/0948 →
Continuity (5)
Continuation 14745157 · Jun 19, 2015
Division 12938117 · Nov 2, 2010
Division 11262980 · Nov 1, 2005
Provisional Application 60623233 · Nov 1, 2004
Related Publication 20170020983A1 · Jan 26, 2017