IP Library Granted Patent US 9,974,837
Granted Patent B2
US 9,974,837 · App. 15/286,279 · Granted May 22, 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 9,974,837
App. No.
15/286,279
Granted
May 22, 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 without inflammatory bowel disease, 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 without inflammatory bowel disease, 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 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 said patient is an adult and 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 said patient is an adult and 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 042468/0898 →
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 20170028027A1 · Feb 2, 2017