IP Library Granted Patent US 9,156,902
Granted Patent B2
US 9,156,902 · App. 13/494,484 · Granted Oct 13, 2015

Glucagon/GLP-1 receptor co-agonists

Inventors: Richard D. DiMarchi (Carmel, IN); David L. Smiley (Bloomington, IN)
Assignee: Indiana University Research and Technology Corporation
C07K14/605A61K38/26A61K47/48169A61K47/48176A61K47/48215A61K47/48415A61K49/00G01N33/74A61K38/00C07K2319/00G01N2333/605G01N2800/042G01N2800/085G01N2800/2821G01N2800/2835
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Quick Facts
Patent No.
US 9,156,902
App. No.
13/494,484
Granted
Oct 13, 2015
Kind
B2
Abstract

Provided herein are peptides and variant peptides that exhibit enhanced activity at the GLP-1 receptor, as compared to native glucagon.

Claims (28)

1. A peptide comprising the amino acid sequence of SEQ ID NO: 17, or a pharmaceutically acceptable salt thereof.

2. A pharmaceutical composition comprising the peptide of claim 1 , or a pharmaceutically acceptable salt thereof; and a pharmaceutically acceptable carrier.

3. The pharmaceutical composition of claim 2 , additionally comprising an anti-diabetic or anti-obesity agent.

4. A method of treating a disease or medical condition in a patient in need thereof, wherein the disease or medical condition is selected from the group consisting of: metabolic syndrome, diabetes, obesity, and liver steatosis, comprising administering to the patient the pharmaceutical composition of claim 3 in an amount effective to treat the disease or medical condition.

5. The method of claim 4 , wherein the disease or medical condition is type II diabetes.

6. A method of treating a disease or medical condition in a patient in need thereof, wherein the disease or medical condition is selected from the group consisting of: metabolic syndrome, diabetes, obesity, and liver steatosis, comprising administering to the patient the pharmaceutical composition of claim 2 in an amount effective to treat the disease or medical condition.

7. The method of claim 6 , wherein the disease or medical condition is type II diabetes.

8. A peptide comprising the amino acid sequence of SEQ ID NO: 17.

9. A pharmaceutical composition comprising the peptide of claim 8 ; and a pharmaceutically acceptable carrier.

10. The pharmaceutical composition of claim 9 , additionally comprising an anti-diabetic or anti-obesity agent.

11. A method of treating a disease or medical condition in a patient in need thereof, wherein the disease or medical condition is selected from the group consisting of: metabolic syndrome, diabetes, obesity, and liver steatosis, comprising administering to the patient the pharmaceutical composition of claim 10 in an amount effective to treat the disease or medical condition.

12. The method of claim 11 , wherein the disease or medical condition is type II diabetes.

13. A method of treating a disease or medical condition in a patient in need thereof, wherein the disease or medical condition is selected from the group consisting of: metabolic syndrome, diabetes, obesity, and liver steatosis, comprising administering to the patient the pharmaceutical composition of claim 9 in an amount effective to treat the disease or medical condition.

14. The method of claim 13 , wherein the disease or medical condition is type II diabetes.

15. A peptide consisting of the amino acid sequence of SEQ ID NO: 17 or a pharmaceutically acceptable salt thereof.

16. A pharmaceutical composition comprising the peptide of claim 15 , or a pharmaceutically acceptable salt thereof; and a pharmaceutically acceptable carrier.

17. The pharmaceutical composition of claim 16 , additionally comprising an anti-diabetic or anti-obesity agent.

18. A method of treating a disease or medical condition in a patient in need thereof, wherein the disease or medical condition is selected from the group consisting of: metabolic syndrome, diabetes, obesity, and liver steatosis, comprising administering to the patient the pharmaceutical composition of claim 17 in an amount effective to treat the disease or medical condition.

19. A method of treating a disease or medical condition in a patient in need thereof, wherein the disease or medical condition is selected from the group consisting of: metabolic syndrome, diabetes, obesity, and liver steatosis, comprising administering to the patient the pharmaceutical composition of claim 16 in an amount effective to treat the disease or medical condition.

20. The method of claim 19 , wherein the disease or medical condition is type II diabetes.

21. The method of claim 18 , wherein the disease or medical condition is type II diabetes.

22. A peptide consisting of the amino acid sequence of SEQ ID NO: 17.

23. A pharmaceutical composition comprising the peptide of claim 22 ; and a pharmaceutically acceptable carrier.

24. The pharmaceutical composition of claim 23 , additionally comprising an anti-diabetic or anti-obesity agent.

25. A method of treating a disease or medical condition in a patient in need thereof, wherein the disease or medical condition is selected from the group consisting of: metabolic syndrome, diabetes, obesity, and liver steatosis, comprising administering to the patient the pharmaceutical composition of claim 24 in an amount effective to treat the disease or medical condition.

26. The method of claim 25 , wherein the disease or medical condition is type II diabetes.

27. A method of treating a disease or medical condition in a patient in need thereof, wherein the disease or medical condition is selected from the group consisting of: metabolic syndrome, diabetes, obesity, and liver steatosis, comprising administering to the patient the pharmaceutical composition of claim 23 in an amount effective to treat the disease or medical condition.

28. The method of claim 27 , wherein the disease or medical condition is type II diabetes.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 6, 2012
From: DIMARCHI, RICHARD D.; SMILEY, DAVID L.
To: INDIANA UNIVERSITY RESEARCH AND TECHNOLOGY CORPORATION
Reel/Frame 028497/0500 →
Continuity (3)
Provisional Application 61500027 · Jun 22, 2011
Provisional Application 61547360 · Oct 14, 2011
Related Publication 20120329708A1 · Dec 27, 2012