IP Library Granted Patent US 8,507,428
Granted Patent B2
US 8,507,428 · App. 13/331,816 · Granted Aug 13, 2013

Glucagon analogs exhibiting GIP receptor activity

Inventors: Richard D. DiMarchi (Carmel, IN); Brian P. Ward (Lebanon, IN)
Assignee: Indiana University Research and Technology Corporation
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Quick Facts
Patent No.
US 8,507,428
App. No.
13/331,816
Granted
Aug 13, 2013
Kind
B2
Abstract

Provided herein are glucagon analogs which exhibit potent activity at the GIP receptor, and, as such are contemplated for use in treating diabetes and obesity. In exemplary embodiments, the glucagon analog of the present disclosures exhibit an EC50 at the GIP receptor which is within the nanomolar or picomolar range.

Claims (22)

1. A peptide comprising

(a) the sequence of SEQ ID NO: 28

(b) SEQ ID NO: 28 with up to 3 amino acid modifications relative to SEQ ID NO: 28, wherein the peptide exhibits agonist activity at each of the human GIP receptor, the human GLP-1 receptor and the human glucagon receptor.

2. The peptide of claim 1 , wherein the peptide has less than 100-fold selectivity for the human GLP-1 receptor versus the GIP receptor.

3. A dimer or multimer or conjugate comprising the peptide of claim 1 , wherein the conjugate further comprises a conjugate moiety, wherein the dimer or multimer comprises two or more of said peptides.

4. A pharmaceutical composition comprising the peptide of claim 1 , or a dimer or multimer or a conjugate comprising the peptide of claim 1 , or a combination thereof, and a pharmaceutically acceptable carrier, diluent, or excipient.

5. A method of reducing weight gain or inducing weight loss in a subject in need thereof, comprising administering to a patient in need thereof a pharmaceutical composition of claim 4 in an amount effective to reduce weight gain or induce weight loss.

6. A method of treating diabetes, comprising administering to a patient in need thereof a pharmaceutical composition of claim 4 in an amount effective to lower blood glucose levels.

7. A peptide comprising the sequence of SEQ ID NO: 28.

8. A pharmaceutical composition comprising the peptide of claim 7 and a pharmaceutically acceptable carrier, diluent, or excipient.

9. A method of reducing weight gain or inducing weight loss in a subject in need thereof, comprising administering to a patient in need thereof a pharmaceutical composition of claim 8 in an amount effective to reduce weight gain or induce weight loss.

10. A method of treating diabetes, comprising administering to a patient in need thereof a pharmaceutical composition of claim 8 in an amount effective to lower blood glucose levels.

11. An analog comprising a parent sequence with a total of up to 3 amino acid modifications relative to the parent sequence, wherein the parent sequence is SEQ ID NO: 28, wherein the amino acid modifications are selected from the group consisting of:

a DPP-IV protective amino acid at position 2; other than AIB, optionally D-Ser;

b. a large, aliphatic, nonpolar amino acid at position 12, optionally Ile;

c. an amino acid other than Arg at position 17, optionally Gln;

d. a small aliphatic amino acid at position 18, other than Ala;

e. an amino acid other than Asp at position 21, optionally Glu;

f. an amino acid other than Gln at position 24, optionally Asn or Ala;

g. an amino acid other than Leu at position 27;

h. an amino acid other than Asp at position 28, optionally Ala; and

i. an amino acid other than Gly at position 29.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 9, 2012
From: DIMARCHI, RICHARD D.; WARD, BRIAN
To: INDIANA UNIVERSITY RESEARCH AND TECHNOLOGY CORPORATION
Reel/Frame 027499/0232 →
Continuity (3)
Provisional Application 61426285 · Dec 22, 2010
Provisional Application 61514609 · Aug 3, 2011
Related Publication 20120238493A1 · Sep 20, 2012