Glucagon analogs exhibiting physiological solubility and stability

• US 8,338,368 B2
• Filed: 11/06/2006
• Issued: 12/25/2012
• Est. Priority Date: 11/07/2005
• Status: Expired due to Fees

• Current Assignee: Indiana University Research & Technology Corporation (Indiana University)
• Original Assignee: Indiana University Research & Technology Corporation (Indiana University)
• Inventors: Dimarchi, Richard D., Smiley, David L.
• Primary Examiner(s): Chandra, Gyan
• Application Number:
  US12/092,802
• Publication Number:
  US 20090137456A1
• Time in Patent Office: 2,241 Days
• Field of Search: None
• US Class Current: 514/7.2
• CPC Class Codes: A61K 38/26 Glucagons
• CPC Class Codes: A61P 3/08 for glucose homeostasis pancreatic hormones A61P5/48
• CPC Class Codes: A61P 3/10 for hyperglycaemia, e.g. antidiabetics
• CPC Class Codes: C07K 14/605 Glucagons
• CPC Class Codes: Y02E 50/10 Biofuels, e.g. bio-diesel

Abstract

Modified glucagon peptides are disclosed having improved solubility and stability, wherein the native glucagon peptide has been modified by pegylation, or the addition of a carboxy terminal peptide selected from the group consisting of SEQ ID NO: 19, SEQ ID NO: 20, SEQ ID NO: 21, or both.

Claims

1. A derivative of native glucagon (SEQ ID NO:

1) comprising a hydrophilic moiety covalently bound to a residue at position 16, 17, or 21, of the derivative, wherein the peptide stimulates activity at the glucagon receptor, and pharmaceutically acceptable salts of said derivative.

2. The derivative of claim 1 wherein said hydrophilic moiety is polyethylene glycol.

3. The derivative of claim 2 wherein the polyethylene glycol chain has a molecular weight selected from the range of about 1,000 to about 5,000 Daltons.

4. The derivative of claim 2 wherein the polyethylene glycol chain has a molecular weight greater than about 5,000 Daltons.

5. The derivative of claim 4 wherein amino acid 29 of the derivative is covalently bound to a second peptide comprising a sequence selected from the group consisting of SEQ ID NO:

19, SEQ ID NO;

20 and SEQ ID NO;

21.

6. The derivative of claim 5, wherein the second peptide is SEQ ID NO:

19 and the terminal amino acid of the derivative comprises an amide group in place of the carboxylic acid group of the native amino acid.

7. A multimer comprising at least two derivatives of claim 1 bound to one another through a linker.

8. A pharmaceutical composition comprising a derivative of claim 1, or pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier.

9. A kit for administering a glucagon agonist to a patient in need thereof, said kit comprising a pharmaceutical composition of claim 8;

and a device for administering said composition to a patient.

10. A method of treating hypoglycemia in a patient, said method comprising the steps of administering an effective amount of a pharmaceutical composition of claim 8 to the patient.

11. The pharmaceutical composition of claim 8, further comprising insulin.

12. The derivative of claim 1, wherein the amino acid residue comprising the hydrophilic moiety is an amino acid selected from the group consisting of lysine, cysteine, ornithine, homocysteine, and acetyl phenylalanine.

13. The derivative of claim 1, wherein the derivative comprises SEQ ID NO:

1 with an amino acid substitution at position 12 and/or position 27.

14. The derivative of claim 1, wherein the derivative comprises an Arg at position 12 and/or a Leu or Norleucine at position 27.

15. The derivative of claim 1, wherein the C-terminal amino acid of the derivative comprises an amide group in place of the carboxylic acid group of the native amino acid.