IP Library Granted Patent US 9,593,149
Granted Patent B2
US 9,593,149 · App. 15/151,093 · Granted Mar 14, 2017

Amylin and calcitonin receptor agonist

Inventors: Thomas Kruse (Herlev, DK); Lauge Schaeffer (Lyngby, DK); Kirsten Dahl (Smoerum, DK); Kirsten Raun (Lyngby, DK)
Assignee: Novo Nordisk A/S
C07K14/001C07K14/575A61K38/00
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Quick Facts
Patent No.
US 9,593,149
App. No.
15/151,093
Granted
Mar 14, 2017
Kind
B2
Abstract

The present invention relates to peptides comprising an amino acid sequence SEQ ID NO: 1 (EASELSTAALGRLSAELHELATLPRTETGPESP), analogs and derivatives thereof and pharmaceutical compositions comprising such peptides and derivatives. This invention further regards the use of these peptides according to SEQ ID NO: 1, analogs and derivatives thereof as medicaments.

Claims (15)

1. A peptide comprising the amino acid sequence of EASELSTAALGRLSAELHELATLPRTETGPESP (SEQ ID NO:1).

2. The peptide according to claim 1 , comprising a C-terminal amide group.

3. A derivative of the peptide according to claim 1 , wherein said derivative comprises a side chain covalently attached to the peptide at its N-terminal and wherein said side chain comprises fatty acid or fatty diacid.

4. The derivative according to claim 3 , wherein said fatty acid or fatty diacid comprises between 14 to 20 carbon atoms.

5. The derivative according to claim 3 , wherein said side chain further comprises a linker.

6. The derivative according to claim 5 , wherein said linker is selected from the group consisting of gGlu, gGlu-OEG, gGlu-OEG-OEG, gGlu-OEG-OEG-OEG, gGlu-OEG-OEG-OEG-OEG, and gGlu-OEG-OEG-OEG-OEG-OEG.

7. A derivative of the peptide according to claim 2 , wherein said derivative comprises a side chain covalently attached to the peptide at its N-terminal and wherein said side chain comprises fatty acid or fatty diacid.

8. The derivative according to claim 7 , wherein said fatty acid or fatty diacid comprises between 14 to 20 carbon atoms.

9. The derivative according to claim 7 , wherein said side chain further comprises a linker.

10. The derivative according to claim 9 , wherein said linker is selected from the group consisting of gGlu, gGlu-OEG, gGlu-OEG-OEG, gGlu-OEG-OEG-OEG, gGlu-OEG-OEG-OEG-OEG, and gGlu-OEG-OEG-OEG-OEG-OEG.

11. A compound which is

12. A pharmaceutical composition comprising the compound of claim 11 and a pharmaceutically acceptable excipient.

13. A method of reducing food intake comprising administering a pharmaceutically effective amount of the compound of claim 11 to a subject in need thereof.

14. A method of treating overweight comprising administering a pharmaceutically effective amount of the compound of claim 11 to a subject in need thereof.

15. A method of treating obesity comprising administering a pharmaceutically effective amount of the compound of claim 11 to a subject in need thereof.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 23, 2016
From: KRUSE, THOMAS; SCHAEFFER, LAUGE; DAHL, KIRSTEN; POULSEN, CHRISTIAN; RAUN, KIRSTEN
To: NOVO NORDISK A/S
Reel/Frame 038994/0211 →
Priority Claims (1)
EP 14183551 · Sep 4, 2014 · regional
Continuity (2)
Continuation PCTEP2015069996 · Sep 2, 2015
Related Publication 20160272683A1 · Sep 22, 2016