IP Library › Granted Patent US 8,575,091
Granted Patent B1
US 8,575,091 · App. 13/930,075 · Granted Nov 5, 2013

Amylin analogues and pharmaceutical compositions thereof

Inventors: Kirsten Dahl (Smoerum, DK); Lauge Schaeffer (Lyngby, DK); Thomas Kruse (Herlev, DK)
Assignee: Novo Nordisk A/S
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Quick Facts
Patent No.
US 8,575,091
App. No.
13/930,075
Granted
Nov 5, 2013
Kind
B1
Abstract

The invention relates to polypeptides comprising an amino acid sequence which is an analogue of human amylin, pharmaceutical compositions comprising these polypeptides, and these polypeptides for use as medicaments.

Claims (13)

1. A polypeptide comprising SEQ ID NO: 4.

2. The polypeptide of claim 1 , wherein at least one substituent is attached to at least one amino acid residue of said polypeptide.

3. The polypeptide of claim 2 , wherein the substituent is selected from the group consisting of C20diacid, C20diacid-γGlu, C20diacid-γGlu-γGlu, C20diacid-γGlu-γGlu-γGlu, C20diacid-OEG, C20diacid-γGlu-OEG, C20diacid-γGlu-OEG-OEG, C16diacid-γGlu, and C14diacid-γGlu.

4. The polypeptide of claim 2 , wherein the substituent is attached to the α-amino group of the N-terminal amino acid residue or to a Lys residue.

5. The polypeptide of claim 2 , wherein the substituent is only attached to a Lys residue at position 1.

6. The polypeptide of claim 2 , wherein the substituent is attached to a lysine residue via the ε-amino group.

7. The polypeptide according to claim 1 , wherein the polypeptide is N ε1 -[(4S)-4-carboxy-4-[[(4S)-4-carboxy-4-(19-carboxynonadecanoylamino)butanoyl]amino]butanoyl]-[Asp14,Arg17,Pro21,Pro27,Arg35]-h-amylin.

8. A pharmaceutical composition comprising the polypeptide of claim 1 and a pharmaceutical acceptable excipient.

9. A process for preparing a pharmaceutical composition comprising mixing the polypeptide of claim 1 with a pharmaceutically acceptable excipient.

10. A method of treating type 2 diabetes or obesity comprising administering the polypeptide of claim 1 .

11. A pharmaceutical composition comprising the polypeptide of claim 7 and a pharmaceutical acceptable excipient.

12. A process for preparing a pharmaceutical composition comprising mixing the polypeptide of claim 7 with a pharmaceutically acceptable excipient.

13. A method of treating type 2 diabetes or obesity comprising administering the polypeptide of claim 7 .

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 17, 2013
From: DAHL, KIRSTEN; SCHAEFFER, LAUGE; KRUSE, THOMAS
To: NOVO NORDISK A/S
Reel/Frame 031217/0965 →
Priority Claims (1)
EP 12164692 · Apr 19, 2012 · regional
Continuity (2)
Continuation PCTEP2013058165 · Apr 19, 2013
Provisional Application 61637806 · Apr 24, 2012