IP Library Granted Patent US 10,119,132
Granted Patent B2
US 10,119,132 · App. 14/948,890 · Granted Nov 6, 2018

Long-acting coagulation factors and methods of producing same

Inventors: Udi Eyal Fima (Dvira, IL); Gili Hart (Shoham, IL)
Assignee: OPKO Biologics Ltd.
C12N9/6437C07K14/505C07K14/59C07K14/745C12N9/644C12N9/96C12Y304/21021A61K38/00A61K38/4846C07K2319/31
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 10,119,132
App. No.
14/948,890
Granted
Nov 6, 2018
Kind
B2
Abstract

Polypeptides comprising at least one carboxy-terminal peptide (CTP) of chorionic gonadotrophin attached to the carboxy terminus but not to the amino terminus of a coagulation factor and polynucleotides encoding the same are disclosed. Pharmaceutical compositions comprising the polypeptides and polynucleotides of the invention and methods of using and producing same are also disclosed.

Claims (21)

1. A method of treating hemophilia A in a subject, the method comprising administering a CTP-modified Factor VII (FVII) polypeptide to said subject, wherein said CTP-modified Factor VII (FVII) polypeptide consists of a coagulation Factor VII (FVII) polypeptide and three chorionic gonadotropin carboxy terminal peptides (CTPs) attached to the carboxy terminus of said coagulation FVII polypeptide, thereby treating said hemophilia A.

2. The method of claim 1 , wherein at least one CTP consists of the amino acid sequence selected from the group consisting of: SEQ ID NO: 1 and SEQ ID NO: 2.

3. The method of claim 1 , wherein at least one CTP is glycosylated.

4. The method of claim 1 , wherein at least one CTP is attached to said coagulation Factor VII polypeptide via a linker.

5. The method of claim 4 , wherein said linker is a peptide bond.

6. The method of claim 1 , wherein the sequence of said CTP-modified FVII polypeptide is selected from the group consisting of SEQ ID NO: 25 and SEQ ID NO: 46.

7. The method of claim 1 , wherein said coagulation FVII polypeptide is an activated coagulation FVII (FVIIa) polypeptide.

8. The method of claim 7 , wherein said activated coagulation FVII polypeptide is in the form of a disulfide-linked two chain heterodimer.

9. The method of claim 1 , wherein the subject is a human child.

10. The method of claim 1 , wherein said administering is via the subcutaneous route.

11. A method of treating hemophilia B in a subject, the method comprising the step of administering to the subject a CTP-modified Factor IX (FIX) polypeptide, wherein the CTP-modified Factor IX (FIX) polypeptide consists of a coagulation Factor IX (FIX) polypeptide and three chorionic gonadotrophin carboxy terminal peptides (CTPs) attached to the carboxy terminus of said coagulation FIX polypeptide, thereby treating said hemophilia B in said subject.

12. The method of claim 11 , wherein the sequence of said CTP-modified Factor IX (FIX) polypeptide is selected from the group consisting of SEQ ID NO: 31 and SEQ ID NO: 48.

13. The method of claim 11 , wherein at least one CTP consists of the amino acid sequence selected from the group consisting of: SEQ ID NO: 1 and SEQ ID NO: 2.

14. The method of claim 11 , wherein at least one CTP is glycosylated.

15. The method of claim 11 , wherein at least one CTP is truncated.

16. The method of claim 11 , wherein at least one CTP is attached to said coagulation FIX polypeptide via a linker.

17. The method of claim 16 , wherein said linker is a peptide bond.

18. The method of claim 11 , wherein said coagulation FIX polypeptide is an activated coagulation FIX (FIXa) polypeptide.

19. The method of claim 18 , wherein said activated coagulation FIX polypeptide is in the form of a disulfide-linked two chain heterodimer.

20. The method of claim 11 , wherein the subject is a human child.

21. The method of claim 11 , wherein said administering is via the subcutaneous route.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 30, 2017
From: FIMA, UDI EYAL; HART, GILI
To: OPKO BIOLOGICS LTD.
Reel/Frame 041115/0885 →
Continuity (6)
Division 13932839 · Jul 1, 2013
Continuation In Part 13759860 · Feb 5, 2013
Continuation In Part 13372540 · Feb 14, 2012
Continuation In Part 12826754 · Jun 30, 2010
Provisional Application 61224366 · Jul 9, 2009
Related Publication 20160076018A1 · Mar 17, 2016
Cited By (2)
US 12,203,113 US 12,459,982