Factor IX polypeptides and methods of use thereof
The present invention provides methods of administering Factor IX; methods of administering chimeric and hybrid polypeptides comprising Factor IX; polynucleotides encoding such chimeric and hybrid polypeptides; cells comprising such polynucleotides; and methods of producing such chimeric and hybrid polypeptides using such cells.
1. A method of treating hemophilia B comprising intravenously administering to a human subject in need thereof multiple doses of about 50 IU/kg to about 100 IU/kg of a chimeric factor IX (“FIX”) polypeptide comprising human FIX having an amino acid sequence identical to amino acids 1 to 415 of SEQ ID NO:2 and an FcRn binding partner (“FcRn BP”) at a dosing interval of about 10 days to about 14 days between two doses, wherein the FcRn BP is human albumin, wherein the administration treats the human subject by reducing the frequency of spontaneous bleeding.
2. The method of claim 1 , wherein the chimeric FIX polypeptide further comprises a linker joining the FIX and the human albumin.
3. The method of claim 2 , wherein the linker joins the FIX to the N-terminal end of the human albumin.
4. The method of claim 3 , wherein the dosing interval is 14 days and each of the multiple doses is 50 IU/kg to 100 IU/kg.
5. The method of claim 1 , wherein the subject exhibits the plasma FIX activity above 1 IU/dL during the dosing interval as measured by a one stage clotting assay that determines activated partial thromboplastin time.
6. The method of claim 5 , wherein the chimeric FIX polypeptide further comprises a linker joining the FIX and the human albumin.
7. The method of claim 6 , wherein the linker joins the FIX and N-terminal end of the human albumin.
8. The method of claim 7 , wherein the dosing interval is 14 days and each of the multiple doses is 50 IU/kg to 100 IU/kg.
9. A method of treating hemophilia B comprising intravenously administering to a human subject in need thereof multiple doses of about 50 IU/kg to about 100 IU/kg of a chimeric factor IX (“FIX”) polypeptide comprising human FIX having an amino acid sequence identical to amino acids 1 to 415 of SEQ ID NO:2 and an FcRn binding partner (“FcRn BP”) at a dosing interval of about 10 days to about 14 days between two doses, wherein the FcRn BP is human albumin, wherein the administration treats the human subject by reducing the severity of a bleeding episode.
10. The method of claim 9 , wherein the chimeric FIX polypeptide further comprises a linker joining the FIX and the human albumin.
11. The method of claim 10 , wherein the linker joins the FIX to the N-terminal end of the human albumin.
12. The method of claim 11 , wherein the dosing interval is 14 days and each of the multiple doses is 50 IU/kg to 100 IU/kg.
13. The method of claim 9 , wherein the subject exhibits the plasma FIX activity above 1 IU/dL during the dosing interval as measured by a one stage clotting assay that determines activated partial thromboplastin time.
14. The method of claim 13 , wherein the chimeric FIX polypeptide further comprises a linker joining the FIX and the human albumin.
15. The method of claim 14 , wherein the linker joins the FIX to the N-terminal end of the human albumin.
16. The method of claim 15 , wherein the dosing interval is 14 days and each of the multiple doses is 50 IU/kg to 100 IU/kg.