Factor VIII-Fc chimeric and hybrid polypeptides, and methods of use thereof
The present invention provides methods of administering Factor VIII; methods of administering chimeric and hybrid polypeptides comprising Factor VIII; chimeric and hybrid polypeptides comprising Factor VIII; 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 maintaining homeostasis in a human subject in need of a surgery comprising administering to the subject multiple doses of about 10 IU/kg to about 50 IU/kg of a long-acting Factor VIII (“FVIII”) polypeptide at a dosing interval of 12 hours or longer between two doses,
wherein the long-acting FVIII polypeptide is a FVIIIFc monomer dimer hybrid comprising a FVIII portion and two Fc portions, wherein one of the Fc portions is fused to the C-terminus of the light chain of the FVIII portion.
2. The method of claim 1 , wherein a trough level of plasma Factor VIII:C in the subject after the administration is maintained above 3 IU/dl.
3. The method of claim 1 , wherein the administration prevents a bleeding episode in the subject.
4. The method of claim 1 , wherein the subject is in need of surgical prophylaxis, peri-operative management, or treatment for surgery.
5. The method of claim 1 , wherein the surgery is minor surgery, major surgery, tooth extraction, tonsillectomy, inguinal herniotomy, synovectomy, total knee replacement, craniotomy, osteosynthesis, trauma surgery, intracranial surgery, intra-abdominal surgery, intrathoracic surgery, or joint replacement surgery.
6. The method of claim 1 , wherein the surgery is an emergency surgery.
7. The method of claim 1 , wherein each of the doses is about 10 IU/kg, about 20 IU/kg, about 30 IU/kg, about 40 IU/kg, or about 50 IU/kg.
8. The method of claim 1 , wherein the dosing interval is 12 hours to 24 hours, 24 hours to 48 hours, or 48 hours to 72 hours.
9. The method of claim 1 , wherein the dosing interval is 12 hours to 24 hours.
10. The method of claim 1 , wherein the long-acting FVIII polypeptide is pegylated.
11. The method of claim 1 , wherein the FVIII portion comprises full-length FVIII, mature FVIII, or FVIII with a full or partial deletion of the B domain.
12. The method of claim 1 , wherein a mean clearance (CL) (activity) in the subject is about 2.33±1.08 mL/hour/kg or less.
13. The method of claim 1 , wherein a mean residence time (MRT) (activity) in the subject is about 1.5 fold longer than the mean MRT of a polypeptide consisting of said FVIII portion.
14. The method of claim 1 , wherein a T½ (activity) in the subject is about 1.5 fold longer than the mean T½ (activity) of a polypeptide consisting of said FVIII portion.
15. The method of claim 1 , wherein a mean incremental recovery (K value) in the subject is about 90% of the mean incremental recovery of a polypeptide consisting of said FVIII portion.
16. The method of claim 1 , wherein a mean Vss (activity) in the subject is about 37.7 to 79.4 mL/kg.
17. The method of claim 1 , wherein a mean AUC/dose (activity) in the subject is about 19.2*h/dL per IU/kg to 81.7 IU*h/dL per IU/kg.
18. The method of claim 1 , wherein the dosing interval is 24 hours to 72 hours.
19. The method of claim 1 , wherein the dosing interval is 24 hours to 48 hours.
20. A method of maintaining homeostasis in a human subject in need of surgical prophylaxis, peri-operative management, or treatment of surgery comprising administering to the subject multiple doses of about 35 IU/kg to about 50 RI/kg of a long-acting Factor VIII (“FVIII”) polypeptide at a dosing interval of 12 hours to 24 hours,
wherein the long-acting FVIII polypeptide is a FVIIIFc monomer dimer hybrid comprising a FVIII portion and two Fe portions, and wherein one of the Fe portions is fused to the C-terminus of the light chain of the FVIII portion.
21. A method of maintaining homeostasis in a human subject in need of surgical prophylaxis, peri-operative management, or treatment of surgery comprising administering to the subject multiple doses of about 35 IU/kg to about 50 IU/kg of a long-acting Factor VIII (“FVIII”) polypeptide at a dosing interval of 12 hours to 24 hours,
wherein the long-acting FVIII polypeptide is a FVIIIFc monomer dimer hybrid comprising a FVIII portion and two Fc portions, wherein one of the Fe portions is fused to the C-terminus of the light chain of the FVIII portion, and
wherein a trough level of plasma Factor VIII:C in the subject is maintained above 3 IU/dl between the administration of the doses.