Treatment with factor VII-albumin fusion protein
The present invention encompasses albumin fusion proteins. Nucleic acid molecules encoding the albumin fusion proteins of the invention are also encompassed by the invention, as are vectors containing these nucleic acids, host cells transformed with these nucleic acids vectors, and methods of making the albumin fusion proteins of the invention and using these nucleic acids, vectors, and/or host cells. Additionally the present invention encompasses pharmaceutical compositions comprising albumin fusion proteins and methods of treating, preventing, or ameliorating diseases, disorders or conditions using albumin fusion proteins of the invention.
1. A method of treating a patient in need of a Factor VII polypeptide, comprising the step of administering an effective amount of an albumin fusion protein comprising a Factor VII polypeptide fused to an albumin polypeptide, wherein the albumin polypeptide has the ability to prolong the serum half-life of the fused Factor VII polypeptide compared to the unfused Factor VII polypeptide, wherein the fused Factor VII polypeptide has Factor VII coagulant activity, wherein the Factor VII polypeptide is fused at the N-terminus of the albumin polypeptide, and wherein the albumin polypeptide is selected from:
a) a full-length albumin;
b) a mature albumin;
c) a fragment of albumin;
d) a polypeptide consisting of an amino acid sequence at least 95% identical to SEQ ID NO:18; and
e) amino acids 1 to 387 of SEQ ID NO:18;
and wherein the Factor VII polypeptide is selected from:
i) a full-length Factor VII;
ii) an activated Factor VII (Factor VIIa);
iii) a fragment of Factor VII having a deletion that consists of 1-50 amino acid residues compared to mature Factor VII;
iv) a polypeptide consisting of an amino acid sequence at least 90% identical to the sequence of amino acids 39 (Ala) to 444 (Pro) of SEQ ID NO: 47; and
a mature Factor VII.
2. The method of claim 1 , wherein the administration comprises subcutaneous administration.
3. The method of claim 2 , wherein the subcutaneous administration comprises one or more injections.
4. The method of claim 2 , wherein the effective amount of the albumin fusion protein is in the range of 1 μg/kg/day to 10 mg/kg/day of patient body weight.
5. The method of claim 4 , wherein the effective amount of the albumin fusion protein is at least 0.01 mg/kg/day.
6. The method of claim 2 , wherein the albumin fusion protein is administered continuously.
7. The method of claim 2 , wherein the subcutaneous administration comprises between 1 and 4 injections per day.
8. The method of claim 6 , wherein the continuous administration comprises continuous subcutaneous infusions.
9. The method of claim 2 , wherein the subcutaneous administration uses a sustained-release system.
10. The method of claim 1 , wherein said fragment of Factor VII has a deletion that consists of 1-25 amino acid residues as compared to a mature Factor VII.
11. The method of claim 1 , wherein said fragment of Factor VII has a deletion that consists of 1-10 amino acid residues as compared to a mature Factor VII.
12. The method of claim 1 , wherein said Factor VII polypeptide is derived from a human Factor VII.
13. The method of claim 1 , wherein said Factor VII polypeptide is an activated Factor VII (Factor VIIa), and wherein said activated Factor VII (Factor VIIa) is a full length Factor VIIa, a fragment of full length Factor VIIa having a deletion that consists of 1-50 amino acid residues as compared to mature Factor VII, or a polypeptide consisting of an amino acid sequence at least 90% identical to amino acids 39 (Ala) to 444 (Pro) of SEQ ID NO: 47.
14. The method of claim 13 , wherein said fragment of full length Factor VIIa has a deletion that consists of 1-25 amino acid residues as compared to full length Factor VIIa.
15. The method of claim 13 , wherein said fragment of full length Factor VIIa has a deletion that consists of 1-10 amino acid residues as compared to full length Factor VIIa.
16. The method of claim 13 , wherein said activated Factor VII (Factor VIIa) is derived from a human Factor VIIa.