Polymer von Willebrand factor-conjugates
View Patent ↗The present invention relates to a proteinaceous construct (also designated as polymer-VWF-conjugate) comprising plasmatic and/or recombinant von Willebrand factor (VWF), said VWF being bound to at least one physiologically acceptable polymer molecule, as well as to a complex between said proteinaceous construct and at least one factor VIII (FVIII) protein. The physiologically acceptable polymer molecule can be, for instance, polyethylene glycol (PEG) or polysialic acid (PSA). Further the present invention relates to methods for prolonging the in vivo-half-life of VWF or FVIII in the blood of a mammal having a bleeding disorder associated with functional defects of or deficiencies of at least one of FVIII or VWF.
1. A proteinaceous molecule comprising:
(a) a VWF molecule selected from the group consisting of plasmatic von Willebrand factor (VWF), recombinant VWF, a precursor, subunit or fragment of VWF having a biological activity of VWF as determined in a ristocetin cofactor assay or a collagen binding assay, and dimers and multimers thereof; and
(b) at least one physiologically acceptable polymer molecule bound to said VWF molecule;
said proteinaceous molecule having the capability of binding at least one factor VIII (FVIII) molecule, wherein the in vivo half-life of said proteinaceous molecule is increased as compared to the in vivo half-life of a VWF molecule,
and the in vivo half-life of said FVIII molecule bound to said proteinaceous molecule is increased as compared to the in vivo half-life of a FVIII molecule bound to VWF not linked to at least one physiologically acceptable polymer molecule.
2. The proteinaceous molecule of claim 1 wherein the in vivo half-life of said proteinaceous molecule is increased by at least a factor of about 1.5 as compared to the in vivo half-life of a VWF molecule.
3. The proteinaceous molecule of claim 1 , wherein said at least one physiologically acceptable polymer molecule is bound to a carbohydrate residue of said VWF molecule.
4. The proteinaceous molecule of claim 1 , wherein said at least one physiologically acceptable polymer molecule is bound to a lysine residue of said VWF molecule.
5. The proteinaceous molecule of claim 1 , wherein said physiologically acceptable polymer molecule is selected from the group consisting of poly(alkylene glycol), poly(propylene glycol), copolymers of ethylene glycol and propylene glycol, poly(oxyethylated polyol), poly(olefinic alcohol), poly(vinylpyrrolidone), poly(hydroxyalkylmethacrylamide), poly(hydroxyalkylmethacrylate), poly(saccharides), poly(α-hydroxy acid), poly(vinyl alcohol), polyphosphasphazene, polyoxazoline, and poly(N-acryloylmorpholine).
6. The proteinaceous molecule of claim 1 , wherein said physiologically acceptable polymer molecule is polyethylene glycol (PEG) or a derivative thereof.
7. The proteinaceous molecule of claim 1 , wherein said physiologically acceptable polymer molecule is polysialic acid (PSA) or a derivative thereof.
8. The proteinaceous molecule of claim 1 wherein the in vivo half-life of said FVIII molecule, when bound to said proteinaceous molecule, is increased by at least a factor of about 1.5 as compared to the in vivo half-life of a FVIII molecule bound to VWF not linked to at least one physiologically acceptable polymer molecule.
9. The proteinaceous molecule of claim 1 wherein said VWF molecule is a recombinant product.
10. A complex comprising the proteinaceous molecule of claim 1 and at least one FVIII molecule.
11. The complex of claim 10 , wherein the FVIII molecule is a recombinant product.
12. The complex of claim 10 wherein the in vivo half-life of said complex is increased by a factor of at least about 1.5 as compared to the in vivo half-life of a FVIII bound to a VWF molecule.
13. A method for prolonging the in vivo half-life of FVIII in the blood of a mammal having a bleeding disorder associated with a functional defect of or a deficiency of at least one of FVIII and VWF, comprising the steps of: (a) administering a first dose of at least one proteinaceous molecule of claim 1 to said mammal; and (b) administering a first dose of at least one FVIII molecule to said mammal.
14. The method of claim 13 wherein the FVIII molecule is not conjugated to a polymer.
15. A method for prolonging the in vivo half-life of FVIII in the blood of a mammal having a bleeding disorder associated with a functional defect of or a deficiency of at least one of FVIII and VWF, comprising the steps of: (a) providing at least one proteinaceous molecule of claim 1 ; (b) providing at least one FVIII molecule; (c) forming a complex between said proteinaceous molecule and said FVIII molecule; and (d) administering the complex of step (c) to said mammal.
16. The method of claim 15 wherein the FVIII molecule is not conjugated to a polymer.
17. A method for prolonging the in vivo half-life of endogenous FVIII in the blood of a mammal having a bleeding disorder associated with a functional defect of or a deficiency of at least one of FVIII and VWF, comprising administering a first dose of at least one proteinaceous molecule of claim 1 to said mammal.
18. A method of treating a bleeding disorder associated with a functional defect of or a deficiency of at least one of FVIII and VWF in a mammal, comprising the steps of: (a) administering a first dose of at least one proteinaceous molecule of claim 1 to said mammal; and (b) administering a first dose of at least one FVIII molecule to said mammal.
19. A method of treating a bleeding disorder associated with a functional defect of or a deficiency of at least one of FVIII and VWF in a mammal, comprising the steps of: (a) providing at least one proteinaceous molecule of claim 1 ; (b) providing at least one FVIII molecule; (c) forming a complex between said proteinaceous molecule and said FVIII molecule; and (d) administering the complex of step (c) to said mammal.
20. A pharmaceutical composition comprising an effective amount of the proteinaceous molecule of claim 1 and one or more compounds selected from the group consisting of a pharmaceutically acceptable carrier, diluent, salt, buffer, and excipient.