IP Library Granted Patent US 7,625,866
Granted Patent B2
US 7,625,866 · App. 10/670,563 · Granted Dec 1, 2009

Concentrate of a factor VIII:C-containing von Willebrand factor and the process relating thereto

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Quick Facts
Patent No.
US 7,625,866
App. No.
10/670,563
Granted
Dec 1, 2009
Kind
B2
Abstract

The invention relates to a concentrate and a process for producing a factor VIII:C-containing von Willebrand factor by fractional precipitation from a liquid comprising factor VIII:C and von Willebrand factor, resulting in an increased content of high molecular weight multimers of von Willebrand factor and a ratio of the vWF:RCoF activity to vWF:Ag of greater than 1.

Claims (16)

1. A process for producing a concentrate of a factor VIII:C-containing von Willebrand factor (vWF/FVIII:C), comprising subjecting a liquid comprising factor VIII:C (FVIII:C) and von Willebrand factor (vWF) to a fractional precipitation using an effective amount of at least one of an alkali metal salt or an alkaline earth metal salt, and an amino acid chosen from glycine, α- or β-alanine, α- or β- or γ-aminobutyric acid, lysine, valine, asparagine, and glutamic acid, wherein the fractional concentration of the amino acid is from about 67 to about 110 g/l, such that the produced concentrate has an increased content of high molecular weight multimers of vWF, and a ratio of von Willebrand factor ristocetin cofactor activity (vWF:RCoF) to von Willebrand factor antigen (vWF:Ag) of greater than 1.

2. The process as claimed in claim 1 wherein the amino acid is glycine.

3. The process as claimed in claim 1 wherein the alkali metal salt is NaCl.

4. The process as claimed in claim 1 further comprising:

stabilizing the concentrate product produced during said process with at least one of sucrose, glycine, calcium ions, and albumin; and

pasteurizing said concentrate product produced during said process.

5. The process as claimed in claim 4 , wherein calcium ions are added to stabilize the concentrate product.

6. The process as claimed in claim 1 , further comprising prior to the fractional precipitation:

(a) mixing the liquid with an aluminum hydroxide suspension, stirring, and removing the prothrombin complex;

(b) precipitating fibrinogen with an amino acid chosen from glycine, α- or β-alanine, α-, β-, or γ-aminobutyric acid, lysine, valine, asparagine, and glutamic acid and removing said fibrinogen; and

(c) precipitating the vWF/FVIII:C complex using an alkali metal salt or an alkaline earth metal salt.

7. The process as claimed in claim 6 , wherein the liquid is human plasma, a plasma fraction, or genetically modified cell material.

8. The process as claimed in claim 7 , wherein the plasma fraction is cryoprecipitate.

9. The process as claimed in claim 6 , wherein the amino acid is glycine.

10. The process as claimed in claim 6 , wherein the alkali metal salt is NaCl.

11. The process as claimed in claim 1 , wherein the fractional concentration of the alkali metal or the alkaline earth metal salt is from 100 to 160 g/l.

Assignments (3)
CHANGE OF NAME Recorded Sep 10, 2007
From: ZLB BEHRING GMBH
To: CSL BEHRING GMBH
Reel/Frame 019840/0193 →
CHANGE OF NAME Recorded Nov 4, 2004
From: AVENTIS BEHRING GMBH
To: ZLB BEHRING GMBH
Reel/Frame 015338/0740 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 11, 2004
From: KUMPE, GERHARDT; JURASCHEK, MANFRED; MAYER, NATASCHA; SCHULTE, STEFAN; WORMSBACHER, WILFRIED
To: AVENTIS BEHRING GMBH
Reel/Frame 014974/0551 →