IP Library Patent Application 10946378
Patent Application
App. No. 10/946,378

Biologically stable liquid composition of FVIII, of vWF or of FVIII/vWF complex of human origin

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Patent No.
US None
App. No.
10/946,378
Abstract

Biologically stable liquid composition of FVIII, of vWF or of FVIII/vWF complex of human origin. The composition comprises a concentrate of FVIII, of vWF or of FVIII/vWF complex of human origin with a chelating agent for metals, a specific ligand and preferably a protease inhibitor.

Claims (11)

1 . Biologically stable liquid composition of FVIII or of vWF or of FVIII/vWF complex of human origin, characterised in that it comprises a concentrate of FVIII or of vWF or of FVIII/vWF complex of human origin with a chelating agent for metals, a specific ligand and preferably a protease inhibitor.

2 . Biologically stable liquid composition of FVIII or of vWF or of FVIII/vWF complex of human origin according to claim 1 , characterised in that the chelating agent for metals is used at a concentration of 2-100 mmol/l of the concentrate.

3 . Biologically stable liquid composition of FVIII or of vWF or of FVIII/vWF complex of human origin according to claim 1 , characterised in that the chelating agent for metals is EDTA.

4 . Biologically stable liquid composition of FVIII or of vWF or of FVIII/vWF complex of human origin according to claim 1 , characterised in that the chelating agent for metals is EDTACaNa 2 (sodium and calcium salt of EDTA).

5 . Biologically stable liquid composition of FVIII or of vWF or of FVIII/vWF complex of human origin, according to claim 1 , characterised in that the ligand is included at a concentration of 0.1-10 U/ml of the concentrate.

6 . Biologically stable liquid composition of FVIII or of vWF or of FVIII/vWF complex of human origin according to claim 1 , characterised in that the ligand is heparin.

7 . Biologically stable liquid composition of FVIII or of vWF or of FVIII/vWF complex of human origin according to claim 1 , characterised in that the ligand is sodium heparin.

8 . Biologically stable liquid composition of FVIII or of vWF or of FVIII/vWF complex of human origin according to claim 1 , characterised in that the protease inhibitor is present at a concentration greater than 0.01 IU/IU FVIII.

9 . Biologically stable liquid composition of FVIII or of vWF or of FVIII/vWF complex of human origin according to claim 8 , characterised in that the protease inhibitor is present at a concentration of 0.01-1 IU/IU FVIII.

10 . Biologically stable liquid composition of FVIII or of vWF or of FVIII/vWF complex of human origin according to claim 1 , characterised in that the protease inhibitor is a serine protease inhibitor (serpin).

11 . Biologically stable liquid composition of FVIII or of vWF or of FVIII/vWF complex of human origin according to claim 10 , characterised in that the serine protease inhibitor is antithrombin.

Assignments (3)
CONFIRMATORY LICENSE Recorded Jul 20, 2023
From: NORTH CAROLINA STATE UNIVERSITY RALEIGH
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 064354/0051 →
CHANGE OF NAME Recorded Dec 6, 2005
From: PROBITAS PHARMA, S.A.
To: GRIFOLS, S.A.
Reel/Frame 017089/0345 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 21, 2004
From: GAMON, SALVADOR GRANCHA; NIETO, JUAN IGNACIO JORQUERA; DEBART, PERE RISTOL; RIERA, MARTA MASSOT
To: PROBITAS PHARMA, S.A.
Reel/Frame 015824/0272 →