IP Library Granted Patent US 7,459,534
Granted Patent B2
US 7,459,534 · App. 10/974,534 · Granted Dec 2, 2008

Inactivation resistant factor VIII

Assignee: The Regents of the University of Michigan
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Quick Facts
Patent No.
US 7,459,534
App. No.
10/974,534
Granted
Dec 2, 2008
Kind
B2
Abstract

The present invention provides novel purified and isolated nucleic acid sequences encoding procoagulant-active FVIII proteins. The nucleic acid sequences of the present invention encode amino acid sequences corresponding to known human FVIII sequences, wherein residue Phe309 is mutated. The nucleic acid sequences of the present invention also encode amino acid sequences corresponding to known human FVIII sequences, wherein the APC cleavage sites, Arg336 and Ile562, are mutated. The nucleic acid sequences of the present invention further encode amino acid sequences corresponding to known human FVIII sequences, wherein the B-domain is deleted, the von Willebrand factor binding site is deleted, a thrombin cleavage site is mutated and an amino acid sequence spacer is inserted between the A2- and A3-domains. Methods of producing the FVIII proteins of the invention, nucleotide sequences encoding such proteins, pharmaceutical compositions containing the nucleotide sequences or proteins, as well as methods of treating patients suffering from hemophilia, are also provided.

Claims (4)

1. A procoagulant-active FVIII protein comprising a human FVIII polypeptide that is modified, wherein the modification comprises a substitution of the Arg residue at position 336 with Ile, a substitution of the Arg residue at position 562 with Lys, and a substitution of Phe at position 309 with Ser, wherein said protein is APC resistant.

2. A pharmaceutical composition comprising an effective amount of the protein of claim 1 in admixture with a parenterally acceptable vehicle or excipient.

3. The procoagulant-active FVIII protein of claim 1 , further comprising a modification selected from the group consisting of a substitution of Leu at position 308 with Glu and a substitution of Gln at position 305 with Lys.

4. A pharmaceutical composition comprising an effective amount of the protein of claim 3 in admixture with a parenterally acceptable vehicle or excipient.

Assignments (4)
CONFIRMATORY LICENSE Recorded May 6, 2010
From: UNIVERSITY OF MICHIGAN
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 024344/0542 →
CONFIRMATORY LICENSE Recorded Nov 13, 2009
From: UNIVERSITY OF MICHIGAN
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 023510/0332 →
CONFIRMATORY LICENSE Recorded Sep 22, 2008
From: UNIVERSITY OF MICHIGAN
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 021562/0993 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 3, 2005
From: KAUFMAN, RANDAL J.; PIPE, STEVEN W.; AMANO, KAGEHIRO
To: REGENTS OF THE UNIVERSITY OF MICHIGAN, THE
Reel/Frame 016849/0402 →
Continuity (6)
Continuation 0981909800 · Apr 11, 2001
Continuation 0898003800 · Nov 26, 1997
Continuation In Part PCTUS970656300 · Apr 24, 1997
Provisional Application 6001611700 · Apr 24, 1996
Provisional Application 6001778500 · May 15, 1996
Related Publication 20060014683A1 · Jan 19, 2006