IP Library Granted Patent US 7,419,949
Granted Patent B2
US 7,419,949 · App. 10/196,902 · Granted Sep 2, 2008

Single-dose administration of factor VIIa

Assignee: Novo Noridsk HealthCare A/G
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Quick Facts
Patent No.
US 7,419,949
App. No.
10/196,902
Granted
Sep 2, 2008
Kind
B2
Abstract

The present invention provides methods for preventing and/or treating bleeding episodes by administering a single dose of Factor VIIa or a Factor VIIa equivalent. Preferably, the single dose comprises between about 150 and about 500 μg/kg Factor VIIa or Factor VIIa equivalent.

Claims (12)

1. A method for treating a bleeding episode in a human subject in need of such treatment, said method comprising administering intravenously to said human subject purified Factor VIIa, wherein said administering is in a single dose and said dose comprises a single-dose-effective amount of said Factor VIIa, wherein said single-dose-effective amount comprises between 250 and 500 μg/kg Factor VIIa and wherein, subsequent to said administration, no further Factor VIIa is administered to said subject for a period of at least 4 hours.

2. A method as defined in claim 1 , wherein said period is at least 24 hours.

3. A method as defined in claim 1 , wherein said single dose is administered over a period of less than 5 minutes.

4. A method as defined in claim 1 , wherein said single-dose-effective amount comprises between 300 and 500 μg/kg Factor VIIa.

5. A method as defined in claim 1 , further comprising administering, in said single dose, or substantially simultaneously with said single dose, a second coagulant agent.

6. A method as defined in claim 5 , wherein said second coagulant agent is selected from the group consisting of Factor VIII, Factor IX, and Factor XIII.

7. A method as defined in claim 1 , further comprising administering an anticoagulant, wherein said anticoagulant is administered in said single dose, or substantially simultaneously with said single dose.

8. A method for treating a bleeding episode, said method comprising administering intravenously to a human subject in need of such treatment (i) a first amount of purified Factor VIIa and (ii) a second amount of second coagulant agent, wherein said first amount consists of between 250 and 500 μg/kg Factor VIIa and wherein said first and second amounts together comprise an aggregate effective amount for treating said bleeding and said aggregate effective amount is administered in a single dose.

9. A method for treating a bleeding episode, said method comprising administering intravenously to a human subject in need of such treatment an effective amount for treating said bleeding of purified human Factor VIIa, wherein:

(i) said effective amount is administered in a single dose over a period of less than 5 minutes;

(ii) said effective amount comprises between 300 and 500 μg/kg human Factor VIIa; and

(iii) subsequent to said administration, no further Factor VIIa is administered to said subject for a period of at least 1 hour.

Assignments (4)
CHANGE OF ADDRESS OF ASSIGNEE Recorded Nov 15, 2021
From: NOVO NORDISK HEALTHCARE A/G
To: NOVO NORDISK HEALTHCARE AG
Reel/Frame 058122/0546 →
CHANGE OF ADDRESS Recorded Jun 19, 2013
From: NOVO NORDISK HEALTHCARE A/G
To: NOVO NORDISK HEALTHCARE AG
Reel/Frame 030653/0226 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 14, 2005
From: NOVO NORDISK A/S
To: NOVO NORDISK HEALTHCARE A/G
Reel/Frame 015712/0930 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 20, 2002
From: HEDNER, ULLA
To: NOVO NORDISK A/S
Reel/Frame 013518/0594 →
Continuity (2)
Provisional Application 6030572000 · Jul 16, 2001
Related Publication 20030054018A1 · Mar 20, 2003