IP Library › Granted Patent US 10,350,276
Granted Patent B2
US 10,350,276 · App. 16/214,996 · Granted Jul 16, 2019

Single dose administration of factor VIIa

Inventor: Ulla Hedner (Malmoe, SE)
Assignee: Novo Nordisk HealthCare AG
A61K38/4846A61K9/0019A61K38/37A61K38/45A61K45/06C12Y304/21021
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Quick Facts
Patent No.
US 10,350,276
App. No.
16/214,996
Granted
Jul 16, 2019
Kind
B2
Abstract

The present invention provides methods for preventing and/or treating bleeding episodes by administering a single dose of a Factor VIIa equivalent. Preferably, the single dose comprises between about 150 and about 500 ug/kg 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 200 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 , further comprising administering, in said single dose, or substantially simultaneously with said single dose, a second coagulant agent.

5. A method as defined in claim 4 , wherein said second coagulant agent is selected from the group consisting of Factor VIII, Factor IX, and Factor XIII.

6. 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.

7. 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 200 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, and wherein, subsequent to said administration, no further Factor VIIa is administered to said subject for a period of at least 4 hours.

8. 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 200 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 4 hours,

wherein said human subject suffers from a bleeding disorder.

Continuity (9)
Continuation 15903547 · Feb 23, 2018
Continuation 15634153 · Jun 27, 2017
Continuation 15249598 · Aug 29, 2016
Continuation 14973837 · Dec 18, 2015
Continuation 14683392 · Apr 10, 2015
Continuation 12127917 · May 28, 2008
Continuation 10196902 · Jul 16, 2002
Provisional Application 60305720 · Jul 16, 2001
Related Publication 20190091303A1 · Mar 28, 2019