IP Library Granted Patent US 8,354,377
Granted Patent B2
US 8,354,377 · App. 12/812,684 · Granted Jan 15, 2013

Use of factor VIIa or factor VIIa equivalents for preventing or attenuating haemorrhage growth, and/or oedema generation following intracerebral haemorrhage (ICH) in a selected subpopulation of ICH patients

Inventors: Brett Skolnick (Philadelphia, PA); Nikolai Constantin Brun (Copenhagen N, DK); Kamilla Begtrup (Allerød, DK)
Assignee: Novo Nordisk Health Care AG
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Quick Facts
Patent No.
US 8,354,377
App. No.
12/812,684
Granted
Jan 15, 2013
Kind
B2
Abstract

The invention relates to a method for preventing or attenuating one or more complications of intracerebral haemorrhage (ICH), the method comprising: (i) selecting an ICH patient who exhibits one or more of the following characteristics: age≦70, baseline ICH volume≦60 mL, baseline IVH volume≦5 mL, and elapsed time since onset of symptoms of less than about 2.5 hours; and (ii) administering to said patient in need thereof an effective amount of a first coagulation agent comprising Factor VIIa or a Factor VIIa equivalent.

Claims (11)

1. A method for preventing or attenuating one or more complications of intracerebral haemorrhage (ICH) in an ICH patient, the method comprising:

(i) selecting an ICH patient who has the following characteristics: (i) Age≦70, (ii) baseline ICH volume≦60 mL, (iii) baseline intraventricular haemorrhage (IVH) volume≦5 mL, and (iv) elapsed time since onset of symptoms of less than about 2.5 hours;

(ii) administering to said patient in need thereof an effective amount of a first coagulation agent comprising Factor VIIa or a Factor VIIa equivalent; and

(iii) reducing growth of a haematatoma in said patient.

2. The method according to claim 1 , wherein said patient has experienced spontaneous or traumatic ICH.

3. The method according to claim 1 , wherein said effective amount comprises at least about 20 μg/kg of said Factor VIIa or Factor VIIa equivalent.

4. The method according to claim 3 , wherein the effective amount comprises at least about 80 μg/kg Factor VIIa or Factor VIIa equivalent.

5. The method according to claim 1 , further comprising administering to the patient a second coagulation agent, wherein the amounts of said first and second coagulation agents together are effective in said preventing or attenuating.

6. The method according to claim 5 , wherein said second coagulation agent is a coagulation factor.

7. The method according to claim 5 , wherein said second coagulation agent is an antifibrinolytic agent.

8. The method according to claim 1 , wherein said administering results in one or more of: reduction in the number of days an ICH patient is hospitalized following ICH and a reduction in the risk of death in an ICH patient.

Assignments (3)
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 030656/0865 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 8, 2010
From: SKOLNICK, BRETT; BRUN, NIKOLAI CONSTANTIN; BEGTRUP, KAMILLA
To: NOVO NORDISK HEALTHCARE AG
Reel/Frame 024950/0326 →
Priority Claims (2)
EP 08100633 · Jan 18, 2008 · regional
EP 08100916 · Jan 25, 2008 · regional
Continuity (2)
Provisional Application 61025387 · Feb 1, 2008
Related Publication 20110014179A1 · Jan 20, 2011