IP Library Granted Patent US 8,415,288
Granted Patent B2
US 8,415,288 · App. 13/271,107 · Granted Apr 9, 2013

Use of C1 inhibitor for the prevention of ischemia-reperfusion injury

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Quick Facts
Patent No.
US 8,415,288
App. No.
13/271,107
Granted
Apr 9, 2013
Kind
B2
Abstract

The present invention relates to the therapeutic and prophylactic use of C1 inhibitor for preventing, reducing and treating ischemia and reperfusion injury. The C1 inhibitor of the present invention is still therapeutically effective when administered after an ischemic period and reperfusion and therefore particularly useful for unforeseen occurrences of ischemic reperfusion such as e.g. a stroke.

Claims (13)

1. A method of preventing, reducing or treating injury from brain or cerebral ischemia or reperfusion thereof in a patient comprising administering to the patient a C1 inhibitor having a reduced level of terminal sialic acid residues compared to plasma derived human C1 inhibitor and a plasma half-life of less than 6 hours, whereby the C1 inhibitor is administered at least 1 hour after the onset of ischemia and/or at least ten minutes after reperfusion.

2. The method according to claim 1 , wherein the C1 inhibitor comprises a glycan that has a terminal residue selected from galactose, N-acetylgalactosamine, N-acetylglucosamine, mannose and fucose.

3. The method according to claim 1 , wherein the C1 inhibitor is obtained from a genetically engineered cell or organism.

4. The method according to claim 3 , wherein the C1 inhibitor is obtained from a transgenic non-human animal.

5. The method according to claim 4 , wherein the C1 inhibitor is obtained from the milk of said transgenic non-human animal.

6. The method according to claim 4 , wherein the transgenic non-human animal is a bovine or an animal of the order Lagomorpha, preferably a rabbit.

7. The method according to claim 1 , wherein the C1 inhibitor is used in an amount in the range of 50-2000 units per kg body weight.

8. The method according to claim 1 , wherein the C1 inhibitor is administered 1-18 hours after the onset of ischemia.

9. The method according to claim 1 , wherein the C1 inhibitor is administered in combination with a thrombolytic agent or after treatment with such agent.

10. The method according to claim 1 , wherein the patient has at least one unforeseen sudden or acute occurrence of ischemia and/or reperfusion injury.

11. The method according to claim 10 , wherein the C1 inhibitor administration prevents, reduces or treats at least one of ischemia and reperfusion injury after stroke or perinatal stroke in the patient.

12. The method according to claim 1 , wherein the patient has at least one foreseen occurrence of ischemia and/or reperfusion injury, preferably after organ transplantation.

13. The method of claim 1 , wherein the C1 inhibitor is administered at least 3 hours after the onset of ischemia.

Assignments (2)
RELEASE OF SECURITY INTEREST Recorded Jan 28, 2020
From: ORBIMED ROYALTY OPPORTUNITIES II, LP
To: PHARMING GROUP N.V.; PHARMING TECHNOLOGIES B.V.; PHARMING INTELLECTUAL PROPERTY B.V.; BROEKMAN INSTITUUT B.V.; PHARMING B.V.; PHARMING AMERICAS B.V.; PHARMING HEALTHCARE, INC.
Reel/Frame 051722/0304 →
AMENDED AND RESTATED INTELLECTUAL PROPERTY SECURITY AGREEMENT Recorded May 16, 2017
From: PHARMING INTELLECTUAL PROPERTY B.V.
To: ORBIMED ROYALTY OPPORTUNITIES II, LP
Reel/Frame 042481/0139 →