IP Library › Granted Patent US 9,771,418
Granted Patent B2
US 9,771,418 · App. 15/243,290 · Granted Sep 26, 2017

Methods for treating complement-associated disorders

Inventors: Russell P. Rother (Oklahoma City, OK); Camille Bedrosian (Woodbridge, CT); Stephen P. Squinto (Bethany, CT); Leonard Bell (Woodbridge, CT)
Assignee: Alexion Pharmaceuticals, Inc.
C07K16/18A61K9/0019A61K39/3955A61K45/06A61K38/00A61K2039/505A61K2039/54A61K2039/545C07K2317/24C07K2317/34
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Quick Facts
Patent No.
US 9,771,418
App. No.
15/243,290
Granted
Sep 26, 2017
Kind
B2
Abstract

The present disclosure relates to, inter alia, compositions containing an inhibitor of human complement and use of the compositions in methods for treating or preventing complement-associated disorders. In some embodiments, the inhibitor is chronically administered to patients. In some embodiments, the inhibitor is administered to a patient in an amount and with a frequency to maintain systemic complement inhibition and prevent breakthrough. In some embodiments, the compositions contain an antibody, or antigen-binding fragment thereof, that binds to a human complement component C5 protein or a fragment of the protein such as C5a or C5b.

Claims (7)

1. A method for treating antibody-mediated rejection (AMR) in a patient having a kidney transplant, the method comprising intravenously administering to the patient:

1200 mg of eculizumab less than 24 hours before or during the transplant operation and one post-operative dose of eculizumab within 24 hours of the transplant operation;

900 mg of eculizumab once a week for four weeks after the post-operative dose; and

1200 mg of eculizumab on week five after the post-operative dose and bi-weekly thereafter.

2. The method of claim 1 , wherein the eculizumab is administered to the patient in an amount and with a frequency to maintain at least 50 μg of eculizumab per milliliter of the patient's blood.

3. The method of claim 1 , wherein the eculizumab is administered to the patient in an amount and with a frequency to maintain at least 100 μg of eculizumab per milliliter of the patient's blood.

4. The method of claim 1 , wherein the eculizumab is administered to the patient in an amount and with a frequency to maintain a concentration of at least 0.7 molecules of eculizumab per every C5 molecule in the patient's blood.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 17, 2016
From: BEDROSIAN, CAMILLE; SQUINTO, STEPHEN P.; BELL, LEONARD
To: ALEXION PHARMACEUTICALS, INC.
Reel/Frame 040031/0490 →
Continuity (12)
Division 13128523
Provisional Application 61200640 · Dec 1, 2008
Provisional Application 61199562 · Nov 18, 2008
Provisional Application 61199563 · Nov 18, 2008
Provisional Application 61181788 · May 28, 2009
Provisional Application 61199569 · Nov 18, 2008
Provisional Application 61200635 · Dec 1, 2008
Provisional Application 61199764 · Nov 19, 2008
Provisional Application 61228047 · Jul 23, 2009
Provisional Application 61200634 · Dec 1, 2008
Provisional Application 61198803 · Nov 10, 2008
Related Publication 20160355579A1 · Dec 8, 2016