IP Library Granted Patent US 11,884,742
Granted Patent B2
US 11,884,742 · App. 16/591,418 · Granted Jan 30, 2024

Methods for treating conditions associated with MASP-2 dependent complement activation

Inventors: Hans-Wilhelm Schwaeble (Cambridge, GB); Clark E. Tedford (Poulsbo, WA); James B. Parent (Bainbridge Island, WA); Thomas Dudler (Bellevue, WA); Gregory A. Demopulos (Mercer Island, WA)
Assignees: Omeros Corporation; University of Leicester
C07K16/40A01N1/0205A61K39/395A61K39/3955A61K45/06A61K2039/505C07K2317/21C07K2317/24C07K2317/54C07K2317/55C07K2317/76C07K2317/92
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Quick Facts
Patent No.
US 11,884,742
App. No.
16/591,418
Granted
Jan 30, 2024
Kind
B2
Abstract

In one aspect, the invention provides methods of inhibiting the effects of MASP-2-dependent complement activation in a living subject. The methods comprise the step of administering, to a subject in need thereof, an amount of a MASP-2 inhibitory agent effective to inhibit MASP-2-dependent complement activation. In some embodiments, the MASP-2 inhibitory agent inhibits cellular injury associated with MASP-2-mediated alternative complement pathway activation, while leaving the classical (C1q-dependent) pathway component of the immune system intact. In another aspect, the invention provides compositions for inhibiting the effects of lectin-dependent complement activation, comprising a therapeutically effective amount of a MASP-2 inhibitory agent and a pharmaceutically acceptable carrier.

Claims (14)

1. A method of inhibiting adverse effects of transplantation in a subject that has undergone, is undergoing, or will undergo a liver transplant procedure comprising administering to the subject, or pretreating the liver to be transplanted with, a composition comprising a monoclonal MASP-2 inhibitory antibody, or antigen-binding fragment thereof, that specifically binds to a portion of SEQ ID NO:6 and inhibits MASP 2 dependent complement activation.

2. The method of claim 1 , wherein the monoclonal MASP-2 inhibitory antibody, or antigen-binding fragment thereof, specifically binds to a polypeptide comprising SEQ ID NO:6 with an affinity of at least 10 times greater than it binds to a different antigen in the complement system.

3. The method of claim 1 , wherein the monoclonal MASP-2 inhibitory antibody, or antigen-binding fragment thereof, selectively inhibits MASP-2 dependent complement activation while leaving C1q-dependent classical complement pathway activation functionally intact.

4. The method of claim 1 , wherein the monoclonal MASP-2 inhibitory antibody has reduced effector function.

5. The method of claim 1 , wherein the monoclonal MASP-2 inhibitory antibody or antigen-binding fragment thereof is recombinant, chimeric, humanized or human.

6. The method of claim 1 , wherein the organ transplant procedure is selected from the group consisting of organ allotransplantation or a tissue graft.

7. The method of claim 1 , wherein the subject has undergone, is undergoing, or will undergo a liver transplant.

8. The method of claim 1 , wherein the method prevents or reduces an inflammatory reaction resulting from said organ transplantation.

9. The method of claim 1 , wherein the composition is administered to the subject by at least one of intra-arterial, intravenous, intramuscular, or subcutaneous administration.

10. The method of claim 1 , wherein the method comprises pretreating the organ to be transplanted with the composition comprising the monoclonal MASP-2 inhibitory antibody, or antigen-binding fragment thereof, that specifically binds to a portion of SEQ ID NO:6 and selectively inhibits MASP 2 dependent complement activation without substantially inhibiting C1q-dependent complement activation.

11. The method of claim 1 , wherein the method comprises administering the composition to the subject prior to the transplant procedure.

12. The method of claim 1 , wherein the method comprises administering the composition to the subject during the transplant procedure.

13. The method of claim 1 , wherein the method comprises administering the composition to the subject during the acute period following the transplant procedure.

14. The method of claim 1 , wherein the method comprises administering the composition to the subject as a long term post-transplantation therapy.

Assignments (3)
RELEASE OF SECURITY INTEREST Recorded Nov 25, 2025
From: WILMINGTON SAVINGS FUND SOCIETY, FSB
To: OMEROS CORPORATION
Reel/Frame 073705/0970 →
CORRECTIVE ASSIGNMENT TO CORRECT THE CORRECT THE BOX TITLED"THIS DOCUMENT SERVES AS AN OATH/DECLARATION (37 CFR 1.63)" WAS ERRONEOUSLY CHECKED AND THIS BOX SHOULD NOT HAVE BEEN CHECKED, PREVIOUSLY RECORDED AT REEL: 67607 FRAME: 108. ASSIGNOR(S) HEREBY CONFIRMS THE SECURITY INTEREST. Recorded Dec 11, 2024
From: OMEROS CORPORATION
To: WILMINGTON SAVINGS FUND SOCIETY, FSB, AS COLLATERAL AGENT
Reel/Frame 069715/0719 →
SECURITY INTEREST Recorded Jun 3, 2024
From: OMEROS CORPORATION
To: WILMINGTON SAVINGS FUND SOCIETY, FSB, AS COLLATERAL AGENT
Reel/Frame 067607/0108 →
Continuity (10)
Continuation 14459656 · Aug 14, 2014
Continuation 13083441 · Apr 8, 2011
Continuation In Part 12896754 · Oct 1, 2010
Continuation 12561202 · Sep 16, 2009
Division 11645359 · Dec 22, 2006
Continuation In Part 11150883 · Jun 9, 2005
Provisional Application 61322722 · Apr 9, 2010
Provisional Application 60788876 · Apr 3, 2006
Provisional Application 60578847 · Jun 10, 2004
Related Publication 20200157245A1 · May 21, 2020