IP Library Granted Patent US 11,883,493
Granted Patent B2
US 11,883,493 · App. 17/241,628 · Granted Jan 30, 2024

Antibodies specifically binding to MASP-3 for the treatment of various diseases and disorders

Inventors: W. Jason Cummings (Bellevue, WA); Gregory A. Demopulos (Mercer Island, WA); Thomas Dudler (Bellevue, WA); Larry W. Tjoelker (Kirkland, WA); Christi L. Wood (Snohomish, WA); Munehisa Yabuki (Seattle, WA)
Assignee: OMEROS CORPORATION
A61K39/3955B82Y25/00C01F17/206C07K16/40C09K11/77C09K11/7728C12N9/6424C12Y304/21104H01F1/0054A61K39/00A61K2039/505A61K2039/54A61K2039/545C01P2002/54C01P2002/84C01P2004/64C07K2317/24C07K2317/33C07K2317/34C07K2317/56C07K2317/565C07K2317/734C07K2317/76C07K2317/90C07K2317/92
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 11,883,493
App. No.
17/241,628
Granted
Jan 30, 2024
Kind
B2
Abstract

The present invention relates to MASP-3 inhibitory antibodies and compositions comprising such antibodies for use in inhibiting the adverse effects of MASP-3 dependent complement activation.

Claims (19)

1. An isolated antibody, or antigen-binding fragment thereof, that binds to MASP-3 comprising a heavy chain variable region comprising an HC-CDR1, an HC-CDR2, and an HC-CDR3 and a light chain variable region comprising an LC-CDR1, an LC-CDR2, and an LC-CDR3, wherein:

i) the HC-CDR1 comprises SEQ ID NO:56, the HC-CDR2 comprises SEQ ID NO:58, the HC-CDR3 comprises SEQ ID NO:60 and wherein the LC-CDR1 comprises SEQ ID NO:142, SEQ ID NO:257, SEQ ID NO:258 or SEQ ID NO:259; wherein the LC-CDR2 comprises SEQ ID NO:144 and wherein the LC-CDR3 comprises SEQ ID NO:146; or

ii) the HC-CDR1 comprises SEQ ID NO:62, the HC-CDR2 comprises SEQ ID NO:63, SEQ ID NO:67 or SEQ ID NO:69, the HC-CDR3 comprises SEQ ID NO:65 and wherein the LC-CDR1 comprises SEQ ID NO:149, the LC-CDR2 comprises SEQ ID NO:144 and the LC-CDR3 comprises SEQ ID NO:146.

2. The antibody or antigen binding fragment thereof of claim 1 , wherein the antibody or antigen-binding fragment is selected from the group consisting of a humanized antibody, a chimeric antibody, a murine antibody, and an antigen-binding fragment of any of the foregoing.

3. The antibody or antigen-binding fragment thereof of claim 1 , wherein said antibody or antigen binding fragment thereof is selected from the group consisting of a single chain antibody, an ScFv, a Fab fragment, an Fab′ fragment, an F(ab′)2 fragment, a univalent antibody lacking a hinge region and a whole antibody.

4. The antibody or antigen-binding fragment thereof of claim 1 , further comprising an immunoglobulin constant region.

5. The antibody or antigen binding fragment thereof of claim 1 , wherein the antibody or antigen-binding fragment is humanized.

6. The antibody or antigen-binding fragment thereof of claim 1 , wherein said antibody binds to the serine protease domain of human MASP-3 with an affinity of less than 500 pM.

7. The antibody or antigen-binding fragment thereof of claim 1 , wherein said antibody inhibits alternative pathway activation in mammalian blood.

8. The antibody or antigen-binding fragment thereof of claim 1 , wherein the HC-CDR1 comprises SEQ ID NO:56, the HC-CDR2 comprises SEQ ID NO:58, the HC-CDR3 comprises SEQ ID NO:60 and wherein the LC-CDR1 comprises SEQ ID NO:142, SEQ ID NO:257, SEQ ID NO:258 or SEQ ID NO:259; wherein the LC-CDR2 comprises SEQ ID NO:144 and wherein the LC-CDR3 comprises SEQ ID NO:146.

9. The antibody or antigen-binding fragment thereof of claim 1 , wherein the HC-CDR1 comprises SEQ ID NO:62, the HC-CDR2 comprises SEQ ID NO:63, SEQ ID NO:67 or SEQ ID NO:69, the HC-CDR3 comprises SEQ ID NO:65 and wherein the LC-CDR1 comprises SEQ ID NO:149, the LC-CDR2 comprises SEQ ID NO:144 and the LC-CDR3 comprises SEQ ID NO:146.

10. A pharmaceutical composition comprising the antibody or antigen-binding fragment of claim 1 and a pharmaceutically acceptable excipient.

11. The antibody or antigen-binding fragment thereof of claim 8 , wherein the HC-CDR1 comprises SEQ ID NO:56, the HC-CDR2 comprises SEQ ID NO:58, and the HC-CDR3 comprises SEQ ID NO:60 and wherein the LC-CDR1 comprises SEQ ID NO:142, wherein the LC-CDR2 comprises SEQ ID NO:144 and wherein the LC-CDR3 comprises SEQ ID NO:146.

12. The antibody or antigen-binding fragment thereof of claim 8 , wherein the HC-CDR1 comprises SEQ ID NO:56, the HC-CDR2 comprises SEQ ID NO:58, and the HC-CDR3 comprises SEQ ID NO:60 and wherein the LC-CDR1 comprises SEQ ID NO:257, wherein the LC-CDR2 comprises SEQ ID NO:144 and wherein the LC-CDR3 comprises SEQ ID NO:146.

13. The antibody or antigen-binding fragment thereof of claim 8 , wherein the HC-CDR1 comprises SEQ ID NO:56, the HC-CDR2 comprises SEQ ID NO:58, and the HC-CDR3 comprises SEQ ID NO:60 and wherein the LC-CDR1 comprises SEQ ID NO:258, wherein the LC-CDR2 comprises SEQ ID NO:144 and wherein the LC-CDR3 comprises SEQ ID NO:146.

14. The antibody or antigen-binding fragment thereof of claim 8 , wherein the HC-CDR1 comprises SEQ ID NO:56, the HC-CDR2 comprises SEQ ID NO:58, and the HC-CDR3 comprises SEQ ID NO:60 and wherein the LC-CDR1 comprises SEQ ID NO:259, wherein the LC-CDR2 comprises SEQ ID NO:144 and wherein the LC-CDR3 comprises SEQ ID NO:146.

15. The antibody or antigen-binding fragment thereof of claim 9 , wherein the HC-CDR1 comprises SEQ ID NO:62, the HC-CDR2 comprises SEQ ID NO:63, and the HC-CDR3 comprises SEQ ID NO:65 and wherein the LC-CDR1 comprises SEQ ID NO:149, the LC-CDR2 comprises SEQ ID NO:144 and the LC-CDR3 comprises SEQ ID NO:146.

16. The antibody or antigen-binding fragment thereof of claim 9 , wherein the HC-CDR1 comprises SEQ ID NO:62, the HC-CDR2 comprises SEQ ID SEQ ID NO:67, and the HC-CDR3 comprises SEQ ID NO:65 and wherein the LC-CDR1 comprises SEQ ID NO:149, the LC-CDR2 comprises SEQ ID NO:144 and the LC-CDR3 comprises SEQ ID NO:146.

17. The antibody or antigen-binding fragment thereof of claim 9 , wherein the HC-CDR1 comprises SEQ ID NO:62, the HC-CDR2 comprises SEQ ID NO:69, and the HC-CDR3 comprises SEQ ID NO:65 and wherein the LC-CDR1 comprises SEQ ID NO:149, the LC-CDR2 comprises SEQ ID NO:144 and the LC-CDR3 comprises SEQ ID NO:146.

Assignments (4)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 9, 2025
From: OMEROS CORPORATION
To: NOVO NORDISK HEALTH CARE AG
Reel/Frame 073916/0555 →
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 (7)
Division 16909578 · Jun 23, 2020
Division 16837600 · Apr 1, 2020
Division 15665030 · Jul 31, 2017
Provisional Application 62478336 · Mar 29, 2017
Provisional Application 62419420 · Nov 8, 2016
Provisional Application 62369674 · Aug 1, 2016
Related Publication 20210275667A1 · Sep 9, 2021