IP Library Granted Patent US 10,494,443
Granted Patent B2
US 10,494,443 · App. 15/341,729 · Granted Dec 3, 2019

LOX and LOXL2 inhibitors and uses thereof

Inventors: Victoria Smith (Burlingame, CA); Scott Ogg (San Francisco, CA); Peter Van Vlasselaer (Portola Valley, CA); Vivian E. Barry (Foster City, CA); Derek Marshall (San Francisco, CA); Alison Kay Holzer (Palo Alto, CA); Hector Rodriguez (Brisbane, CA); Miho Oyasu (San Mateo, CA); Scott Alan McCauley (San Francisco, CA); Carlos Aurelio Garcia (Foster City, CA); Donna Hiroko Tokuoka Biermann (San Mateo, CA)
Assignee: GILEAD BIOLOGICS, INC.
C07K16/40C12Q1/6886G01N33/57423G01N33/57438G01N33/57484A61K2039/505C07K2317/24C07K2317/30C07K2317/33C07K2317/34C07K2317/565C07K2317/76C07K2317/77C07K2317/92G01N2333/90633
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Quick Facts
Patent No.
US 10,494,443
App. No.
15/341,729
Granted
Dec 3, 2019
Kind
B2
Abstract

The present application relates to anti-LOX and anti-LOXL2 antibodies and their use in purification, diagnostic and therapeutic methods. Antibodies include monoclonal antibodies, humanized antibodies and functional fragments thereof. Anti-LOX and anti-LOXL2 antibodies can be used to identify and treat conditions such as a fibrotic condition, angiogenesis, or to prevent a transition from an epithelial cell state to a mesenchymal cell state.

Claims (22)

1. An isolated monoclonal antibody or antigen binding fragment thereof that specifically binds to a lysyl oxidase-like 2 (LOXL2) protein and comprises a heavy chain variable region comprising complementarity determining region (CDR)1, CDR2 and CDR3 comprising the amino acid sequences set forth as SEQ ID NOs: 41, 42, and 70, respectively, and a light chain variable region comprising CDR1, CDR2 and CDR3 comprising the amino acid sequences set forth as SEQ ID NOs: 57, 58, and 59, respectively.

2. The isolated monoclonal antibody or antigen binding fragment of claim 1 , wherein the antibody or antigen binding fragment inhibits the enzymatic activity of the LOXL2 protein.

3. The isolated monoclonal antibody or antigen binding fragment of claim 1 , wherein the antibody or antigen binding fragment is a non-competitive inhibitor of the LOXL2 protein.

4. The isolated monoclonal antibody or antigen binding fragment of claim 1 , wherein the antibody or antigen binding fragment inhibits LOXL2 binding to ECM proteins, cellular receptors, or integrins.

5. The isolated monoclonal antibody or antigen binding fragment of claim 1 , wherein the antibody or antigen binding fragment reduces or inhibits uptake or internalization of LOXL2 protein.

6. The isolated monoclonal antibody or antigen binding fragment of claim 1 , wherein the antibody or antigen binding fragment is humanized.

7. The isolated monoclonal antibody or antigen binding fragment of claim 1 , wherein the antibody or antigen binding fragment is labeled with a therapeutic agent.

8. The isolated monoclonal antibody or antigen binding fragment of claim 1 , wherein the antibody or antigen binding fragment is labeled with a detectable label.

9. The isolated monoclonal antibody or antigen binding fragment of claim 1 , wherein the antibody or antigen binding fragment binds to LOXL2 with a binding affinity of at least 2, 5, 10, 50, 100, 500, or 1000 times greater than the binding affinity to at least one of LOX, LOXL1, LOXL3, or LOX4 proteins.

10. The isolated monoclonal antibody or antigen binding fragment of claim 1 , wherein the antibody or antigen binding fragment inhibits LOXL2 biological activity.

11. The isolated monoclonal antibody or antigen binding fragment of claim 1 , wherein the antibody or antigen binding fragment reduces tumor growth.

12. The isolated monoclonal antibody or antigen binding fragment of claim 1 , wherein the antibody or antigen binding fragment reduces incidence of metastasis.

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

14. The isolated monoclonal antibody or antigen binding fragment of claim 1 , wherein the heavy chain variable region comprises the amino acid sequence set forth as SEQ ID NOs: 25, 26, 27, or 28.

15. The isolated monoclonal antibody or antigen binding fragment of claim 1 , wherein the heavy chain variable region comprises the amino acid sequence set forth as SEQ ID NO: 27.

16. The isolated monoclonal antibody or antigen binding fragment of claim 1 , wherein the light chain variable region comprises the amino acid sequence set forth as SEQ ID NOs: 30, 31, or 32.

17. The isolated monoclonal antibody or antigen binding fragment of claim 1 , wherein the light chain variable region comprises the amino acid sequence set forth as SEQ ID NO: 31.

18. The isolated monoclonal antibody or antigen binding fragment of claim 1 , wherein the heavy chain variable region comprises the amino acid sequence set forth as SEQ ID NO: 27 and the light chain variable region comprises the amino acid sequence set forth as SEQ ID NO: 31.

19. The isolated monoclonal antibody or antigen binding fragment of claim 1 , wherein the isolated antibody or antigen binding fragment thereof is a Fv, a scFv, a Fab or a F(ab′) 2 .

20. The pharmaceutical composition of claim 13 , further comprising a second therapeutic agent.

21. The pharmaceutical composition of claim 20 , wherein the second therapeutic agent is an antibody or an anti-fibrotic agent.

22. The pharmaceutical composition of claim 21 , wherein the anti-fibrotic agent is selected from the group consisting of ethylenediamine, hydrazine, phenylhydrazine, semicarbazide, urea, aminonitriles, beta-aminopropionitrile (BAPN), 2-nitroethylamine, unsaturated or saturated haloamines, 2-bromo-ethylamine, 2-chloroethylamine, 2-trifluoroethyl amine, 3-bromopropylamine, p-halobenzylamines, selenohomocysteine lactone, copper chelating agents, thiolamines, D-penicillamine, 2-amino-5-mercapto-5-methylhexanoic acid, D-2-amino-3-methyl-3-((2-acetamidoethyl)dithio)butanoic acid, p-2-amino-3-methyl-3-((2-aminoethyl)dithio)butanoic acid, sodium-4-((p-1-dimethyl-2-amino-2-carboxyethyl)dithio) butane sulphinate, 2-acetamidoethyl-2-acetamidoethanethiol sulphanate, and sodium-4-mercaptobutanesulphinate trihydrate.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 1, 2017
From: SMITH, VICTORIA; OGG, SCOTT; VAN VLASSELAER, PETER; BARRY, VIVIAN E.; MARSHALL, DEREK; HOLZER, ALISON KAY; RODRIGUEZ, HECTOR; OYASU, MIHO; MCCAULEY, SCOTT ALAN; GARCIA, CARLOS AURELIO; BIERMANN, DONNA HIROKO TOKUOKA
To: ARRESTO BIOSCIENCES, INC.
Reel/Frame 041149/0369 →
MERGER Recorded Feb 1, 2017
From: ARRESTO BIOSCIENCES, INC.
To: GILEAD BIOLOGICS, INC.
Reel/Frame 041149/0376 →
Continuity (9)
Division 14877655 · Oct 7, 2015
Continuation 13888293 · May 6, 2013
Division 12185050 · Aug 1, 2008
Provisional Application 60963249 · Aug 2, 2007
Provisional Application 60963214 · Aug 2, 2007
Provisional Application 60963282 · Aug 2, 2007
Provisional Application 60963246 · Aug 2, 2007
Provisional Application 60963248 · Aug 2, 2007
Related Publication 20170240649A1 · Aug 24, 2017