IP Library › Granted Patent US 10,202,448
Granted Patent B2
US 10,202,448 · App. 15/228,254 · Granted Feb 12, 2019

Anti-IL-23 antibodies

Inventors: Rachel Rebecca Barrett (Bethel, CT); Keith A. Canada (Woodbury, CT); Katrina Mary Catron (Middlebury, CT); Robert Copenhaver (Portland, OR); Lee Edward Frego (Hopewell Junction, NY); Ernest Lee Raymond (New Milford, CT); Sanjaya Singh (Sandy Hook, CT); Xiangyang Zhu (Ridgefield, CT)
Assignee: Boehringer Ingelheim International GmbH
C07K16/244C12N15/113A61K2039/505C07K2317/24C07K2317/34C07K2317/565C07K2317/76C07K2317/92C07K2317/94
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Quick Facts
Patent No.
US 10,202,448
App. No.
15/228,254
Granted
Feb 12, 2019
Kind
B2
Abstract

The present invention relates to anti-IL-23p19 binding compounds, in particular new humanized anti-IL-23p19 antibodies and therapeutic and diagnostic methods and compositions for using the same.

Claims (11)

1. A method for treating a subject having a disorder associated with increased interleukin 23 (IL-23) expression comprising administering to the subject an anti-IL-23p19 antibody or antigen-binding fragment or a pharmaceutical composition comprising an anti-IL-23p19 antibody or antigen-binding fragment and a pharmaceutically acceptable carrier, which antibody or antigen-binding fragment binds to human IL-23, wherein the antibody or antigen-binding fragment thereof comprises: a) a light chain variable region comprising the amino acid sequence of SEQ ID NO:19 (CDR1-L); the amino acid sequence of SEQ ID NO:20 (CDR2-L); and the amino acid sequence of SEQ NO:21 (CDR3-L); and b) a heavy chain variable region comprising the amino acid sequence of SEQ ID NO: 63, 66, 67 or 68 (CDR1-H); the amino acid sequence of SEQ ID NO:64 (CDR2-H); and the amino acid sequence of SEQ ID NO:65 (CDR3-H).

2. The method of claim 1 , wherein the anti-IL-23p19 antibody or antigen-binding fragment comprises a light chain variable region comprising an amino acid sequence of SEQ ID NO: 160 and a heavy chain variable region comprising an amino acid sequence of SEQ ID NO: 166.

3. The method of claim 1 , wherein the anti-IL-23p19 antibody or antigen-binding fragment comprises a light chain comprising an amino acid sequence of SEQ ID NO: 174 and a heavy chain comprising an amino acid sequence of SEQ ID NO: 176.

4. A method for treating an inflammatory disease, an autoimmune disease, or cancer comprising administering to a subject in need thereof an effective amount of an anti-IL-23p19 antibody or antigen-binding fragment or a pharmaceutical composition comprising an anti-IL-23p19 antibody or antigen-binding fragment and a pharmaceutically acceptable carrier, wherein the antibody or antigen-binding fragment thereof comprises: a) a light chain variable region comprising the amino acid sequence of SEQ ID NO:19 (CDR1-L); the amino acid sequence of SEQ ID NO:20 (CDR2-L); and the amino acid sequence of SEQ ID NO:21 (CDR3-L); and b) a heavy chain variable region comprising the amino acid sequence of SEQ ID NO: 63, 66, 67 or 68 (CDR1-H); the amino acid sequence of SEQ ID NO:64 (CDR2-H); and the amino acid sequence of SEQ ID NO:65 (CDR3-H).

5. The method of claim 4 , wherein the anti-IL-23p19 antibody or antigen-binding fragment comprises a light chain variable region comprising an amino acid sequence of SEQ ID NO: 160 and a heavy chain variable region comprising an amino acid sequence of SEQ ID NO: 166.

6. The method of claim 4 , wherein the anti-IL-23p19 antibody or antigen-binding fragment comprises a light chain comprising an amino acid sequence of SEQ ID NO: 174 and a heavy chain comprising an amino acid sequence of SEQ ID NO: 176.

7. A method for inhibiting the binding of IL-23 to the IL-23 receptor on a mammalian cell, comprising administering to the cell an anti-IL-23p19 antibody or antigen-binding fragment, whereby signaling mediated by the IL-23 receptor is inhibited, wherein the antibody or antigen-binding fragment thereof comprises:

a) a light chain variable region comprising the amino acid sequence of SEQ ID NO:19 (CDR1-L); the amino acid sequence of SEQ ID NO:20 (CDR2-L); and the amino acid sequence of SEQ ID NO:21 (CDR3-L); and

b) a heavy chain variable region comprising the amino acid sequence of SEQ ID NO: 63, 66, 67 or 68 (CDR1-H); the amino acid sequence of SEQ ID NO:64 (CDR2-H); and the amino acid sequence of SEQ ID NO:65 (CDR3-H).

8. The method of claim 7 , wherein the anti-IL-23p19 antibody or antigen-binding fragment comprises a light chain variable region comprising an amino acid sequence of SEQ ID NO: 160 and a heavy chain variable region comprising an amino acid sequence of SEQ ID NO: 166.

9. The method of claim 7 , wherein the anti-IL-23p19 antibody or antigen-binding fragment comprises a light chain comprising an amino acid sequence of SEQ ID NO: 174 and a heavy chain comprising an amino acid sequence of SEQ ID NO: 176.

Continuity (7)
Division 14302986 · Jun 12, 2014
Division 13287208 · Nov 2, 2011
Provisional Application 61448785 · Mar 3, 2011
Provisional Application 61412594 · Nov 11, 2010
Provisional Application 61411953 · Nov 10, 2010
Provisional Application 61410158 · Nov 4, 2010
Related Publication 20160333091A1 · Nov 17, 2016
Cited By (5)
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