IP Library Granted Patent US 8,404,813
Granted Patent B2
US 8,404,813 · App. 13/031,544 · Granted Mar 26, 2013

Engineered anti-IL-23P19 antibodies

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Quick Facts
Patent No.
US 8,404,813
App. No.
13/031,544
Granted
Mar 26, 2013
Kind
B2
Abstract

Engineered antibodies to human IL-23p19 are provided, as well as uses thereof, e.g. in treatment of inflammatory, autoimmune, and proliferative disorders.

Claims (47)

1. A purified binding compound that binds to human IL-23, comprising:

a) an antibody light chain variable domain, or antigen binding fragment thereof, comprising CDRL1, CDRL2 and CDRL3, wherein:

CDRL1 comprises the sequence of SEQ ID NO: 36;

CDRL2 comprises the sequence of SEQ ID NO: 41; and

CDRL3 comprises the sequence of SEQ ID NO: 46; and

b) an antibody heavy chain variable domain, or antigen binding fragment thereof, comprising CDRH1, CDRH2 and CDRH3, wherein:

CDRH1 comprises the sequence of SEQ ID NO: 19;

CDRH2 comprises a sequence selected from the group consisting of SEQ ID NOs: 24-26; and

CDRH3 comprises the sequence of SEQ ID NO: 31.

2. The binding compound of claim 1 wherein CDRL2 comprises the sequence of SEQ ID NO: 24.

3. The binding compound of claim 1 wherein CDRL2 comprises the sequence of SEQ ID NO: 25.

4. The binding compound of claim 1 wherein CDRL2 comprises the sequence of SEQ ID NO: 26.

5. The binding compound of claim 2 comprising:

a) an antibody light chain variable domain comprising residues 1-108 of SEQ ID NO: 14; and

b) an antibody heavy chain variable domain comprising residues 1-116 of SEQ ID NO: 6.

6. The binding compound of claim 3 comprising:

a) an antibody light chain variable domain comprising residues 1-108 of SEQ ID NO: 14; and

b) an antibody heavy chain variable domain comprising residues 1-116 of SEQ ID NO: 7.

7. The binding compound of claim 4 comprising:

a) an antibody light chain variable domain comprising residues 1-108 of SEQ ID NO: 14; and

b) an antibody heavy chain variable domain comprising residues 1-116 of SEQ ID NO: 8.

8. The binding compound of claim 5 comprising an antibody light chain and an antibody heavy chain, wherein:

a) the antibody light chain comprises the sequence of SEQ ID NO: 14; and

b) the antibody heavy chain comprises the sequence of SEQ ID NO: 6.

9. The binding compound of claim 6 comprising an antibody light chain and an antibody heavy chain, wherein:

a) the antibody light chain comprises the sequence of SEQ ID NO: 14; and

b) the antibody heavy chain comprises the sequence of SEQ ID NO: 7.

10. The binding compound of claim 7 comprising an antibody light chain and an antibody heavy chain, wherein:

a) the antibody light chain comprises the sequence of SEQ ID NO: 14; and

b) the antibody heavy chain comprises the sequence of SEQ ID NO: 8.

11. The binding compound of claim 1 , further comprising a heavy chain constant region comprising a γ1 human heavy chain constant region.

12. The binding compound of claim 1 , further comprising a heavy chain constant region comprising a γ4 human heavy chain constant region.

13. The binding compound of claim 2 , wherein the binding compound is an antibody fragment selected from the group consisting of Fab, Fab′, Fab′-SH, Fv, scFv, F(ab′) 2 , and a diabody.

14. The binding compound of claim 3 , wherein the binding compound is an antibody fragment selected from the group consisting of Fab, Fab′, Fab′-SH, Fv, scFv, F(ab′) 2 , and a diabody.

15. The binding compound of claim 4 , wherein the binding compound is an antibody fragment selected from the group consisting of Fab, Fab′, Fab′-SH, Fv, scFv, F(ab′) 2 ,and a diabody.

16. The binding compound of claim 5 , wherein the binding compound is an antibody fragment selected from the group consisting of Fab, Fab′, Fab′-SH, Fv, scFv, F(ab′) 2 , and a diabody.

17. The binding compound of claim 6 , wherein the binding compound is an antibody fragment selected from the group consisting of Fab, Fab′, Fab′-SH, Fv, scFv, F(ab′) 2 , and a diabody.

18. The binding compound of claim 7 , wherein the binding compound is an antibody fragment selected from the group consisting of Fab, Fab′, Fab′-SH, Fv, scFv, F(ab′) 2 , and a diabody.

19. A pharmaceutical composition comprising the binding compound of claim 2 in combination with a pharmaceutically acceptable carrier or diluent.

20. A pharmaceutical composition comprising the binding compound of claim 3 in combination with a pharmaceutically acceptable carrier or diluent.

21. A pharmaceutical composition comprising the binding compound of claim 4 in combination with a pharmaceutically acceptable carrier or diluent.

22. A pharmaceutical composition comprising the binding compound of claim 5 in combination with a pharmaceutically acceptable carrier or diluent.

23. A pharmaceutical composition comprising the binding compound of claim 6 in combination with a pharmaceutically acceptable carrier or diluent.

24. A pharmaceutical composition comprising the binding compound of claim 7 in combination with a pharmaceutically acceptable carrier or diluent.

25. A pharmaceutical composition comprising the binding compound of claim 8 in combination with a pharmaceutically acceptable carrier or diluent.

26. A pharmaceutical composition comprising the binding compound of claim 9 in combination with a pharmaceutically acceptable carrier or diluent.

27. A pharmaceutical composition comprising the binding compound of claim 10 in combination with a pharmaceutically acceptable carrier or diluent.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 10, 2018
From: PRESTA, LEONARD G.; BEYER, BRIAN M.; ORTH, PETER; LIU, YAN-HUI; INGRAM, RICHARD N.
To: SCHERING CORPORATION
Reel/Frame 045774/0903 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 10, 2018
From: PRESTA, LEONARD G.; BEYER, BRIAN M.; INGRAM, RICHARD N.; ORTH, PETER; LIU, YAN-HUI
To: SCHERING CORPORATION
Reel/Frame 045774/0913 →
CHANGE OF NAME Recorded Aug 30, 2012
From: SCHERING CORPORATION
To: MERCK SHARP & DOHME CORP.
Reel/Frame 028884/0151 →