IP Library › Granted Patent US 9,783,607
Granted Patent B2
US 9,783,607 · App. 15/142,765 · Granted Oct 10, 2017

Human anti-IL-23 antibodies, compositions, methods and uses

Inventors: Jacqueline Benson (Malvern, PA); Jill Carton (Malvern, PA); Mark Cunningham (Kennett Square, PA); Yevgeniya I. Orlovsky (Chadds Ford, PA); Robert Rauchenberger (Martinsried, DE); Raymond Sweet (Bryn Mawr, PA)
Assignee: Janssen Biotech, Inc.
C07K16/244A61K9/0019A61K9/08A61K39/3955A61K47/183A61K47/26A61K2039/505C07K2317/21C07K2317/34C07K2317/52C07K2317/55C07K2317/565C07K2317/73C07K2317/76C07K2317/92C07K2319/00C07K2319/30
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Quick Facts
Patent No.
US 9,783,607
App. No.
15/142,765
Granted
Oct 10, 2017
Kind
B2
Abstract

A human anti-IL-23p19 antibody, including isolated nucleic acids that encode at least one anti-IL-23p19 antibody, vectors, host cells, and methods of making and using thereof have applications in diagnostic and/or therapeutic compositions, methods and devices.

Claims (26)

1. A prefilled syringe containing a liquid pharmaceutical formulation of an isolated IL-23p19 antibody, comprising a light chain variable region and a heavy chain variable region, said light chain variable region comprising:

a complementarity determining region light chain 1 (CDRL1) amino acid sequence of SEQ ID NO:50;

a CDRL2 amino acid sequence of SEQ ID NO:56; and

a CDRL3 amino acid sequence of SEQ ID NO:73,

said heavy chain variable region comprising:

a complementarity determining region heavy chain 1 (CDRH1) amino acid sequence of SEQ ID NO:5;

a CDRH2 amino acid sequence of SEQ ID NO:20; and

a CDRH3 amino acid sequence of SEQ ID NO:44.

2. The prefilled syringe of claim 1 , wherein the pH of the formulation is 5.8.

3. The prefilled syringe of claim 2 , wherein the liquid pharmaceutical formulation comprises histidine.

4. A prefilled syringe containing a liquid pharmaceutical formulation of an antibody comprising at least one member selected from the group consisting of a light chain variable region having the amino acid sequence of SEQ ID NO:116, a heavy chain variable region having the amino acid sequence of SEQ ID NO:106, and a heavy chain variable region having the amino acid sequence of SEQ ID NO:106 with up to three substitutions from residues 50-66 of the amino acid sequence of SEQ ID NO: 106.

5. The prefilled syringe of claim 4 , wherein the pH of the formulation is 5.8.

6. The prefilled syringe of claim 5 , wherein the liquid pharmaceutical formulation comprises histidine.

7. A prefilled syringe containing a liquid pharmaceutical formulation of an antibody comprising a light chain variable region having the amino acid sequence of SEQ ID NO:116 and a heavy chain variable region having the amino acid sequence of SEQ ID NO:106.

8. The prefilled syringe of claim 7 , wherein the pH of the formulation is 5.8.

9. The prefilled syringe of claim 7 , wherein the liquid pharmaceutical formulation comprises histidine.

10. A prefilled syringe containing a liquid pharmaceutical formulation of an antibody comprising a light chain variable region having the amino acid sequence of SEQ ID NO:116, a heavy chain variable region having the amino acid sequence of SEQ ID NO:106, wherein the liquid pharmaceutical formulation comprises histidine and the pH of the formulation is 5.8.

11. The prefilled syringe of claim 2 , wherein the liquid pharmaceutical formulation comprises sucrose.

12. The prefilled syringe of claim 2 , wherein the liquid pharmaceutical formulation comprises poly sorbate 80.

13. The prefilled syringe of claim 2 , wherein the liquid pharmaceutical formulation comprises water.

14. The prefilled syringe of claim 5 , wherein the liquid pharmaceutical formulation comprises sucrose.

15. The prefilled syringe of claim 5 , wherein the liquid pharmaceutical formulation comprises poly sorbate 80.

16. The prefilled syringe of claim 5 , wherein the liquid pharmaceutical formulation comprises water.

17. The prefilled syringe of claim 7 , wherein the liquid pharmaceutical formulation comprises sucrose.

18. The prefilled syringe of claim 7 , wherein the liquid pharmaceutical formulation comprises poly sorbate 80.

19. The prefilled syringe of claim 7 , wherein the liquid pharmaceutical formulation comprises water.

Continuity (6)
Division 13524122 · Jun 15, 2012
Division 13173090 · Jun 30, 2011
Division 12855354 · Aug 12, 2010
Division 11617503 · Dec 28, 2006
Provisional Application 60754889 · Dec 29, 2005
Related Publication 20160237151A1 · Aug 18, 2016