IP Library › Granted Patent US 10,259,867
Granted Patent B2
US 10,259,867 · App. 15/583,487 · Granted Apr 16, 2019

Method for treating lupus by administering an anti-IL-12 antibody

Inventors: Jill Giles-Komar (Downingtown, PA); David M. Knight (Berwyn, PA); David Peritt (Lake Forest, IL); Bernard Scallon (Wayne, PA); David Shealy (Downingtown, PA)
Assignee: Janssen Biotech, Inc.
C07K16/244A61K39/3955A61K45/06A61K2039/505C07K2317/21C07K2317/565C07K2317/76C07K2317/92
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Quick Facts
Patent No.
US 10,259,867
App. No.
15/583,487
Granted
Apr 16, 2019
Kind
B2
Abstract

Isolated anti-IL-12 antibodies, nucleic acids encoding antibodies or antibody portions, vectors, host cells, and methods of making are useful for production of antibody or portions for treating and/or diagnosing IL-12 related conditions, diseases, and disorders, such as psoriasis.

Claims (16)

1. A method for reducing symptoms of systemic lupus erythematosus in an animal, comprising administering a composition comprising an effective amount of an isolated anti-IL-12 antibody comprising a heavy chain variable region of the amino acid sequence of SEQ ID NO: 7 and a light chain variable region of the amino acid sequence of SEQ ID NO: 8, to said animal.

2. The method according to claim 1 , wherein said effective amount is 0.001-50 mg/kilogram of said animal.

3. The method according to claim 1 , wherein said administering is subcutaneous.

4. The method according to claim 1 , further comprising administering at least one composition comprising an effective amount of a cytokine antagonist.

5. A method for reducing symptoms of systemic lupus erythematosus in an animal, comprising administering a composition comprising an effective amount of an isolated anti-IL-12 antibody comprising a heavy chain complementarity determining region CDR 1 of the amino acid sequence of SEQ ID NO: 1, a heavy chain CDR2 of the amino acid sequence of SEQ ID NO: 2, a heavy chain CDR3 of the amino acid sequence of SEQ ID NO: 3, a light chain CDR1 of the amino acid sequence of SEQ ID NO: 4, a light chain CDR2 of the amino acid sequence of SEQ ID NO: 5, and a light chain CDR3 of the amino acid sequence of SEQ ID NO: 6, to said animal.

6. The method according to claim 5 , wherein said effective amount is 0.001-50 mg/kilogram of said animal.

7. The method according to claim 5 , wherein said administering is subcutaneous.

8. The method according to claim 5 , further comprising administering at least one composition comprising an effective amount of a cytokine antagonist.

9. A method for reducing symptoms of systemic lupus erythematosus in a human, comprising administering a composition comprising an effective amount of an isolated anti-IL-12 antibody comprising a heavy chain variable region of the amino acid sequence of SEQ ID NO: 7 and a light chain variable region of the amino acid sequence of SEQ ID NO: 8, to said human.

10. The method according to claim 9 , wherein said effective amount is 0.001-50 mg/kilogram of said human.

11. The method according to claim 9 , wherein said administering is subcutaneous.

12. The method according to claim 9 , further comprising administering at least one composition comprising an effective amount of a cytokine antagonist.

13. A method for reducing symptoms of systemic lupus erythematosus in a human, comprising administering a composition comprising an effective amount of an isolated anti-IL-12 antibody comprising a heavy chain complementarity determining region CDR 1 of the amino acid sequence of SEQ ID NO: 1, a heavy chain CDR2 of the amino acid sequence of SEQ ID NO: 2, a heavy chain CDR3 of the amino acid sequence of SEQ ID NO: 3, a light chain CDR1 of the amino acid sequence of SEQ ID NO: 4, a light chain CDR2 of the amino acid sequence of SEQ ID NO: 5, and a light chain CDR3 of the amino acid sequence of SEQ ID NO: 6, to said human.

14. The method according to claim 13 , wherein said effective amount is 0.001-50 mg/kilogram of said human.

15. The method according to claim 13 , wherein said administering is subcutaneous.

16. The method according to claim 13 , further comprising administering at least one composition comprising an effective amount of a cytokine antagonist.

Continuity (12)
Division 15198678 · Jun 30, 2016
Division 14190893 · Feb 26, 2014
Division 13670918 · Nov 7, 2012
Division 13299874 · Nov 18, 2011
Division 12971626 · Dec 17, 2010
Division 12500120 · Jul 9, 2009
Division 11668256 · Jan 29, 2007
Division 10975883 · Oct 28, 2004
Division 09920262 · Aug 1, 2001
Provisional Application 60223358 · Aug 7, 2000
Provisional Application 60236827 · Sep 29, 2000
Related Publication 20180334500A1 · Nov 22, 2018
Cited By (2)
US 12,247,071 US 12,258,393