IP Library Granted Patent US 7,807,155
Granted Patent B2
US 7,807,155 · App. 11/658,344 · Granted Oct 5, 2010

IL-17 antagonistic antibodies

Assignee: Novartis AG
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 7,807,155
App. No.
11/658,344
Granted
Oct 5, 2010
Kind
B2
Abstract

An IL-17 binding molecule, in particular an antibody to human IL-17, more preferably a human antibody to human IL-17 is provided, wherein the hypervariable regions of the heavy and light chains have amino acid sequences as defined, for use in the treatment of an IL-17 mediated disease or disorder, e.g. rheumatoid arthritis.

Claims (22)

1. A purified IL-17 binding molecule comprising a heavy chain variable domain comprising SEQ ID NO:8.

2. A purified IL-17 binding molecule comprising a light chain variable domain comprising SEQ ID NO:10.

3. A purified IL-17 binding molecule comprising a heavy chain variable domain comprising SEQ ID NO:8 and a light chain variable domain comprising SEQ ID NO:10.

4. A purified IL-17 binding molecule comprising a heavy chain variable domain comprising the three Complementarity-Determining Regions (CDRs) of SEQ ID NO:8 and a light chain variable domain comprising the three CDRs of SEQ ID NO:10.

5. The purified IL-17 binding molecule of claim 4 , wherein said three CDRs of SEQ ID NO:8 are set forth in SEQ ID NO:1, SEQ ID NO:2 and SEQ ID NO:3.

6. The purified IL-17 binding molecule of claim 4 , wherein said three CDRs of SEQ ID NO:8 are set forth in SEQ ID NO:11, SEQ ID NO:12 and SEQ ID NO:13.

7. The purified IL-17 binding molecule of claim 5 , wherein said three CDRs of SEQ ID NO:10 are set forth in SEQ ID NO:4, SEQ ID NO:5 and SEQ ID NO:6.

8. The purified IL-17 binding molecule of claim 6 , wherein said three CDRs of SEQ ID NO:10 are set forth in SEQ ID NO:4, SEQ ID NO:5 and SEQ ID NO:6.

9. The purified IL-17 binding molecule of either claim 7 or 8 , wherein said IL-17 binding molecule is a human antibody.

10. A pharmaceutical composition comprising the purified IL-17 binding molecule of either claim 7 or 8 and a pharmaceutically acceptable diluent, excipient, carrier or mixture thereof.

11. A pharmaceutical composition comprising the purified IL-17 binding molecule of claim 9 and a pharmaceutically acceptable diluent, excipient, carrier or mixture thereof.

12. A method for inhibiting the binding of IL-17 to an IL-17 receptor in a subject, comprising administering to the subject the purified IL-17 binding molecule of either claim 7 or 8 in an amount effective to inhibit the binding of IL-17 to the IL-17 receptor in the subject.

13. A method for inhibiting the binding of IL-17 to an IL-17 receptor in a subject, comprising administering to the subject the purified IL-17 binding molecule of claim 9 in an amount effective to inhibit the binding of IL-17 to the IL-17 receptor in the subject.

14. A method for inhibiting the binding of IL-17 to an IL-17 receptor in a subject, comprising administering to the subject the pharmaceutical composition of claim 11 in an amount effective to inhibit the binding of IL-17 to the IL-17 receptor in the subject.

15. A method for binding IL-17 in a subject, comprising administering to the subject the purified IL-17 binding molecule of either claim 7 or 8 in an amount effective to bind IL-17 in the subject.

16. A method for binding IL-17 in a subject, comprising administering to the subject the purified IL-17 binding molecule of claim 9 in an amount effective to bind IL-17 in the subject.

17. A method for binding IL-17 in a subject, comprising administering to the subject the pharmaceutical composition of claim 11 in an amount effective to bind IL-17 in the subject.

18. A method for treating an IL-17 mediated inflammatory condition or IL-17 mediated autoimmune disease in a subject, comprising administering to the subject in need thereof an effective amount of the purified IL-17 binding molecule of either claim 7 or 8 .

19. A method for treating an IL-17 mediated inflammatory condition or IL-17 mediated autoimmune disease in a subject, comprising administering to the subject in need thereof an effective amount of the purified IL-17 binding molecule of claim 9 .

20. A method for treating an IL-17 mediated inflammatory condition or IL-17 mediated autoimmune disease in a subject, comprising administering to the subject in need thereof an effective amount of the pharmaceutical composition of claim 11 .

21. The method according to claim 19 , wherein said IL-17 mediated inflammatory condition or autoimmune disease is rheumatoid arthritis.

22. The method according to claim 19 , wherein said IL-17 mediated inflammatory condition or autoimmune disease is psoriasis.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 11, 2026
From: NOVARTIS AG
To: NOVARTIS PHARMA AG
Reel/Frame 075712/0291 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 9, 2010
From: DI PADOVA, FRANCO E; GRAMM, HERMANN; HOFSTETTER, HANS; JESCHKE, MARGIT; RONDEAU, JEAN-MICHEL; VAN DEN BERG, WIM
To: NOVARTIS AG
Reel/Frame 023916/0165 →
Priority Claims (1)
GB 0417487.6 · Aug 5, 2004 · national
Continuity (1)
Related Publication 20090280131A1 · Nov 12, 2009