IP Library › Granted Patent US 7,910,708
Granted Patent B2
US 7,910,708 · App. 12/091,020 · Granted Mar 22, 2011

Anti-IL13 human antibodies

Assignee: Novartis AG
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Quick Facts
Patent No.
US 7,910,708
App. No.
12/091,020
Granted
Mar 22, 2011
Kind
B2
Abstract

The present invention relates to human anti-IL-13 binding molecules, particularly antibodies, and to methods for using anti-IL-13 antibody molecules in diagnosis or treatment of IL-13 related disorders, such as asthma, atopic dermatitis, allergic rhinitis, fibrosis, inflammatory bowel disease and Hodgkin's lymphoma.

Claims (17)

1. An isolated anti-IL-13 antibody, or antigen-binding fragment thereof, comprising H-CDR1, H-CDR2 and H-CDR3 selected from (i)-(ii):

(i) SEQ ID NO: 6, SEQ ID NO:8, and SEQ ID NO: 9, respectively; and

(ii) SEQ ID NO: 7, SEQ ID NO:8, and SEQ ID NO: 10, respectively;

and comprising L-CDR1, L-CDR2 and L-CDR3 selected from (iii)-(v):

(iii) SEQ ID NO: 16. SEQ ID NO: 19, and SEQ ID NO: 20, respectively;

(iv) SEQ ID NO: 17, SEQ ID NO: 19, and SEQ ID NO: 21, respectively; and

(v) SEQ ID NO: 18. SEQ ID NO: 19, and SEQ ID NO: 22, respectively.

2. The antibody according to claim 1 which comprises a heavy chain variable region having an amino acid sequence selected from any one of SEQ ID NO: 23, 27, 31 and 35.

3. The antibody according to claim 1 which comprises a light chain variable region having the amino acid sequence selected from any one of SEQ ID NO: 25, 29, 33 and 37.

4. An isolated anti-IL-13 antibody, or antigen-binding fragment thereof, comprising a heavy chain variable region having an amino acid sequence selected from any one of SEQ ID NO: 23, 27, 31 and 35, and a light chain variable region having the amino acid sequence selected from any one of SEQ ID NO: 25, 29, 33 and 37.

5. The antibody according to claim 4 comprising a heavy chain variable region according to SEQ ID NO: 23 and a light chain variable region according to SEQ ID NO:25.

6. The antibody according to claim 4 comprising a heavy chain variable region according to SEQ ID NO: 27 and a light chain variable region according to SEQ ID NO: 29.

7. The antibody according to claim 4 comprising a heavy chain variable region according to SEQ ID NO: 31 and a light chain variable region according to SEQ ID NO: 33.

8. The antibody according to claim 4 comprising a heavy chain variable region according to SEQ ID NO: 35 and a light chain variable region according to SEQ ID NO: 37.

9. The antibody according to claim 1 which is an IgGI or an IgG4.

10. A pharmaceutical composition comprising an antibody or functional fragment thereof according to claim 1 and a pharmaceutically acceptable carrier or excipient therefore.

11. The antibody, or antigen-binding fragment, of claims 1 wherein the antibody is a human antibody, a humanized antibody, a Fab, or a scFV.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 31, 2011
From: CAMPBELL, EMMA MICHELLE; PARVEEN, SOFIA; BUECHLER, JOE; VALKIRS, GUNARS
To: NOVARTIS AG
Reel/Frame 025719/0417 →
Priority Claims (2)
GB 0521509.0 · Oct 21, 2005 · national
GB 0616666.4 · Aug 22, 2006 · national
Continuity (1)
Related Publication 20080267959A1 · Oct 30, 2008