IP Library Granted Patent US 8,575,317
Granted Patent B2
US 8,575,317 · App. 12/809,138 · Granted Nov 5, 2013

Anti-NR10 antibody and use thereof

Inventors: Taichi Kuramochi (Shizuoka, JP); Keiko Kasutani (Shizuoka, JP); Souhei Ohyama (Shizuoka, JP); Hiroyuki Tsunoda (Shizuoka, JP); Tomoyuki Igawa (Shizuoka, JP); Tatsuhiko Tachibana (Shizuoka, JP); Hirotake Shiraiwa (Shizuoka, JP); Keiko Esaki (Shizuoka, JP)
Assignee: Chugai Seiyaku Kabushiki Kaisha
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Quick Facts
Patent No.
US 8,575,317
App. No.
12/809,138
Granted
Nov 5, 2013
Kind
B2
Abstract

The present inventors successfully obtained anti-NR10 antibodies having an effective neutralizing activity against NR10. The anti-NR10 antibodies provided by the present invention are useful as, for example, pharmaceuticals for treating or preventing inflammatory diseases.

Claims (38)

1. An isolated anti-NR10 antibody selected from the group consisting of:

(1) an antibody comprising a heavy chain variable region comprising the amino acid sequence of SEQ ID NO: 206 and a light chain variable region comprising the amino acid sequence of SEQ ID NO: 220;

(2) an antibody comprising a heavy chain variable region comprising the amino acid sequence of SEQ ID NO: 207 and a light chain variable region comprising the amino acid sequence of SEQ ID NO: 220;

(3) an antibody comprising a heavy chain variable region comprising the amino acid sequence of SEQ ID NO: 208 and a light chain variable region comprising the amino acid sequence of SEQ ID NO: 220;

(4) an antibody comprising a heavy chain variable region comprising the amino acid sequence of SEQ ID NO: 209 and a light chain variable region comprising the amino acid sequence of SEQ ID NO: 220;

(5) an antibody comprising a heavy chain variable region comprising the amino acid sequence of SEQ ID NO: 210 and a light chain variable region comprising the amino acid sequence of SEQ ID NO: 220;

(6) an antibody comprising a heavy chain variable region comprising the amino acid sequence of SEQ ID NO: 211 and a light chain variable region comprising the amino acid sequence of SEQ ID NO: 220;

(7) an antibody comprising a heavy chain variable region comprising the amino acid sequence of SEQ ID NO: 212 and a light chain variable region comprising the amino acid sequence of SEQ ID NO: 220;

(8) an antibody comprising a heavy chain variable region comprising the amino acid sequence of SEQ ID NO: 213 and a light chain variable region comprising the amino acid sequence of SEQ ID NO: 220;

(9) an antibody comprising a heavy chain variable region comprising the amino acid sequence of SEQ ID NO: 214 and a light chain variable region comprising the amino acid sequence of SEQ ID NO: 220;

(10) an antibody comprising a heavy chain variable region comprising the amino acid sequence of SEQ ID NO: 215 and a light chain variable region comprising the amino acid sequence of SEQ ID NO: 220;

(11) an antibody comprising a heavy chain variable region comprising the amino acid sequence of SEQ ID NO: 216 and a light chain variable region comprising the amino acid sequence of SEQ ID NO: 221; and

(12) an antibody comprising a heavy chain variable region comprising the amino acid sequence of SEQ ID NO: 217 and a light chain variable region comprising the amino acid sequence of SEQ ID NO: 221.

2. A pharmaceutical composition comprising the antibody of claim 1 .

3. An isolated anti-NR10 antibody selected from the group consisting of:

(1) an antibody comprising a heavy chain comprising the amino acid sequence of SEQ ID NO: 224 and a light chain comprising the amino acid sequence of SEQ ID NO: 238;

(2) an antibody comprising a heavy chain comprising the amino acid sequence of SEQ ID NO: 225 and a light chain comprising the amino acid sequence of SEQ ID NO: 238;

(3) an antibody comprising a heavy chain comprising the amino acid sequence of SEQ ID NO: 226 and a light chain comprising the amino acid sequence of SEQ ID NO: 238;

(4) an antibody comprising a heavy chain comprising the amino acid sequence of SEQ ID NO: 227 and a light chain comprising the amino acid sequence of SEQ ID NO: 238;

(5) an antibody comprising a heavy chain comprising the amino acid sequence of SEQ ID NO: 228 and a light chain comprising the amino acid sequence of SEQ ID NO: 238;

(6) an antibody comprising a heavy chain comprising the amino acid sequence of SEQ ID NO: 229 and a light chain comprising the amino acid sequence of SEQ ID NO: 238;

(7) an antibody comprising a heavy chain comprising the amino acid sequence of SEQ ID NO: 230 and a light chain comprising the amino acid sequence of SEQ ID NO: 238;

(8) an antibody comprising a heavy chain comprising the amino acid sequence of SEQ ID NO: 231 and a light chain comprising the amino acid sequence of SEQ ID NO: 238;

(9) an antibody comprising a heavy chain comprising the amino acid sequence of SEQ ID NO: 232 and a light chain comprising the amino acid sequence of SEQ ID NO: 238;

(10) an antibody comprising a heavy chain comprising the amino acid sequence of SEQ ID NO: 233 and a light chain comprising the amino acid sequence of SEQ ID NO: 238;

(11) an antibody comprising a heavy chain comprising the amino acid sequence of SEQ ID NO: 234 and a light chain comprising the amino acid sequence of SEQ ID NO: 239; and

(12) an antibody comprising a heavy chain comprising the amino acid sequence of SEQ ID NO: 235 and a light chain comprising the amino acid sequence of SEQ ID NO: 239.

4. A pharmaceutical composition comprising the antibody of claim 3 .

5. A method of treating atopic dermatitis in a subject in need thereof, the method comprising administering to the subject a therapeutically effective amount of the pharmaceutical composition of claim 2 .

6. A method of treating atopic dermatitis in a subject in need thereof, the method comprising administering to the subject a therapeutically effective amount of the pharmaceutical composition of claim 4 .

7. A method of treating chronic dermatitis in a subject in need thereof, the method comprising administering to the subject a therapeutically effective amount of the pharmaceutical composition of claim 2 .

8. A method of treating chronic dermatitis in a subject in need thereof, the method comprising administering to the subject a therapeutically effective amount of the pharmaceutical composition of claim 4 .

9. A method of treating rheumatism in a subject in need thereof, the method comprising administering to the subject a therapeutically effective amount of the pharmaceutical composition of claim 2 .

10. A method of treating rheumatism in a subject in need thereof, the method comprising administering to the subject a therapeutically effective amount of the pharmaceutical composition of claim 4 .

11. A method of treating osteoarthritis in a subject in need thereof, the method comprising administering to the subject a therapeutically effective amount of the pharmaceutical composition of claim 2 .

12. A method of treating osteoarthritis in a subject in need thereof, the method comprising administering to the subject a therapeutically effective amount of the pharmaceutical composition of claim 4 .

13. A method of treating rheumatoid arthritis in a subject in need thereof, the method comprising administering to the subject a therapeutically effective amount of the pharmaceutical composition of claim 2 .

14. A method of treating rheumatoid arthritis in a subject in need thereof, the method comprising administering to the subject a therapeutically effective amount of the pharmaceutical composition of claim 4 .

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 23, 2010
From: KURAMOCHI, TAICHI; KASUTANI, KEIKO; OHYAMA, SOUHEI; TSUNODA, HIROYUKI; IGAWA, TOMOYUKI; TACHIBANA, TATSUHIKO; SHIRAIWA, HIROTAKE; ESAKI, KEIKO
To: CHUGAI SEIYAKU KABUSHIKI KAISHA
Reel/Frame 025064/0078 →
Priority Claims (2)
WO PCT/JP2008/072152 · Dec 5, 2008 · international
WO PCT/JP2009/054941 · Mar 13, 2009 · international
Continuity (1)
Related Publication 20110229459A1 · Sep 22, 2011