METHODS OF TREATING INFLAMMATORY PAIN

1 . A method of reducing incidence of or treating inflammatory pain or symptoms of inflammatory pain, comprising peripheral administration to the individual of an effective amount of an anti-CGRP antagonist antibody.

2 . The method according to claim 1 , wherein the medicament is prepared to be peripherally administered.

3 . The method according to claim 1 , wherein the medicament is administered peripherally.

4 . The method according to claim 1 , wherein the medicament is prepared to be administered orally, sublingually, via inhalation, transdermally, subcutaneously, intravenously, intra-arterially, intra-articularly, peri-articularly, locally or intramuscularly.

5 . The method according to claim 4 , wherein the medicament is prepared to be administered subcutaneously or intravenously.

6 . The method according to claim 1 , wherein the anti-CGRP antagonist antibody acts peripherally on administration.

7 . (canceled)

8 . (canceled)

9 . The method according to claim 1 , wherein the anti-CGRP antagonist antibody has one or more of the following characteristics:

(a) binds to CGRP;

(b) blocks CGRP from binding to its receptor;

(c) blocks or decreases CGRP receptor activation;

(d) inhibits blocks, suppresses or reduces CGRP biological activity;

(e) increases clearance of CGRP; or

(g) inhibits CGRP synthesis, production or release.

10 . The method according to claim 1 , wherein the anti-CGRP antagonist antibody has one or more of the following characteristics:

(i) is a human antibody,

(ii) is a humanized antibody,

(iii) is a monoclonal antibody,

(iv) binds CGRP with a Kd of 50 nM or less (as measured by surface plasmon resonance at 37° C.); or

(v) has a half life in-vivo of at least 7 days.

11 . The method according to claim 1 , wherein the anti-CGRP antagonist antibody specifically binds to the C-terminal region of CGRP.

12 . The method according to claim 10 , wherein the anti-CGRP antagonist antibody specifically recognises the epitope defined by the sequence GSKAF.

13 - 15 . (canceled)

16 . The method according to claim 1 , wherein the anti-CGRP antibody comprises at least one CDR selected from the group consisting of:

(a) CDR H1 as set forth in SEQ ID NO: 3 or 21;

(b) CDR H2 as set forth in SEQ ID NO: 4 or 22;

(c) CDR H3 as set forth in SEQ ID NO: 5 or 23;

(d) CDR L1 as set forth in SEQ ID NO: 6 or 24;

(e) CDR L2 as set forth in SEQ ID NO: 7 or 25;

(f) CDR L3 as set forth in SEQ ID NO: 8 or 26; and

(g) variants of L1, L2 and H2.

17 . (canceled)

18 . The method according to claim 1 , wherein the anti-CGRP antibody comprises a heavy chain produced by the expression vector with ATCC Accession No. PTA-6867.

19 . The method according to claim 1 , wherein the anti-CGRP antibody comprises a light chain produced by the expression vector with ATCC Accession No. PTA-6866.

20 . The method according to claim 1 , wherein the anti-CGRP antibody is produced by the expression vectors with ATCC Accession Nos. PTA-6867 and PTA-6866.

21 . The method according to claim 1 , wherein the medicament is prepared for peripheral administration by sub-cutaneous or intra-venous injection between once, twice, three or four times per month.

22 . The method according to claim 1 , wherein the medicament is prepared for peripheral administration with an antibody concentration of between 5 to 100 mg/ml

23 . The method according to claim 1 , wherein the medicament is prepared for peripheral administration with an antibody concentration of between 1 to 100 mg/kg of body weight.

24 - 26 . (canceled)

27 . The method according to claim 1 , wherein the anti-CGRP antibody is administered separately, sequentially or simultaneously in combination with one or more further pharmacologically active compounds.

28 . (canceled)

29 . (canceled)

30 . A pharmaceutical composition for reducing incidence of or treating inflammatory pain or symptoms of inflammatory pain in an individual, comprising an anti-CGRP antagonist antibody and a pharmaceutically acceptable carrier wherein the composition is prepared to be peripherally administered.

31 . A kit comprising:

(a) a pharmaceutical composition according to claim 30 , and

(b) instructions for the peripheral administration of an therapeutically effective amount of said pharmaceutical composition to an individual for reducing incidence of or treating inflammatory pain or symptoms of inflammatory pain.