Molecules that are able to inhibit the binding between NGF and the TrkA receptor as analgesics with prolonged effect
View Patent ↗Use of an anti-NGF antibody capable of inhibiting the binding between NGF and TrkA, capable of blocking the biological activity of TrkA for the preparation of a medicament for treating and/or preventing chronic pain.
1. A method of treatment of chronic pain in a subject comprising administering to the subject an effective amount of an anti-NGF antibody capable of inhibiting binding NGF and TrkA to treat chronic pain in said subject, wherein (a) the variable region of the antibody light chain comprises three complementarity determining regions (CDRs) having the sequences of from amino acid 24 to amino acid 34 of SEQ ID NO. 1; from amino acid 50 to amino acid 56 of SEQ ID NO. 1; and from amino acid 89 to amino acid 97 of SEQ ID NO. 1; and (b) the variable region of the antibody heavy chain comprises three of the complementarity determining regions (CDRs) having the sequences of amino acid 26 to amino acid 35 of SEQ ID NO. 2; from amino acid 50 to amino acid 65 of SEQ ID NO. 2; and from amino acid 98 to amino acid 111 of SEQ ID NO. 2.
2. The method of claim 1 wherein the antibody blocks the biological activity of TrkA.
3. The method of claim 1 wherein the variable region of the antibody light chain comprises the sequence of SEQ ID No. 1.
4. The method of claim 1 wherein the variable region of the antibody heavy chain comprises the sequence of SEQ ID No. 2.
5. The method of claim 1 wherein the antibody is in single chain form and comprises a light chain variable region and a heavy chain variable region joined by a linker.
6. The method of claim 1 wherein the antibody comprises two light chains and two heavy chains.
7. The method of claim 1 wherein the anti-NGF antibody is a humanized antibody.
8. The method of claim 7 wherein the variable region of the humanized antibody light chain comprises the sequence of SEQ ID No. 3.
9. The method of claim 7 wherein the variable region of the humanized antibody heavy chain comprises the sequence of SEQ ID No. 4.
10. The method of claim 7 wherein the humanized antibody light chain has the sequence of SEQ ID NO. 8.
11. The method of claim 7 wherein the humanized antibody heavy chain has a sequence selected from SEQ ID No. 5, SEQ ID No. 6, SEQ ID No. 7.
12. The method of claim 1 wherein the chronic pain is of the chronic inflammatory type.
13. The method of claim 12 wherein the chronic pain is caused by pancreatitis, kidney stones, headaches, dysmenorrhea, musculoskeletal pain, sprains, visceral pain, ovarian cysts, prostatitis, cystitis, interstitial cystitis, post-operative pain, migraine, trigeminal neuralgia, pain from burns and/or wounds, pain associated with trauma, neuropathic pain, pain associated with musculoskeletal diseases, rheumatoid arthritis, osteoarthritis, ankylosing spondylitis, periarticular pathologies, oncological pain, pain from bone metastases, pain from HIV.
14. The method of claim 1 wherein the pain is neuropathic pain.
15. The method of claim 1 wherein the pain is oncological pain.
16. The method of claim 1 wherein the antibody has a long duration of action.
17. The method of claim 1 , wherein said antibody is administered at a frequency of not more than once per week.
18. The method of claim 1 , wherein said antibody is a rat IgG1 isotype antibody.
19. The method of claim 1 , wherein said antibody is an IgG4 isotype antibody.
20. The method of claim 1 , wherein the variable region of the humanized antibody light chain comprises the sequence of SEQ ID NO: 3, the variable region of the humanized antibody heavy chain comprises the sequence of SEQ ID NO: 4, and the antibody is an IgG4 isotype antibody.