Antagonist antibodies directed against calcitonin gene-related peptide and methods using same
The invention features methods for preventing or treating CGRP associated disorders such as vasomotor symptoms, including headaches (e.g., migraine, cluster headache, and tension headache) and hot flushes, by administering an anti-CGRP antagonist antibody. Antagonist antibody G1 and antibodies derived from G1 directed to CGRP are also described.
1. An isolated antibody comprising
a. CDR H1 as set forth in SEQ ID NO: 3:
b. CDR H2 as set forth in SEQ ID NO: 4, or variants as shown in Table 6;
c. CDR H3 as set forth in SEQ ID NO: 5:
d. CDR L1 as set forth in SEQ ID NO: 6, or variants as shown in Table 6;
e. CDR L2 as set forth in SEQ ID NO: 7, or variants as shown in Table 6; and
f. CDR L3 as set forth in SEQ ID NO: 8;
wherein the antibody has a binding affinity (K D ) to human α-CGRP of 50 nM or less as measured by surface plasmon resonance at 37° C.
2. The antibody according to claim 1 , comprising a V H domain that is at least 90% identical in amino acid sequence to SEQ ID NO: 1.
3. The antibody according to claim 2 , wherein the amino acid residue at position 99 of SEQ ID NO: 1 is L or is substituted by A, N, S, T, V or R, and wherein the amino acid residue at position 100 of SEQ ID NO: 1 is A, or is substituted by L, R, S, V, Y, C G, T, k, or P.
4. The antibody according to claim 1 , comprising a V L domain that is at least 90% identical in amino acid sequence to SEQ ID NO: 2.
5. An isolated antibody comprising a V H domain comprising SEQ ID NO: 1 and a V L domain comprising SEQ ID NO: 2.
6. The antibody of claim 5 , wherein the antibody is an IgG, an IgM, an IgE, an IgA, or an IgD molecule.
7. The antibody according to claim 5 , comprising a heavy chain produced by the expression vector with ATCC Accession No. PTA-6867.
8. The antibody according to claim 5 , comprising a light chain produced by the expression vector with ATCC Accession No. PTA-6866.
9. A pharmaceutical composition comprising the antibody according to claim 1 and a pharmaceutically acceptable excipient.