Fully human antibodies directed against the human insulin-like growth factor-1 receptor
This invention relates to human antibodies that bind to human insulin-like growth factor-1 receptor (IGF-IR), to derivatives of these antibodies (Fabs, single chain antibodies, bi-specific antibodes, or fusion proteins), and to uses of the antibodies and derivatives in therapeutic, and diagnostic methods. The invention relates to nucleic acids encoding the anti-IGF-IR, methods of generating the antibodies and expression. The invention further relates to combination therapies using ant-IGF-IR antibodies with anti-neoplastic drugs.
1. An isolated human antibody or fragment thereof, which specifically binds to insulin-like growth factor-I receptor (IGF-IR) comprising complementarity-determining regions (CDRs) having the amino acid sequence SEQ ID NO:14 at V H CDR1, SEQ ID NO:16 at V H CDR2, SEQ ID NO:18 at V H CDR3, SEQ ID NO:20 or 26 at V L CDR1, SEQ ID NO:22 or 28 at V L CDR2, and SEQ ID NO:24 or 30 at V L CDR3.
2. The antibody or fragment thereof of claim 1 , which comprises SEQ ID NO:14 at V H CDR1, SEQ ID NO:16 at V H CDR2, SEQ ID NO:18 at V H CDR3, SEQ ID NO:20 at V L CDR1, SEQ ID NO:22 at V L CDR2 and SEQ ID NO:24 at V L CDR3.
3. The antibody or fragment thereof of claim 1 , which comprises SEQ ID NO:14 at V H CDR1, SEQ ID NO:16 at V H CDR2, SEQ ID NO:18 at V H CDR3, SEQ ID NO:26 at V L CDR1, SEQ ID NO:28 at V L CDR2 and SEQ ID NO:30 at V L CDR3.
4. A pharmaceutical composition comprising the antibody or fragment thereof of claim 1 and a pharmaceutically acceptable carrier.
5. A conjugate comprising the antibody or fragment thereof of claim 1 linked to a cytotoxic agent.
6. A conjugate comprising the antibody or fragment thereof of claim 1 linked to a label.
7. A therapeutic composition effective to inhibit growth of human tumor cells that express IGF-IR, which composition comprises the antibody or fragment thereof of claim 1 .
8. The therapeutic composition of claim 7 , which further comprises an antineoplastic agent.
9. The therapeutic composition of claim 8 , wherein the anti-neoplastic agent is an inhibitor of topoisomerase I or topoisomerase II.
10. The therapeutic composition of claim 8 , wherein the anti-neoplastic agent is selected from the group consisting of irinotecan, camptothecan, and etoposide.
11. A therapeutic composition effective to promote regression of human tumors that express IGF-IR, which composition comprises the antibody or fragment thereof of claim 1 .
12. The therapeutic composition of claim 11 , which further comprises an antineoplastic agent.
13. The therapeutic composition of claim 12 , wherein the anti-neoplastic agent is an inhibitor of topoisomerase I or topoisomerase II.
14. The therapeutic composition of claim 12 , wherein the anti-neoplastic agent is selected from the group consisting of irinotecan, camptothecan, and etoposide.
15. An isolated human antibody or fragment thereof comprising the heavy chain variable domain of SEQ ID NO:2 and the light chain variable domain of SEQ ID NO:6.
16. An isolated human antibody or fragment thereof comprising the heavy chain variable domain of SEQ ID NO:2 and the light chain variable domain of SEQ ID NO:10.
17. The antibody of claims 15 or 16 , wherein said antibody has an IgG1 isotype.
18. A pharmaceutical composition comprising the antibody of claim 15 or 16 and a pharmaceutically acceptable carrier.
19. A method of neutralizing the activation of IGF-IR, which comprises administering to a mammal an effective amount of the antibody or fragment thereof of claim 1 .
20. A method of reducing tumor growth which comprises administering to a mammal an effective amount of the antibody or fragment thereof of claim 1 .
21. The method of claim 20 , which further comprises administering an effective amount of an anti-neoplastic agent.
22. The method of claim 21 , wherein the anti-neoplastic agent is an inhibitor of topoisomerase I or topoisomerase II.
23. The method of claim 21 , wherein the anti-neoplastic agent is selected from the group consisting of irinotecan, camptothecan, and etoposide.
24. A method of promoting tumor regression which comprises administering to a mammal an effective amount of the antibody or fragment thereof of claim 1 .
25. The method of claim 24 , which further comprises administering an effective amount of an anti-neoplastic agent.
26. The method of claim 25 , wherein the anti-neoplastic agent is an inhibitor of topoisomerase I or topoisomerase II.
27. The method of claim 25 , wherein the anti-neoplastic agent is selected from the group consisting of irinotecan, camptothecan, and etoposide.
28. The method of any one of claims 20 to 27 , wherein the tumor is a breast tumor, colorectal tumor, pancreatic tumor, ovarian tumor, lung tumor, prostate tumor, bone or soft tissue sarcoma or myeloma.