Antibodies binding AXL
View Patent ↗The present invention relates to anti-AXL antibodies, immunoconjugates, compositions and method of treatment of cancer with such anti-AXL antibodies, immunoconjugates, or compositions.
1. An antibody which binds to AXL (SEQ ID NO: 130) and comprises a heavy chain variable (VH) region and a light chain variable (VL) region, wherein the VH region comprises the CDR1, CDR2, and CDR3 sequences set forth in SEQ ID NOs: 36, 37, and 38, respectively, and the VL region comprises the CDR1, CDR2, and CDR3 sequences set forth in SEQ ID NO: 39, GAS, and SEQ ID NO: 40, respectively.
2. The antibody of claim 1 , wherein the VH and VL regions comprise the amino acid sequences set forth in SEQ ID NOs: 1 and 2, respectively.
3. The antibody of claim 1 , wherein said antibody comprises a heavy chain of an isotype selected from the group consisting of IgG1, IgG2, IgG3, and IgG4.
4. The antibody of claim 1 , which is a full-length monoclonal antibody.
5. The antibody of claim 1 , wherein said antibody is a monovalent antibody.
6. The antibody of claim 1 , wherein said antibody is a single-chain antibody.
7. An immunoconjugate comprising the antibody of claim 1 , and a therapeutic moiety.
8. The immunoconjugate of claim 7 , wherein the therapeutic moiety is a cytotoxic agent.
9. The immunoconjugate of claim 8 , wherein said cytotoxic agent is linked to said antibody with a cleavable linker.
10. The immunoconjugate of claim 9 , wherein said linker is mc-vc-PAB and the cytotoxic agent is MMAE; or the linker is SSP and the cytotoxic agent is DM1.
11. A pharmaceutical composition comprising the immunoconjugate of claim 7 , and a pharmaceutical acceptable carrier.
12. A pharmaceutical composition comprising the antibody of claim 1 , and a pharmaceutical acceptable carrier.
13. A kit for detecting the presence of AXL antigen, or a cell expressing AXL, in a sample, wherein the kit comprises the antibody of claim 1 .
14. A bispecific antibody comprising (a) a first binding region which binds to AXL (SEQ ID NO: 130) and comprises a heavy chain variable (VH) region and a light chain variable (VL) region, wherein the VH region comprises the CDR1, CDR2, and CDR3 sequences set forth in SEQ ID NOs: 36, 37, and 38, respectively, and the VL region comprises the CDR1, CDR2, and CDR3 sequences set forth in SEQ ID NO: 39, GAS, and SEQ ID NO: 40, respectively, and (b) a second binding region which binds a different target or epitope than said first binding region.
15. The bispecific antibody of claim 14 , wherein said bispecific antibody comprises a first and a second heavy chain, each of said first and second heavy chain comprises at least a hinge region, a CH2 and CH3 region, wherein in said first heavy chain at least one of the amino acids in the positions corresponding to positions selected from the group consisting of K409, T366, L368, K370, D399, F405, and Y407 in a human IgG1 heavy chain has been substituted, and in said second heavy chain at least one of the amino acids in the positions corresponding to a position selected from the group consisting of F405, T366, L368, K370, D399, Y407, and K409 in a human IgG1 heavy chain has been substituted, wherein said substitutions of said first and said second heavy chains are not in the same positions, and wherein the numbering is according to the EU Index as set forth in Kabat.
16. The bispecific antibody of claim 14 , wherein the amino acid in the position corresponding to K409 in a human IgG1 heavy chain is R in said first heavy chain, and the amino acid in the position corresponding to F405 in a human IgG1 heavy chain is L in said second heavy chain, or vice versa, wherein the numbering is according to the EU Index as set forth in Kabat.
17. An immunoconjugate comprising the bispecific antibody of claim 14 , and a therapeutic moiety.
18. A pharmaceutical composition comprising the bispecific antibody of claim 14 , and a pharmaceutical acceptable carrier.
19. An antibody which binds to AXL (SEQ ID NO: 130) and comprises a heavy chain variable (VH) region and a light chain variable (VL) region, wherein the VH region comprises the amino acid sequence set forth in SEQ ID NO: 1, and the VL region comprises the amino acid sequence set forth in SEQ ID NO: 2.
20. The antibody of claim 19 , wherein said antibody comprises a heavy chain of an isotype selected from the group consisting of IgG1, IgG2, IgG3, and IgG4.
21. The antibody of claim 19 , which is a full-length monoclonal antibody.
22. The antibody of claim 19 , wherein said antibody is a monovalent antibody.
23. The antibody of claim 19 , wherein said antibody is a single-chain antibody.
24. An immunoconjugate comprising the antibody of claim 19 , and a therapeutic moiety.
25. The immunoconjugate of claim 24 , wherein the therapeutic moiety is a cytotoxic agent.
26. A pharmaceutical composition comprising the antibody of claim 19 , and a pharmaceutical acceptable carrier.
27. A kit for detecting the presence of AXL antigen, or a cell expressing AXL, in a sample wherein the kit comprises the antibody of claim 19 .
28. A bispecific antibody comprising (a) a first binding region which binds to AXL (SEQ ID NO: 130) and comprises a heavy chain variable (VH) region and a light chain variable (VL) region, wherein the VH region comprises the amino acid sequence set forth in SEQ ID NO: 1, and the VL region comprises the amino acid sequence set forth in SEQ ID NO: 2, and (b) a second binding region which binds a different target or epitope than said first binding region.