Antibody therapeutics that bind CD47
View Patent ↗There is disclosed compositions and methods relating to or derived from anti-CD47 antibodies. More specifically, there is disclosed fully human antibodies that bind CD47, CD47-antibody binding fragments and derivatives of such antibodies, and CD47-binding polypeptides comprising such fragments. Further still, there is disclosed nucleic acids encoding such antibodies, antibody fragments and derivatives and polypeptides, cells comprising such polynucleotides, methods of making such antibodies, antibody fragments and derivatives and polypeptides, and methods of using such antibodies, antibody fragments and derivatives and polypeptides, including methods of treating a disease.
1. A fully human anti-CD47 antibody, or an antigen-binding fragment thereof, comprising a heavy chain variable domain comprising complementarity determining regions (CDRs) as set forth in a heavy chain variable domain amino acid sequence selected from the group consisting of SEQ ID NO: 1, SEQ ID NO: 7, SEQ ID NO: 9, SEQ ID NO: 10, SEQ ID NO: 11, SEQ ID NO: 12, SEQ ID NO: 13, SEQ ID NO: 14, SEQ ID NO: 16, SEQ ID NO: 17, SEQ ID NO: 18, SEQ ID NO: 22, SEQ ID NO: 24, and SEQ ID NO: 32; and comprising a light chain variable domain comprising CDRs as set forth in a light chain variable region amino acid sequence selected from the group consisting of SEQ ID NO: 2, SEQ ID NO: 4, SEQ ID NO: 5, SEQ ID NO: 6, SEQ ID NO: 8, SEQ ID NO: 15, SEQ ID NO: 19, SEQ ID NO: 20, SEQ ID NO: 21, SEQ ID NO: 23, SEQ ID NO: 25, SEQ ID NO: 26, SEQ ID NO: 27, SEQ ID NO: 28, SEQ ID NO: 29, and SEQ ID NO: 30.
2. The fully human antibody of claim 1 , wherein the antibody comprises a heavy chain/light chain variable domain sequence selected from the group consisting of: SEQ ID NO. 1/SEQ ID NO. 2 (C47A8), SEQ ID NO. 1/SEQ ID NO. 4 (C47B10), SEQ ID NO: 1 /SEQ ID NO:8 (C47B10-1), SEQ ID NO. 1/SEQ ID NO. 5 (C47B10-1H4S), SEQ ID NO. 1/SEQ ID NO. 6 (C47B10-1F6S), SEQ ID NO. 7/SEQ ID NO. 8 (C47B10-2A9S), SEQ ID NO. 9/SEQ ID NO. 8 (C47B10-2B11S), SEQ ID NO. 10/SEQ ID NO. 4(C47B10-2B8S), SEQ ID NO. 11/SEQ ID NO. 4 (C47B10-2C1S), SEQ ID NO. 12/SEQ ID NO. 4(C47B10-2B9S), SEQ ID NO. 13/SEQ ID NO. 4 (2C4S), SEQ ID NO. 14/SEQ ID NO. 15(C47B10-B1C), SEQ ID NO. 16/SEQ ID NO. 15 (C47B10-C6C), SEQ ID NO. 17/SEQ ID NO. 15 (C47B10-D3C), SEQ ID NO. 18/SEQ ID NO. 15 (C47B10-C11C), SEQ ID NO. 19/SEQ ID NO. 15(C47B10-C11C), SEQ ID NO. 1/SEQ ID NO. 20 (C47KD8), SEQ ID NO. 1/SEQ ID NO. 21(C47KD9), SEQ ID NO:1/SEQ ID NO:8 (C47B10-1H4S2), SEQ ID NO. 32/SEQ ID NO. 15(C47B10-C3C), SEQ ID NO. 1/SEQ ID NO. 19 (C47K11), SEQ ID NO:22/SEQ ID NO:8(C47B10-H3-D4), SEQ ID NO:1/SEQ ID NO:23 (C47B10-L1A-A10), SEQ ID NO:24/SEQ ID NO:8(C47B10-H3-D3), SEQ ID NO:1/ SEQ ID NO:25 (C47B10-L1A-A4), SEQ ID NO:1/SEQ ID NO:26 (C47B10-L3-B2), SEQ ID NO:1/SEQ ID NO:27 (C47A8-CA), SEQ ID NO:1/SEQ ID NO:28 (C47A8-CL), SEQ ID NO:1/SEQ ID NO:29 (C47-A8-CQ), and SEQ ID NO:1/SEQ ID NO:30 (C47A8-CS).
3. The fully human antibody of claim 1 , wherein the antibody has a K D of at least 1×10M.
4. The antigen-binding-fragment of claim 1 , wherein the fragment comprises a heavy chain/light chain variable domain sequence selected from the group consisting of: SEQ ID NO. 1/SEQ ID NO. 2, SEQ ID NO. 1/SEQ ID NO. 4, SEQ ID NO. 1/SEQ ID NO. 5, SEQ ID NO:1/SEQ ID NO:8, SEQ ID NO. 1/SEQ ID NO. 6, SEQ ID NO. 7/SEQ ID NO. 8, SEQ ID NO. 9/SEQ ID NO. 8, SEQ ID NO. 10/SEQ ID NO. 4, SEQ ID NO. 11/SEQ ID NO. 4, SEQ ID NO. 12/SEQ ID NO. 4, SEQ ID NO. 13/SEQ ID NO. 4, SEQ ID NO. 14/SEQ ID NO. 15, SEQ ID NO. 16/SEQ ID NO. 15, SEQ ID NO. 17/SEQ ID NO. 15, SEQ ID NO. 18/SEQ ID NO. 15, SEQ ID NO. 1/SEQ ID NO. 20, SEQ ID NO. 1/SEQ ID NO. 21, SEQ ID NO. 1/SEQ ID NO. 22, SEQ ID NO:1/SEQ ID NO:8, SEQ ID NO. 32/SEQ ID NO. 15, SEQ ID NO. 1/SEQ ID NO. 19, SEQ ID NO:22/SEQ ID NO:8, SEQ ID NO:1/SEQ ID NO:23, SEQ ID NO:24/SEQ ID NO:8, SEQ ID NO:1/ SEQ ID NO:25, SEQ ID NO:1/SEQ ID NO:26, SEQ ID NO:1/SEQ ID NO:27, SEQ ID NO:1/SEQ ID NO:28, SEQ ID NO:1/SEQ ID NO:29, and SEQ ID NO:1/SEQ ID NO:30, wherein the fragment is a single chain antibody comprising a peptide linker connecting the heavy and light chain variable domains, or a Fab fragment.
5. The Fab fragment of claim 4 , wherein the antibody has a K D of at least 1×10 −6 M.
6. A method of treating CD47-associated cancer or a CD47-associated fibrotic disease in a subject in need thereof, the method comprising administering an effective amount of the antibody of claim 2 , such that the cancer is treated.
7. The method of claim 6 , wherein the cancer is selected from the group consisting of: ovarian cancer, colon cancer, breast cancer, lung cancer, myelomas, neuroblastic-derived CNS tumors, monocytic leukemias, B-cell derived leukemias, T-cell derived leukemias, B-cell derived lymphomas, T-cell derived lymphomas, and mast cell derived tumors.
8. The method of claim 6 , wherein the fibrotic disease is selected from the group consisting of myocardial infarction, angina, osteoarthritis, pulmonary fibrosis, asthma, cystic fibrosis, bronchitis, and asthma.
9. A method of treating CD47-associated cancer or a CD47-associated fibrotic disease in a subject in need thereof, the method comprising administering an effective amount of the antibody fragment of claim 4 .
10. The method of claim 9 , wherein the cancer is selected from the group consisting of: ovarian cancer, colon cancer, breast cancer, lung cancer, myelomas, neuroblastic-derived CNS tumors, monocytic leukemias, B-cell derived leukemias, T-cell derived leukemias, B-cell derived lymphomas, T-cell derived lymphomas, and mast cell derived tumors.
11. The method of claim 9 , wherein the fibrotic disease is selected from the group consisting of myocardial infarction, angina, osteoarthritis, pulmonary fibrosis, asthma, cystic fibrosis, bronchitis, and asthma.
12. The antibody, or antigen-binding fragment thereof, of claim 1 , which has a K D of at least 1×10 −6 M.
13. A pharmaceutical composition comprising the anti-CD47 antibody, or antibody fragment of claim 1 , and a pharmaceutically acceptable carrier.
14. A method of treating CD47-associated cancer or a CD47-associated fibrotic disease in a human subject in need thereof, comprising administering an effective amount of the anti-CD47 antibody, or antigen-binding fragment thereof, of claim 1 to the subject, such that cancer or the fibrotic disease is treated.
15. The method of claim 14 , wherein the cancer is selected from the group consisting of: ovarian cancer, colon cancer, breast cancer, lung cancer, myelomas, neuroblastic-derived CNS tumors, monocytic leukemias, B-cell derived leukemias, T-cell derived leukemias, B-cell derived lymphomas, T-cell derived lymphomas, and mast cell derived tumors or the fibrotic disease is selected from the group consisting of: myocardial infarction, angina, osteoarthritis, pulmonary fibrosis, asthma, cystic fibrosis, bronchitis, and asthma.