Antibody drug conjugates (ADC) that bind to 158P1D7 proteins
View Patent ↗Antibody drug conjugates (ADC's) that bind to 158P1D7 protein and variants thereof are described herein. 158P1D7 exhibits tissue specific expression in normal adult tissue, and is aberrantly expressed in glioblastoma, lung cancer, bladder cancer, and breast cancer. Consequently, the ADC's of the invention provide a therapeutic composition for the treatment of cancer.
1. An antibody drug conjugate comprising an antibody or antigen binding fragment which binds to a 158P1D7 protein, wherein the antibody or antigen binding fragment is conjugated to monomethyl auristatin E (MMAE), and wherein the antibody or fragment comprises a heavy chain variable region consisting of the amino acid sequence ranging from position 1 to position 120 of SEQ ID NO: 7 and a light chain variable consisting of the amino acid sequence ranging from position 1 to position 113 of SEQ ID NO: 8.
2. The antibody drug conjugate of claim 1 , wherein the antibody comprises a heavy chain consisting of the amino acid sequence ranging from position 1 to position 446 of SEQ ID NO: 7 and a light chain consisting of the amino acid sequence ranging from position 1 to position 219 of SEQ ID NO: 8.
3. An antibody drug conjugate comprising an antibody or antigen binding fragment which binds to a 158P1D7 protein, wherein the antibody or antigen binding fragment is conjugated to monomethyl auristatin E (MMAE), wherein the antibody or fragment comprises a heavy chain variable region consisting of the amino acid sequence of the heavy chain variable region of an antibody produced by a Chinese Hamster Ovary (CHO) cell deposited under American Type Culture Collection (ATCC) Accession No. PTA-13102, and a light chain variable region consisting of the amino acid sequence of the light chain variable region of an antibody produced by a Chinese Hamster Ovary (CHO) cell deposited under ATCC Accession No. PTA-13102.
4. The antibody drug conjugate of claim 3 , wherein the antibody comprises a heavy chain consisting of the amino acid sequence of the heavy chain of an antibody produced by a Chinese Hamster Ovary (CHO) cell deposited under ATCC. Accession No. PTA-13102, and a light chain consisting of the amino acid sequence of a light chain of an antibody produced by a Chinese Hamster Ovary (CHO) deposited under ATCC. Accession No. PTA-13102.
5. The antibody drug conjugate of claim 1 , wherein the fragment is an Fab, F(ab') 2 , Fv or scFv fragment.
6. The antibody drug conjugate of claim 1 , wherein the antibody is a fully human antibody.
7. The antibody drug conjugate of claim 1 , which the antibody is recombinantly produced.
8. A pharmaceutical composition that comprises the antibody drug conjugate of claim 1 in a human unit dose form.
9. The pharmaceutical composition of claim 8 , wherein the composition is for treatment of glioblastoma cancer, lung cancer, bladder cancer, or breast cancer.
10. The pharmaceutical composition of claim 8 , wherein the composition is administered in combination with radiation or a chemotherapeutic agent.
11. The pharmaceutical composition of claim 8 , further comprising a chemotherapeutic agent in a human unit dose form.
12. A method of treating bladder cancer in a subject, comprising administering to said subject an antibody drug conjugate of claim 1 .
13. A method for treating bladder cancer in a subject, comprising administering to said subject an effective amount of a combination of an antibody drug conjugate of claim 1 and radiation.
14. A method for treating bladder cancer in a subject, comprising administering to said subject an effective amount of a combination of an antibody drug conjugate of claim 1 and a chemotherapeutic agent.
15. An anti-158P1D7 antibody or antigen binding fragment thereof, wherein the antibody or antigen binding fragment thereof comprises a heavy chain variable region comprising complementarity determining regions (CDRs) consisting of the amino acid sequences of the CDRs in the heavy chain variable region sequence set forth in SEQ ID NO:7 and a light chain variable region comprising CDRs consisting of the amino acid sequences of the CDRs in the light chain variable region sequence set forth in SEQ ID NO:8.
16. The antibody or antigen binding fragment of claim 15 , wherein the antibody or antigen binding fragment thereof comprises a heavy chain variable region consisting of the amino acid sequence ranging from position 1 to position 120 of SEQ ID NO:7 and a light chain variable region consisting of the amino acid sequence ranging from position 1 to position 113 of SEQ ID NO:8.
17. The antibody or antigen binding fragment of claim 15 , wherein the fragment is an Fab, F(ab') 2 , Fv or scFv fragment.
18. The antibody or antigen binding fragment of claim 15 further comprising a human IgG constant region and a human light chain constant region.
19. The antibody or antigen binding fragment of claim 18 , wherein the IgG constant region is IgG2 and the light chain constant region is kappa.
20. The antibody or antigen binding fragment of claim 19 , wherein the antibody or antigen binding fragment comprises a heavy chain consisting of the amino acid sequence ranging from position 1 to position 446 of SEQ ID NO:7 and a light chain consisting of the amino acid sequence ranging from position 1 to position 219 of SEQ ID NO:8.
21. The antibody or antigen binding fragment of claim 15 , wherein the antibody is a fully human antibody.
22. The antibody or antigen binding fragment of claims 15 , wherein the antibody is recombinantly produced.
23. An antibody drug conjugate comprising the antibody or antibody binding fragment of claim 15 conjugated to a cytotoxic agent.
24. The antibody drug conjugate of claim 23 , wherein the cytotoxic agent is monomethyl auristatin E (MMAE).
25. The antibody drug conjugate of claim 24 , wherein the antibody drug conjugate has the following structure:
wherein Ab-s- represents anti-158P1D7 antibody and p ranges from 1 to about 10.
26. A pharmaceutical composition that comprises the antibody drug conjugate of claim 23 in a human unit dose form.
27. The pharmaceutical composition of claim 26 , wherein the composition is for bladder cancer treatment.
28. The pharmaceutical composition of claim 27 , wherein the composition is administered in combination with radiation or a chemotherapeutic agent.
29. The pharmaceutical composition of claim 28 , further comprising a chemotherapeutic agent in a human unit dose form.
30. A method of treating bladder cancer in a subject, comprising administering to said subject an antibody drug conjugate of claim 23 .
31. A method for treating bladder cancer in a subject, comprising administering to said subject an effective amount of a combination of an antibody drug conjugate of claim 24 and radiation.
32. A method for treating bladder cancer in a subject, comprising administering to said subject an effective amount of a combination of an antibody drug conjugate of claim 25 and a chemotherapeutic agent.