IP Library Granted Patent US 10,669,348
Granted Patent B2
US 10,669,348 · App. 15/895,996 · Granted Jun 2, 2020

Antibody drug conjugates (ADC) that bind to 158P1D7 proteins

Inventors: Robert Kendall Morrison (Santa Monica, CA); Zili An (Santa Monica, CA); Karen Jane Meyrick Morrison (Santa Monica, CA); Josh Snyder (Santa Monica, CA); Xiao-Chi Jia (Los Angeles, CA)
Assignees: AGENSYS, INC.; SEATTLE GENETICS, INC.
C07K16/30A61K45/06A61K47/6803A61K47/6811A61K47/6813A61K47/6817A61K47/6849A61K47/6851A61K47/6855A61K47/6857A61K47/6859A61K47/6861A61K47/6865A61P35/00C07K16/18C07K16/3015C07K16/3023C07K16/3038C07K16/3053A61K2039/505C07K2317/21C07K2317/56C07K2317/73C07K2317/76C07K2317/77C07K2317/92
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Quick Facts
Patent No.
US 10,669,348
App. No.
15/895,996
Granted
Jun 2, 2020
Kind
B2
Abstract

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.

Claims (32)

1. 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 set forth in SEQ ID NO: 7 according to Kabat numbering and a light chain variable region consisting of the amino acid sequence ranging from position 1 to position 113 of SEQ ID NO: 8.

2. The antigen binding fragment thereof of claim 1 , wherein the antigen binding fragment is an Fab, F(ab′)2, Fv, or scFv fragment.

3. The anti-158P1D7 antibody or antigen binding fragment thereof of claim 1 , wherein the antibody or antigen binding fragment thereof is a fully human antibody or antigen binding fragment thereof.

4. The anti-158P1D7 antibody or antigen binding fragment thereof of claim 1 , wherein the antibody or antigen binding fragment thereof is recombinantly produced.

5. An antibody drug conjugate comprising the antibody or antibody binding fragment of claim 1 conjugated to monomethyl auristatin E (MMAE) via a linker.

6. The antibody drug conjugate of claim 5 , wherein the linker comprises valine-citrulline.

7. The antibody drug conjugate of claim 5 , wherein the antibody drug conjugate has the following structure:

wherein L- represents the antibody or antigen binding fragment thereof and p ranges from 1 to 10.

8. The antibody drug conjugate of claim 7 , wherein the p ranges from 2 to 5.

9. A pharmaceutical composition comprising a therapeutically effective amount of the antibody drug conjugate of claim 7 and a pharmaceutically acceptable excipient.

10. The pharmaceutical composition of claim 9 , wherein the composition is in a human unit dose form.

11. A method of treating cancer in a subject, comprising administering to said subject a therapeutically effective amount of the antibody drug conjugate of claim 7 , wherein the cancer expresses 158P1D7.

12. The method of claim 11 , wherein the subject is a human subject.

13. The method of claim 11 , comprising administering about 1 to about 5 mg/kg of the antibody drug conjugate to the subject.

14. The method of claim 11 , wherein the cancer is selected from the group consisting of glioblastoma, lung cancer, bladder cancer, and breast cancer.

15. The method of claim 11 , wherein the cancer is bladder cancer.

16. An anti-158P1D7 antibody or antigen binding fragment thereof, 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 comprising CDRs consisting of the amino acid sequences of the CDRs set forth in SEQ ID NO: 8 according to Kabat numbering.

17. The antigen binding fragment thereof of claim 16 , wherein the antigen binding fragment is an Fab, F(ab′)2, Fv, or scFv fragment.

18. The anti-158P1D7 antibody or antigen binding fragment thereof of claim 16 , wherein the antibody or antigen binding fragment thereof is a fully human antibody or antigen binding fragment thereof.

19. The anti-158P1D7 antibody or antigen binding fragment thereof of claim 16 , wherein the antibody or antigen binding fragment thereof is recombinantly produced.

20. An antibody drug conjugate comprising the antibody or antibody binding fragment of claim 16 conjugated to monomethyl auristatin E (MMAE) via a linker.

21. The antibody drug conjugate of claim 20 , wherein the linker comprises valine-citrulline.

22. The antibody drug conjugate of claim 20 , wherein the antibody drug conjugate has the following structure:

wherein L- represents the antibody or antigen binding fragment thereof and p ranges from 1 to 10.

23. The antibody drug conjugate of claim 22 , wherein the p ranges from 2 to 5.

24. A pharmaceutical composition comprising a therapeutically effective amount of the antibody drug conjugate of claim 22 and a pharmaceutically acceptable excipient.

25. The pharmaceutical composition of claim 24 , wherein the composition is in a human unit dose form.

26. A method of treating cancer in a subject, comprising administering to said subject a therapeutically effective amount of the antibody drug conjugate of claim 20 , wherein the cancer expresses 158P1D7.

27. The method of claim 26 , wherein the subject is a human subject.

28. The method of claim 27 , comprising administering about 1 to about 5 mg/kg of the antibody drug conjugate to the subject.

29. The method of claim 27 , wherein the cancer is selected from the group consisting of glioblastoma, lung cancer, bladder cancer, and breast cancer.

30. The method of claim 29 , wherein the cancer is bladder cancer.

Assignments (1)
CHANGE OF NAME Recorded Feb 22, 2021
From: SEATTLE GENETICS, INC.
To: SEAGEN INC.
Reel/Frame 055362/0182 →
Cited By (1)
US 12,194,321