IP Library Granted Patent US 11,634,503
Granted Patent B2
US 11,634,503 · App. 16/866,408 · Granted Apr 25, 2023

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.; SEAGEN 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 11,634,503
App. No.
16/866,408
Granted
Apr 25, 2023
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 (33)

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 an amino acid sequence at least 80% homologous to the heavy chain variable region amino acid sequence set forth in SEQ ID NO:7 and a light chain variable region comprising an amino acid sequence at least 80% homologous to the light chain variable region amino acid sequence set forth in SEQ ID NO:8,

wherein the heavy chain complementarity determining region 1 (CDR-H1), CDR-H2, and CDR-H3 of the antibody or antigen binding fragment thereof are identical to the amino acid sequences of the respective CDR-H1, CDR-H2, and CDR-H3 in the heavy chain variable region sequence set forth in SEQ ID NO: 7 and the light chain complementarity determining region 1 (CDR-L1), CDR-L2, and CDR-L3 of the antibody or antigen binding fragment thereof are identical to the amino acid sequence of the respective CDR-L1, CDR-L2, and CDR-L3 in the light chain variable region sequence set forth in SEQ ID NO: 8, and

wherein the CDR-H1, CDR-H2, CDR-H3, CDR-L1, CDR-L2, and CDR-L3 are determined by Kabat numbering scheme.

2. The anti-158P1D7 antibody or antigen binding fragment thereof of claim 1 , wherein the antibody or fragment thereof comprises a heavy chain variable region comprising an amino acid sequence at least 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99% homologous to the heavy chain variable region amino acid sequence set forth in SEQ ID NO:7 and a light chain variable region comprising an amino acid sequence at least 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99% homologous to the light chain variable region amino acid sequence set forth in SEQ ID NO:8.

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

4. 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.

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

6. An antibody drug conjugate comprising the anti-158P1D7 antibody or antigen binding fragment of claim 1 conjugated to monomethyl auristatin E (MMAE) via a linker.

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

8. The antibody drug conjugate of claim 6 , wherein the linker has the formula: -Aa-Ww-Yy-; wherein -A- is a stretcher unit, a is 0 or 1; —W— is an amino acid unit, w is an integer ranging from 0 to 12; and —Y— is a spacer unit, y is 0, 1, or 2.

9. The antibody drug conjugate of claim 8 , wherein the stretcher unit has the structure of Formula I below; the amino acid unit is Val-Cit; and the spacer unit is a PAB group having the structure of Formula II below;

10. The antibody drug conjugate of claim 9 , wherein the stretcher unit forms a bond with a sulfur atom of the antibody or antigen binding fragment thereof; and wherein the spacer unit is linked to MMAE via a carbamate group.

11. The antibody drug conjugate of claim 6 , 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.

12. The antibody drug conjugate of claim 11 , wherein p ranges from 2 to 5.

13. A pharmaceutical composition comprising a therapeutically effective amount of the antibody drug conjugate of claim 11 and a pharmaceutically acceptable excipient.

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

15. The method of claim 14 , wherein the subject is a human subject.

16. The method of claim 14 , comprising administering about 1 to about 5 mg/kg of the antibody drug conjugate to the subject.

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

18. The method of claim 14 , wherein the cancer is bladder cancer.

19. A host cell selected from the group consisting of the following (a) and (b),

(a) a host cell transformed with a vector comprising a polynucleotide comprising a sequence encoding the heavy chain variable region of the antibody or antigen binding fragment as defined in claim 1 and a polynucleotide comprising a sequence encoding the light chain variable region of the antibody or antigen binding fragment as defined in claim 1 ; and

(b) a host cell transformed with a vector comprising a polynucleotide comprising a sequence encoding the heavy chain variable region of the antibody or antigen binding fragment as defined in claim 1 and a vector comprising a polynucleotide comprising a sequence encoding the light chain variable region of the antibody or antigen binding fragment as defined in claim 1 .

20. A method of producing an antibody or antigen binding fragment thereof that binds to 158P1D7, wherein the method comprises:

a) culturing the host cell of claim 19 under conditions suitable for expression of the polynucleotide encoding the antibody or antigen binding fragment thereof; and

b) isolating the antibody or antigen binding fragment thereof.

21. A method of producing an antibody drug conjugate comprising an antibody or antigen binding fragment thereof that binds to 158P1D7, wherein the method comprises:

a) culturing the host cell of claim 19 under conditions suitable for expression of the polynucleotide encoding the antibody or antigen binding fragment thereof;

b) isolating the antibody or antigen binding fragment thereof; and

c) conjugating 1 to 20 units of MMAE to the antibody or antigen binding fragment thereof, wherein each unit of MMAE is conjugated via a linker.

22. An antibody or antigen binding fragment thereof produced by the method of claim 20 .

23. An antibody drug conjugate produced by the method of claim 21 .

Assignments (1)
CHANGE OF NAME Recorded Oct 19, 2020
From: SEATTLE GENETICS, INC.
To: SEAGEN INC.
Reel/Frame 054122/0812 →
Continuity (6)
Continuation 15895996 · Feb 13, 2018
Continuation 15085877 · Mar 30, 2016
Continuation 14634606 · Feb 27, 2015
Continuation 13975214 · Aug 23, 2013
Provisional Application 61692448 · Aug 23, 2012
Related Publication 20210095043A1 · Apr 1, 2021