IP Library Granted Patent US 9,770,518
Granted Patent B1
US 9,770,518 · App. 15/608,988 · Granted Sep 26, 2017

Anti-DLL3 antibody drug conjugates

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Quick Facts
Patent No.
US 9,770,518
App. No.
15/608,988
Granted
Sep 26, 2017
Kind
B1
Abstract

Novel modulators, including antibodies and derivatives thereof, and methods of using such modulators to treat proliferative disorders are provided.

Claims (92)

1. An antibody drug conjugate of the formula M-[L-D]n, or a pharmaceutically acceptable salt thereof, wherein:

M comprises a humanized anti-DLL3 antibody comprising a light chain variable region set forth as SEQ ID NO: 212 and a heavy chain variable region set forth as SEQ ID NO: 213;

L comprises a linker;

D comprises a pyrrolobenzodiazepine (PBD) comprising the formula AC:

wherein:

the dotted lines indicate the optional presence of a double bond, and wherein only one of the dotted lines in a given ring can be a double bond;

R 2 is selected from H, OH, ═O, ═CH 2 , CN, R, OR, ═CH—R D , ═C(R D ) 2 , OSO 2 R, CO 2 R, COR, and halo, where R D is selected from R, CO 2 R, COR, CHO, CO 2 H, and halo;

R 6 and R 9 are each independently selected from H, R, OH, OR, SH, SR, NH 2 , NHR, NRR′, NO 2 , Me 3 Sn and halo;

R 7 is selected from H, R, OH, OR, SH, SR, NH 2 , NHR, NRR′, NO 2 , Me 3 Sn and halo;

R 10 is the linker connected to the anti-DLL3 antibody;

Q is selected from 0, S and NH;

R 11 is either H, or R or, where Q is O, SO 3 M, where M is a metal cation;

R and R′ are each independently selected from optionally substituted C 1-12 alkyl, C 3-20 heterocyclyl and C 5-20 aryl groups, and optionally in relation to the group NRR′, R and R′ together with the nitrogen atom to which they are attached form an optionally substituted 4-, 5-, 6- or 7-membered heterocyclic ring;

X is selected from O, S, and N(H);

R 2″ , R 6″ , R 7″ , R 9″ , and X″ are as defined according to R 2 , R 6 , R 7 , R 9 , and X, respectively; and

R″ is a C 3-12 alkylene group, which comprises a chain optionally interrupted by one or more heteroatoms, one or more rings, or both one or more heteroatoms and one or more rings, wherein the optional one or more rings are optionally substituted; and

n is an integer from 1 to 20.

2. The antibody drug conjugate of claim 1 comprising the structure:

wherein:

CBA is a cell binding agent, which is the anti-DLL3 antibody M;

A, L 1 , and L 2 are components of the linker L;

A is a connecting group connecting L 1 to the cell binding agent (CBA);

L 1 is optionally a cleavable linker;

L 2 is a covalent bond or together with the —OC(═O)— group forms a self-immolative linker; and

wherein the linker L is attached to the pyrrolobenzodiazepine (PBD) at the position of the asterisk (*).

3. The antibody drug conjugate of claim 2 , wherein the L 1 comprises a cleavable linker.

4. The antibody drug conjugate of claim 3 , wherein the cleavable linker comprises a dipeptide.

5. The antibody drug conjugate of claim 4 , wherein the dipeptide is Phe-Lys, Val-Ala, Val-Lys, Ala-Lys, Val-Cit, Phe-Cit, Leu-Cit, Ile-Cit, Phe-Arg, or Trp-Cit.

6. The antibody drug conjugate of claim 5 , wherein the dipeptide is Val-Ala.

7. The antibody drug conjugate of claim 2 , wherein the moiety:

 comprises the structure:

wherein the wavy line indicates the point of attachment of the structure directly to A or to a remaining portion of L 1 that is further connected to A.

8. The antibody drug conjugate of claim 1 , wherein:

R 2 is R, wherein R is a C 5-20 aryl group;

R 6 and R 9 are H;

R 7 is OR, and wherein R is a C 1 alkyl;

Q is O, and wherein R 11 is H; and/or

X and X″ are O.

9. The antibody drug conjugate of claim 8 , wherein R 2 is R, wherein R is a C 5-20 aryl group.

10. The antibody drug conjugate of claim 8 , wherein R 6 and R 9 are H.

11. The antibody drug conjugate of claim 8 , wherein R 7 is OR.

12. The antibody drug conjugate of claim 11 , wherein R is a C 1 alkyl.

13. The antibody drug conjugate of claim 8 , wherein Q is O.

14. The antibody drug conjugate of claim 13 , wherein R 11 is H.

15. The antibody drug conjugate of claim 8 , wherein X and X″ are O.

16. A pharmaceutical composition comprising:

(a) an antibody drug conjugate of the formula M-[L-D]n, or a pharmaceutically acceptable salt thereof, wherein:

M comprises a humanized anti-DLL3 antibody comprising a light chain variable region set forth as SEQ ID NO: 212 and a heavy chain variable region set forth as SEQ ID NO: 213;

L comprises a linker;

D comprises a pyrrolobenzodiazepine (PBD) comprising the formula AC:

wherein:

the dotted lines indicate the optional presence of a double bond, and wherein only one of the dotted lines in a given ring can be a double bond;

R 2 is selected from H, OH, ═O, ═CH 2 , CN, R, OR, ═CH—R D , ═C(R D ) 2 , OSO 2 R, CO 2 R, COR, and halo, where R D is selected from R, CO 2 R, COR, CHO, CO 2 H, and halo;

R 6 and R 9 are each independently selected from H, R, OH, OR, SH, SR, NH 2 , NHR, NRR′, NO 2 , Me 3 Sn and halo;

R 7 is selected from H, R, OH, OR, SH, SR, NH 2 , NHR, NRR′, NO 2 , Me 3 Sn and halo;

R 10 is the linker connected to the anti-DLL3 antibody;

Q is selected from 0, S and NH;

R 11 is either H, or R or, where Q is O, SO 3 M, where M is a metal cation;

R and R′ are each independently selected from optionally substituted C 1-12 alkyl, C 3-20 heterocyclyl and C 5-20 aryl groups, and optionally in relation to the group NRR′, R and R′ together with the nitrogen atom to which they are attached form an optionally substituted 4-, 5-, 6- or 7-membered heterocyclic ring;

X is selected from O, S, and N(H);

R 2″ , R 6″ , R 7″ , R 9″ , and X″ are as defined according to R 2 , R 6 , R 7 , R 9 , and X, respectively; and

R″ is a C 3-12 alkylene group, which comprises a chain optionally interrupted by one or more heteroatoms, one or more rings, or both one or more heteroatoms and one or more rings, wherein the optional one or more rings are optionally substituted; and

n is an integer from 1 to 20; and

(b) a pharmaceutically acceptable carrier.

17. The pharmaceutical composition of claim 16 , wherein the antibody drug conjugate comprises the structure:

wherein:

CBA is a cell binding agent, which is the anti-DLL3 antibody M;

A, L 1 , and L 2 are components of the linker L;

A is a connecting group connecting L 1 to the cell binding agent (CBA);

L 1 is optionally a cleavable linker;

L 2 is a covalent bond or together with the —OC(═O)— group forms a self-immolative linker; and

wherein the linker L is attached to the pyrrolobenzodiazepine (PBD) at the position of the asterisk (*).

18. The pharmaceutical composition of claim 17 , wherein L 1 comprises a cleavable linker.

19. The pharmaceutical composition of claim 18 , wherein the cleavable linker comprises a dipeptide.

20. The pharmaceutical composition of claim 19 , wherein the dipeptide is Phe-Lys, Val-Ala, Val-Lys, Ala-Lys, Val-Cit, Phe-Cit, Leu-Cit, Ile-Cit, Phe-Arg, or Trp-Cit.

21. The pharmaceutical composition of claim 20 , wherein the dipeptide is Val-Ala.

22. The pharmaceutical composition of claim 17 , wherein the moiety:

 comprises the structure:

wherein the wavy line indicates the point of attachment of the structure directly to A or to a remaining portion of L 1 that is further connected to A.

23. The pharmaceutical composition of claim 16 , wherein:

R 2 is R, wherein R is a C 5-20 aryl group;

R 6 and R 9 are H;

R 7 is OR, and wherein R is a C 1 alkyl;

Q is O, and wherein R 11 is H; and/or

X and X″ are O.

24. The pharmaceutical composition of claim 23 , wherein R 2 is R, wherein R is a C 5-20 aryl group.

25. The pharmaceutical composition of claim 23 , wherein R 6 and R 9 are H.

26. The pharmaceutical composition of claim 23 , wherein R 7 is OR.

27. The pharmaceutical composition of claim 26 , wherein R is a C 1 alkyl.

28. The pharmaceutical composition of claim 23 , wherein Q is O.

29. The pharmaceutical composition of claim 28 , wherein R 11 is H.

30. The pharmaceutical composition of claim 23 , wherein X and X″ are O.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 2, 2017
From: STULL, ROBERT A.; SAUNDERS, LAURA; DYLLA, SCOTT J.; FOORD, ORIT; LIU, DAVID; TORGOV, MICHAEL; SHAO, HUI
To: STEM CENTRX, INC.
Reel/Frame 042579/0477 →
MERGER Recorded Jun 2, 2017
From: STEMCENTRX, INC.
To: ABBVIE STEMCENTRX LLC
Reel/Frame 042579/0497 →
CHANGE OF NAME Recorded Jun 2, 2017
From: STEM CENTRX, INC.
To: STEMCENTRX, INC.
Reel/Frame 042676/0011 →