IP Library Granted Patent US 9,133,271
Granted Patent B1
US 9,133,271 · App. 14/742,576 · Granted Sep 15, 2015

Anti-DLL3 antibody drug conjugates and methods of use

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Quick Facts
Patent No.
US 9,133,271
App. No.
14/742,576
Granted
Sep 15, 2015
Kind
B1
Abstract

Provide are novel modulators, including antibodies and derivatives thereof, and methods of using such modulators to treat recurrent tumors and to reduce or inhibit tumor recurrence in a subject.

Claims (46)

1. A method of treating a recurrent tumor in a subject, the method comprising administering to the subject a therapeutically effective amount of an anti-DLL3 antibody drug conjugate (ADC), or a pharmaceutically acceptable salt thereof, wherein the antibody drug conjugate (ADC) comprises the formula M-[L-D]n, wherein:

M comprises an anti-DLL3 antibody;

L comprises an optional linker;

D comprises a cytotoxic agent; and

n is an integer from 1 to 20.

2. The method of claim 1 , wherein the recurrent tumor comprises lung cancer.

3. The method of claim 2 , wherein the recurrent tumor comprises small cell lung cancer.

4. The method of claim 2 , wherein the recurrent tumor comprises non-small cell lung cancer.

5. The method of claim 2 , wherein the lung cancer is refractory, relapsed or resistant to a platinum based agent and/or a taxane.

6. The method of claim 1 , wherein the subject has previously undergone a debulking procedure.

7. The method of claim 1 , wherein M comprises an anti-DLL3 antibody that specifically binds to an epitope within the DSL domain of a DLL3 protein set forth as SEQ ID NO: 3 or 4.

8. The method of claim 1 , wherein the anti-DLL3 antibody specifically binds to an epitope comprising amino acids G203, R205 and P206 (SEQ ID NO: 10).

9. The method of claim 1 , wherein the anti-DLL3 antibody is a chimeric antibody, a CDR-grafted antibody, or a humanized antibody.

10. The method of claim 1 , wherein the anti-DLL3 antibody competes for binding to human DLL3 protein with an antibody comprising a light chain variable region set forth as SEQ ID NO: 84 and a heavy chain variable region set forth as SEQ ID NO: 85.

11. The method of claim 1 , wherein the anti-DLL3 antibody comprises residues 24-34 of SEQ ID NO: 84 for CDR-L1, residues 50-56 of SEQ ID NO: 84 for CDR-L2, residues 89-97 of SEQ ID NO: 84 for CDR-L3, residues 31-35 of SEQ ID NO: 85 for CDR-H1, residues 50-65 of SEQ ID NO: 85 for CDR-H2 and residues 95-102 of SEQ ID NO: 85 for CDR-H3, wherein the residues are numbered according to Kabat.

12. The method of claim 11 , wherein D comprises a pyrrolobenzodiazepine (PBD).

13. The method of claim 1 , wherein the anti-DLL3 antibody comprises a light chain variable region comprising an amino acid sequence set forth as SEQ ID NO: 212 and a heavy chain variable region comprising an amino acid sequence set forth as SEQ ID NO: 213.

14. The method of claim 1 , wherein D comprises a pyrrolobenzodiazepine (PBD).

15. A method of reducing or inhibiting tumor recurrence in a subject, the method comprising administering to the subject a therapeutically effective amount of an anti-DLL3 antibody drug conjugate (ADC), or a pharmaceutically acceptable salt thereof, wherein the antibody drug conjugate (ADC) comprises the formula M-[L-D]n, wherein:

M comprises an anti-DLL3 antibody;

L comprises an optional linker;

D comprises a cytotoxic agent; and

n is an integer from 1 to 20.

16. The method of claim 15 , wherein the recurrent tumor comprises lung cancer.

17. The method of claim 15 , wherein the recurrent tumor comprises small cell lung cancer.

18. The method of claim 15 , wherein the recurrent tumor comprises non-small cell lung cancer.

19. The method of claim 15 , wherein the lung cancer is refractory, relapsed or resistant to a platinum based agent and/or a taxane.

20. The method of claim 15 , wherein the subject has previously undergone a debulking procedure.

21. The method of claim 15 , wherein M comprises an anti-DLL3 antibody that specifically binds to an epitope within the DSL domain of a DLL3 protein set forth as SEQ ID NO: 3 or 4.

22. The method of claim 15 , wherein the anti-DLL3 antibody specifically binds to an epitope comprising amino acids G203, R205 and P206 (SEQ ID NO: 10).

23. The method of claim 15 , wherein the anti-DLL3 antibody is a chimeric antibody, a CDR-grafted antibody, or a humanized antibody.

24. The method of claim 15 , wherein the anti-DLL3 antibody competes for binding to human DLL3 protein with an antibody comprising a light chain variable region set forth as SEQ ID NO: 84 and a heavy chain variable region set forth as SEQ ID NO: 85.

25. The method of claim 15 , wherein the anti-DLL3 antibody comprises residues 24-34 of SEQ ID NO: 84 for CDR-L1, residues 50-56 of SEQ ID NO: 84 for CDR-L2, residues 89-97 of SEQ ID NO: 84 for CDR-L3, residues 31-35 of SEQ ID NO: 85 for CDR-H1, residues 50-65 of SEQ ID NO: 85 for CDR-H2 and residues 95-102 of SEQ ID NO: 85 for CDR-H3, wherein the residues are numbered according to Kabat.

26. The method of claim 25 , wherein D comprises a pyrrolobenzodiazepine (PBD).

27. The method of claim 15 , wherein the anti-DLL3 antibody comprises a light chain variable region comprising an amino acid sequence set forth as SEQ ID NO: 212 and a heavy chain variable region comprising an amino acid sequence set forth as SEQ ID NO: 213.

28. The method of claim 15 , wherein D comprises a pyrrolobenzodiazepine (PBD).

29. A method of treating lung cancer in a subject, wherein the lung cancer is refractory, relapsed or resistant to a platinum based agent and/or a taxane, the method comprising administering to the subject a therapeutically effective amount of an anti-DLL3 antibody drug conjugate (ADC), or a pharmaceutically acceptable salt thereof, wherein the antibody drug conjugate (ADC) comprises the formula M-[L-D]n, wherein:

M comprises an anti-DLL3 antibody, wherein the anti-DLL3 antibody comprises residues 24-34 of SEQ ID NO: 84 for CDR-L1, residues 50-56 of SEQ ID NO: 84 for CDR-L2, residues 89-97 of SEQ ID NO: 84 for CDR-L3, residues 31-35 of SEQ ID NO: 85 for CDR-H1, residues 50-65 of SEQ ID NO: 85 for CDR-H2 and residues 95-102 of SEQ ID NO: 85 for CDR-H3, wherein the residues are numbered according to Kabat;

L comprises a linker;

D comprises a pyrrolobenzodiazepine (PBD); and

n is an integer from 1 to 20.

30. A method of treating cancer in a subject, wherein the subject has previously had a debulking procedure, the method comprising administering to the subject a therapeutically effective amount of an anti-DLL3 antibody drug conjugate (ADC), or a pharmaceutically acceptable salt thereof, wherein the antibody drug conjugate (ADC) comprises the formula M-[L-D]n, wherein:

M comprises an anti-DLL3 antibody, wherein the anti-DLL3 antibody comprises residues 24-34 of SEQ ID NO: 84 for CDR-L1, residues 50-56 of SEQ ID NO: 84 for CDR-L2, residues 89-97 of SEQ ID NO: 84 for CDR-L3, residues 31-35 of SEQ ID NO: 85 for CDR-H1, residues 50-65 of SEQ ID NO: 85 for CDR-H2 and residues 95-102 of SEQ ID NO: 85 for CDR-H3, wherein the residues are numbered according to Kabat;

L comprises a linker;

D comprises a pyrrolobenzodiazepine (PBD); and

n is an integer from 1 to 20.

Assignments (3)
MERGER Recorded Aug 7, 2016
From: STEMCENTRX, INC.
To: ABBVIE STEMCENTRX LLC
Reel/Frame 039601/0189 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 9, 2015
From: STULL, ROBERT A; SAUNDERS, LAURA; DYLLA, SCOTT J.; FOORD, ORIT; LIU, DAVID; TORGOV, MICHAEL; SHAO, HUI
To: STEM CENTRX, INC.
Reel/Frame 036049/0570 →
CHANGE OF NAME Recorded Jul 9, 2015
From: STEM CENTRX, INC.
To: STEMCENTRX, INC.
Reel/Frame 036087/0967 →