IP Library Granted Patent US 12,152,083
Granted Patent B2
US 12,152,083 · App. 18/099,875 · Granted Nov 26, 2024

Cytotoxic and anti-mitotic compounds, and methods of using the same

Inventors: Geoffrey C. Winters (Vancouver, CA); James R. Rich (Vancouver, CA); Graham Albert Edwin Garnett (West Vancouver, CA); Alexander Laurence Mandel (Vancouver, CA); Tom Han Hsiao Hsieh (Vancouver, CA); Elyse Marie Josée Bourque (L'Etang-du-Nord, CA); Stuart Daniel Barnscher (Langley, CA)
C07K16/2887A61K38/06A61K47/54A61K47/6813A61K47/6851A61K47/6855A61K47/6867C07K5/0205C07K16/2878C07K16/30C07K16/32H01L25/162H01L25/167H10K59/131H10K59/18H10K71/00H10K77/111A61K38/00C07K2317/24C07K2317/73H10K59/1201
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Quick Facts
Patent No.
US 12,152,083
App. No.
18/099,875
Granted
Nov 26, 2024
Kind
B2
Abstract

Compounds having cytotoxic and/or anti-mitotic activity are disclosed. Methods associated with preparation and use of such compounds, as well as pharmaceutical compositions comprising such compounds, are also disclosed. Also disclosed are compositions having the structure: (T)-(L)-(D), wherein (T) is a targeting moiety, (L) is an optional linker, and (D) is a compound having cytotoxic and/or anti-mitotic activity.

Claims (36)

1. A method of preparing a conjugate of Formula II:

(T)-(L)-(D)   II

wherein (T) is an antibody, (L) is a linker, and (D) is a compound of Formula Ig:

wherein R 2 is selected from: 4-aminobenzyl, 4-(aminomethyl)benzyl, 4-aminophenyl, 4-(aminomethyl)phenyl, 4-(1-aminocyclopropyl)benzyl and 4-(1-aminocyclopropyl)phenyl,

the method comprising:

a) preparing a drug-linker (D)-(L) comprising the compound of Formula Ig and linker (L), and

b) conjugating drug-linker (D)-(L) to antibody (T).

2. The method according to claim 1 , wherein R 2 is selected from: 4-aminobenzyl, 4-aminophenyl and 4-(1-aminocyclopropyl)phenyl.

3. The method according to claim 1 , wherein linker (L) is MT-VC-OH having the following structure:

4. The method according to claim 3 , wherein preparing drug-linker (D)-(L) comprises reacting the compound of Formula Ig with MT-VC-OH.

5. The method according to claim 3 , wherein preparing drug-linker (D)-(L) comprises:

i) reacting the compound of Formula Ig with Boc-VC-OH having the following structure:

to provide a drug-linker intermediate, and

ii) reacting the drug-linker intermediate with MT-NHS having the following structure:

6. The method according to claim 3 , wherein R 2 is selected from: 4-aminobenzyl, 4-aminophenyl and 4-(1-aminocyclopropyl)phenyl.

7. The method according to claim 3 , wherein R 2 is 4-aminophenyl.

8. The method according to claim 3 , wherein conjugating drug-linker (D)-(L) to antibody (T) comprises conjugating between 1 and 8 drug-linkers (D)-(L) to antibody (T).

9. The method according to claim 3 , wherein the antibody is a bispecific antibody.

10. The method according to claim 3 , wherein the antibody specifically binds a cancer cell antigen.

11. The method according to claim 10 , wherein the cancer cell antigen is HER2.

12. The method according to claim 1 , wherein drug-linker (D)-(L) is selected from:

13. The method according to claim 1 , wherein drug-linker (D)-(L) is:

14. The method according to claim 13 , wherein conjugating drug-linker (D)-(L) to antibody (T) comprises conjugating between 1 and 8 drug-linkers (D)-(L) to antibody (T).

15. The method according to claim 13 , wherein the antibody is a bispecific antibody.

16. The method according to claim 13 , wherein the antibody specifically binds a cancer cell antigen.

17. The method according to claim 16 , wherein the cancer cell antigen is HER2.

18. A method of preparing an antibody-drug conjugate, the method comprising conjugating a drug-linker to an antibody, the drug-linker selected from:

19. The method according to claim 18 , wherein conjugating the drug-linker to the antibody comprises conjugating between 1 and 8 drug-linkers to the antibody.

20. The method according to claim 18 , wherein the antibody is a bispecific antibody.

21. The method according to claim 18 , wherein the antibody specifically binds a cancer cell antigen.

22. The method according to claim 21 , wherein the cancer cell antigen is HER2.

23. The method according to claim 18 , wherein the drug-linker is:

24. The method according to claim 23 , wherein conjugating the drug-linker to the antibody comprises conjugating between 1 and 8 drug-linkers to the antibody.

25. The method according to claim 23 , wherein the antibody is a bispecific antibody.

26. The method according to claim 23 , wherein the antibody specifically binds a cancer cell antigen.

27. The method according to claim 26 , wherein the cancer cell antigen is HER2.

Assignments (4)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 13, 2024
From: WINTERS, GEOFFREY C.; RICH, JAMES R.; GARNETT, GRAHAM ALBERT EDWIN; MANDEL, ALEXANDER LAURENCE; HSIEH, TOM HAN HSIAO; BOURQUE, ELYSE MARIE JOSEE; BARNSCHER, STUART DANIEL
To: CENTRE FOR DRUG RESEARCH AND DEVELOPMENT
Reel/Frame 066757/0955 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 13, 2024
From: CENTRE FOR DRUG RESEARCH AND DEVELOPMENT
To: CDRD VENTURES INC.
Reel/Frame 066757/0964 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 13, 2024
From: CDRD VENTURES INC.
To: ZYMEWORKS INC.
Reel/Frame 066757/0981 →
CHANGE OF NAME Recorded Mar 13, 2024
From: ZYMEWORKS INC.
To: ZYMEWORKS BC INC.
Reel/Frame 066760/0745 →
Continuity (5)
Continuation 16523942 · Jul 26, 2019
Continuation 15872642 · Jan 16, 2018
Continuation 14857733 · Sep 17, 2015
Provisional Application 62051883 · Sep 17, 2014
Related Publication 20230317700A1 · Oct 5, 2023