IP Library › Granted Patent US 12,178,876
Granted Patent B2
US 12,178,876 · App. 18/630,197 · Granted Dec 31, 2024

Conjugates comprising cleavable linkers

Inventors: Akbar Husain Khan (Waltham, MA); Andreas Lothar Severino Maderna (Waltham, MA); Maximillian Taro William Lee (London, GB); Nicole Danielle Bartolo (Waltham, MA); William Robert Fraser Goundry (Macclesfield, GB)
Assignee: AstraZeneca, AB
A61K47/549A61K47/545A61K47/60
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Quick Facts
Patent No.
US 12,178,876
App. No.
18/630,197
Granted
Dec 31, 2024
Kind
B2
Abstract

The specification relates to conjugates comprising a linker of Formula (ICA): and pharmaceutically acceptable salts thereof. The specification also relates the use of the conjugates for the treatment of diseases such as cancer, and intermediates useful for the synthesis of the conjugates.

Claims (60)

1. A conjugate of Formula (IC)

Ab-(G A -J A -D C ) k   (IC)

or a pharmaceutically acceptable salt thereof,

wherein

Ab is an antibody or antigen-binding fragment thereof,

k is an integer from 1 to 10,

each G A is independently a conjugation group conjugated to the antibody or antigen-binding fragment thereof,

each D C is

each J A is independently a group of Formula (ICA)

E is (CH 2 ) n1 , wherein n1 is 0, 1, 2 or 3,

Q is

R 1 is C 1-4 alkyl,

X is (CH 2 ) n2 , wherein n2 is 0, 1, 2 or 3,

Y is (CH 2 ) n3 , wherein n3 is 0, 1, 2, 3 or 4,

Z is (CH 2 ) n4 , wherein n4 is 1, 2, 3, 4 or 5,

m is an integer from 5 to 17,

p is 1 or 0,

(G A ) indicates the point of attachment to G A , and

(D C ) indicates the point of attachment to D C .

2. The conjugate of Formula (IC) or a pharmaceutically acceptable salt thereof, as claimed in claim 1 , wherein Q is

3. The conjugate of Formula (IC) or a pharmaceutically acceptable salt thereof, as claimed in claim 1 , wherein m is 9, 10, 11, 12 or 13.

4. The conjugate of Formula (IC) or a pharmaceutically acceptable salt thereof, as claimed in claim 1 , wherein R 1 is CH 3 .

5. The conjugate of Formula (IC) or a pharmaceutically acceptable salt thereof, as claimed in claim 1 , wherein E is CH 2 .

6. The conjugate of Formula (IC) or a pharmaceutically acceptable salt thereof, as claimed in claim 1 , wherein X is CH 2 .

7. The conjugate of Formula (IC) or a pharmaceutically acceptable salt thereof, as claimed in claim 1 , wherein Y is (CH 2 ) 2 .

8. The conjugate of Formula (IC) or a pharmaceutically acceptable salt thereof, as claimed in claim 1 , wherein Z is (CH 2 ) 2 .

9. The conjugate of Formula (IC) or a pharmaceutically acceptable salt thereof, as claimed in claim 1 , wherein p is 1.

10. The conjugate of Formula (IC) or a pharmaceutically acceptable salt thereof, as claimed in claim 1 , wherein each J A is a group of Formula (ICB)

11. The conjugate of Formula (IC) or a pharmaceutically acceptable salt thereof, as claimed in claim 1 , wherein G A is selected from

wherein R K is H or CH 3 , R L is C 1-6 alkyl, and indicates the point of attachment to the antibody or antigen-binding fragment thereof.

12. The conjugate of Formula (IC) or a pharmaceutically acceptable salt thereof, as claimed in claim 11 , wherein G A is

13. The conjugate of Formula (IC) or a pharmaceutically acceptable salt thereof, as claimed in claim 11 , wherein G A is

14. The conjugate of Formula (IC) or a pharmaceutically acceptable salt thereof, as claimed in claim 10 , wherein G A is

wherein indicates the point of attachment to the antibody or antigen-binding fragment thereof.

15. The conjugate of Formula (IC) or a pharmaceutically acceptable salt thereof, as claimed in claim 10 , wherein G A is

wherein indicates the point of attachment to the antibody or antigen-binding fragment thereof.

16. The conjugate of Formula (IC) or a pharmaceutically acceptable salt thereof, as claimed in claim 1 , wherein k is an integer from 2 to 8.

17. A pharmaceutical composition comprising the conjugate of Formula (IC), or a pharmaceutically acceptable salt thereof, as claimed in claim 1 , and a pharmaceutically acceptable excipient.

18. A compound of Formula (IIC)

G B -J B -D C   (IIC)

or a salt thereof, wherein G B is a conjugation group for conjugation to an antibody or antigen-binding fragment thereof,

J B is a group of Formula (IICA)

wherein D C , E, Q, R 1 , X, Y, Z, m and p are as defined for a conjugate of Formula (IC) in claim 1 , (G B ) indicates the point of attachment to G B , and (D C ) indicates the point of attachment to D C .

19. The compound of Formula (IIC) or a salt thereof, as claimed in claim 18 , wherein

G B is selected from

wherein X 1 is CH or N,

h is 0 or 1,

Hal is Cl, Br or I,

R K is H or CH 3 , and

R L is C 1-6 alkyl.

20. The compound of Formula (IIC) or a salt thereof, as claimed in claim 19 , wherein

G B is

21. The compound of Formula (IIC) or a salt thereof, as claimed in claim 19 , wherein

G B is

22. The compound of Formula (IIC) or a salt thereof, as claimed in claim 18 , that is

(2S,3S,4S,5R,6S)-6-(2-((3-((S)-6-(((3 S,3aR,6S,6aR)-6-(2,5,8,11,14,17,20,23,26,29,32,35-dodecaoxaoctatriacontan-38-amido)hexahydrofuro[3,2-b]furan-3-yl)amino)-2-(3-(2,5-dioxo-2,5-dihydro-1H-pyrrol-1-yl)propanamido)-6-oxohexanamido)propanamido)methyl)-4-(((((1S,9S)-9-ethyl-5-fluoro-9-hydroxy-4-methyl-10,13-dioxo-2,3,9,10,13,15-hexahydro-1H,12H-benzo[de]pyrano[3′,4′:6,7]indolizino[1,2-b]quinolin-1-yl)carbamoyl)oxy)methyl)phenoxy)-3,4,5-trihydroxytetrahydro-2H-pyran-2-carboxylic acid, or a salt thereof.

23. The compound of Formula (IIC) or a salt thereof, as claimed in claim 18 , that is

(2S,3S,4S,5R,6S)-6-(2-((S)-8-(4-(((3S,3aR,6S,6aR)-6-(2,5,8,11,14,17,20,23,26,29,32,35-dodecaoxaoctatriacontan-38-amido)hexahydrofuro[3,2-b]furan-3-yl)amino)-4-oxobutyl)-15-bromo-3,7,10,14-tetraoxo-2,6,9,13-tetraazapentadecyl)-4-(((((1S,9S)-9-ethyl-5-fluoro-9-hydroxy-4-methyl-10,13-dioxo-2,3,9,10,13,15-hexahydro-1H,12H-benzo[de]pyrano[3′,4′:6,7]indolizino-[1,2-b]quinolin-1-yl)carbamoyl)oxy)methyl)phenoxy)-3,4,5-trihydroxytetrahydro-2H-pyran-2-carboxylic acid, or a salt thereof.

24. A compound of Formula (IXC)

or a salt thereof, wherein G B is a conjugation group for conjugation to an antibody or antigen-binding fragment thereof, and E, Y, Z and p are as defined for a conjugate of Formula (IC) in claim 1 , R Q1 is H or R P1 , each R Q2 is independently H or R P2 and R Q3 is H or R P3 , wherein R P1 is a carboxylic acid protecting group, each R P2 is independently an alcohol protecting group and R P3 is an amine protecting group.

Assignments (4)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 24, 2025
From: KHAN, AKBAR HUSAIN; MADERNA, ANDREAS LOTHAR SEVERINO; BARTOLO, NICOLE DANIELLE
To: ASTRAZENECA PHARMACEUTICALS LP
Reel/Frame 072670/0712 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 24, 2025
From: GOUNDRY, WILLIAM ROBERT FRASER; LEE, MIXIMILLIAN TARO WILLIAM
To: ASTRAZENECA UK LIMITED
Reel/Frame 072671/0072 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 24, 2025
From: ASTRAZENECA PHARMACEUTICALS LP
To: ASTRAZENECA UK LIMITED
Reel/Frame 072671/0138 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 24, 2025
From: ASTRAZENECA UK LIMITED
To: ASTRAZENECA AB
Reel/Frame 072671/0261 →
Continuity (2)
Provisional Application 63496709 · Apr 18, 2023
Related Publication 20240366768A1 · Nov 7, 2024