IP Library › Granted Patent US 12,514,926
Granted Patent B2
US 12,514,926 · App. 18/581,307 · Granted Jan 6, 2026

Splicing modulator antibody-drug conjugates and methods of use

Inventors: Ermira Pazolli (Wayland, MA); Silvia Buonamici (Boston, MA); Thiwanka Samarakoon (Westwood, MA); Sudeep Prajapati (Somerville, MA); Nathan Fishkin (Weymouth, MA); James Palacino (Wellesley, MA); Michael Seiler (Belmont, MA); Ping Zhu (Acton, MA); Andrew Cook (Stow, MA); Peter Smith (Arlington, MA); Xiang Liu (Winchester, MA); Shelby Ellery (Boston, MA); Dominic Reynolds (Stoneham, MA); Lihua Yu (Acton, MA); Zhenhua Wu (Belmont, MA); Shouyong Peng (Belmont, MA); Nicholas Calandra (Boston, MA); Megan Sheehan (Allston, MA); Yonghong Xiao (Belmont, MA)
Assignee: EISAI R&D MANAGEMENT CO., LTD.
A61K47/6803A61K9/127A61K9/51A61K31/365A61K31/496A61K39/0011A61K39/3955A61K39/39558A61K45/06A61K47/60A61K47/6845A61K47/6849A61K47/6851A61K47/6857A61K47/6869A61K47/6871A61K47/6889A61P35/00C07D313/00C07D405/06C07D405/12C07K16/24C07K16/28C07K16/2803C07K16/2818C07K16/2827C07K16/2896C07K16/3007C07K16/3092C07K16/32C07K16/40C12Q1/6886G01N33/5011G01N33/574A61K39/00A61K2039/505A61K2039/53A61K2039/545C07K2317/565C07K2317/76C12Q2600/106G01N2500/10
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Quick Facts
Patent No.
US 12,514,926
App. No.
18/581,307
Granted
Jan 6, 2026
Kind
B2
Abstract

Linker-drug compounds and antibody-drug conjugates that bind to human oncology targets are disclosed. The linker-drug compounds and antibody-drug conjugates comprise a splicing modulator drug moiety. The disclosure further relates to methods and compositions for use in the treatment of neoplastic disorders by administering the antibody-drug conjugates provided herein. In an embodiment, the splicing modulator comprises a pladienolide or a pladienolide derivative.

Claims (56)

1 . A compound of Formula (VI-A):

or a pharmaceutically acceptable salt thereof, wherein:

R 1 and R 9 are each independently chosen from absent, hydrogen, C 1 -C 6 alkyl groups, C 1 -C 6 alkylalkoxy groups, C 1 -C 6 alkylamino groups, C 1 -C 6 alkylcarboxylic acid groups, C 1 -C 6 alkylhydroxy groups, C 3 -C 8 cycloalkyl groups, benzyl groups, C 3 -C 8 heterocyclyl groups, —O—C(=O)—(C 1 -C 6 alkyl) groups, and —CD 3 ;

R 3 is chosen from hydrogen, C 1 -C 6 alkyl groups, C 1 -C 6 alkylalkoxy groups, C 1 -C 6 alkylamino groups, C 1 -C 6 alkylcarboxylic acid groups, C 1 -C 6 alkylhydroxy groups, C 3 -C 8 cycloalkyl groups, benzyl groups, C 3 -C 8 heterocyclyl groups, and —O—C(=O)—(C 1 -C 6 alkyl) groups;

R 4 , R 5 , and R 8 are each independently chosen from hydrogen, hydroxyl, —O—(C 1 -C 6 alkyl) groups, —O—C(=O)—(C 1 -C 6 alkyl) groups, and C 1 -C 6 alkyl groups;

R 6 and R 7 are each independently chosen from hydrogen, —O—R 17 , —O—C(=O)—R 17 , —O—C(=O)—NR 15 R 16 , C 1 -C 6 alkyl groups, and —NR 15 R 16 ;

R 10 is chosen from hydrogen, C 1 -C 6 alkyl groups, —C(=O)—(C 1 -C 6 alkyl) groups, and —CD 3 ;

R 15 and R 16 are each independently chosen from hydrogen, R 17 , —C(=O)—R 17 , and —C(=O)—O—R 17 ;

R 17 is chosen from hydrogen, C 1 -C 6 alkyl groups, C 3 -C 8 cycloalkyl groups, benzyl groups, and C 3 -C 8 heterocyclyl groups; and

a is 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10;

wherein R 1 , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , R 9 , and R 10 are each independently substituted with 0 to 3 groups independently chosen from halogens, hydroxyl, C 1 -C 6 alkyl groups, —O—(C 1 -C 6 alkyl) groups, —NR 15 R 16 , C 3 -C 8 cycloalkyl groups, C 1 -C 6 alkylhydroxy groups, C 1 -C 6 alkylalkoxy groups, benzyl groups, and C 3 -C 8 heterocyclyl groups;

wherein at least one of R 6 and R 7 is hydrogen;

wherein R 1 and R 9 cannot both be absent; and

L is a linker.

2 . The compound or pharmaceutically acceptable salt of claim 1 , wherein the compound is:

3 . The compound or pharmaceutically acceptable salt of claim 1 , wherein the compound is:

4 . The compound or pharmaceutically acceptable salt of claim 1 , wherein the linker L comprises a cleavable peptide moiety.

5 . The compound or pharmaceutically acceptable salt of claim 4 , wherein the cleavable peptide moiety comprises valine-citrulline (Val-Cit), valine-alanine (Val-Ala), glutamic acid-valine-citrulline (Glu-Val-Cit), or alanine-alanine-asparagine (Ala-Ala-Asn).

6 . The compound or pharmaceutically acceptable salt of claim 4 , wherein the linker L comprises at least one spacer unit comprising: (i) a polyethylene glycol moiety, (ii) an alkyl moiety, or (iii) a combination of (i) and (ii).

7 . The compound or pharmaceutically acceptable salt of claim 4 , wherein the linker L comprises a maleimide (Mal) moiety.

8 . The compound or pharmaceutically acceptable salt of claim 4 , wherein the linker L comprises maleimidocaproyl (MC).

9 . The compound or pharmaceutically acceptable salt of claim 4 , wherein the linker L comprises p-aminobenzyl (pAB) or p-aminobenzyloxycarbonyl (pABC).

10 . The compound or pharmaceutically acceptable salt of claim 4 , wherein the linker L comprises MC-Val-Cit-pAB, MC-Val-Ala-pAB, MC-Glu-Val-Cit-pAB, MC-Ala-Ala-Asn-pAB, MC-Val-Cit-pABC, MC-Val-Ala-pABC, MC-Glu-Val-Cit-pABC, or MC-Ala-Ala-Asn-pABC.

11 . The compound or pharmaceutically acceptable salt of claim 1 , wherein the linker L comprises a cleavable glucuronide moiety.

12 . The compound or pharmaceutically acceptable salt of claim 11 , wherein the cleavable glucuronide moiety is cleavable by a glucuronidase.

13 . The compound or pharmaceutically acceptable salt of claim 11 , wherein the linker L comprises MC-β-glucuronide-pAB or MC-β-glucuronide-pABC.

14 . The compound or pharmaceutically acceptable salt of claim 1 , wherein the linker L is a non-cleavable linker comprising at least one spacer unit.

15 . The compound or pharmaceutically acceptable salt of claim 14 , wherein the linker L comprises a maleimide moiety.

16 . The compound or pharmaceutically acceptable salt of claim 15 , wherein the at least one spacer unit comprises (i) a polyethylene glycol moiety, (ii) an alkyl moiety, or (iii) a combination of (i) and (ii).

17 . The compound or pharmaceutically acceptable salt of claim 16 , wherein the linker L is chosen from:

and

18 . An antibody-drug conjugate of Formula (I):

Ab-(L-D) p   (I)

wherein:

Ab is an antibody or antigen binding fragment which targets a neoplastic cell;

L-D is a compound or pharmaceutically acceptable salt of claim 1 ; and

p is an integer from 1 to 15.

19 . The antibody-drug conjugate of claim 18 , wherein L-D is a compound of formula:

or a pharmaceutically acceptable salt thereof.

20 . The antibody-drug conjugate of claim 18 , wherein L-D is a compound of formula:

or a pharmaceutically acceptable salt thereof.

21 . The antibody-drug conjugate of claim 18 , wherein the linker L comprises a cleavable peptide moiety.

22 . The antibody-drug conjugate of claim 21 , wherein the cleavable peptide moiety comprises valine-citrulline (Val-Cit), valine-alanine (Val-Ala), glutamic acid-valine-citrulline (Glu-Val-Cit), or alanine-alanine-asparagine (Ala-Ala-Asn).

23 . The antibody-drug conjugate of claim 21 , wherein the linker L comprises at least one spacer unit comprising: (i) a polyethylene glycol moiety, (ii) an alkyl moiety, or (iii) a combination of (i) and (ii).

24 . The antibody-drug conjugate of claim 21 , wherein the linker L comprises a maleimide (Mal) moiety.

25 . The antibody-drug conjugate of claim 21 , wherein the linker L comprises maleimidocaproyl (MC).

26 . The antibody-drug conjugate of claim 21 , wherein the linker L comprises p-aminobenzyl (pAB) or p-aminobenzyloxycarbonyl (pABC).

27 . The antibody-drug conjugate of claim 21 , wherein the linker L comprises MC-Val-Cit-pAB, MC-Val-Ala-pAB, MC-Glu-Val-Cit-pAB, MC-Ala-Ala-Asn-pAB, MC-Val-Cit-pABC, MC-Val-Ala-pABC, MC-Glu-Val-Cit-pABC, or MC-Ala-Ala-Asn-pABC.

28 . The antibody-drug conjugate of claim 18 , wherein the linker L comprises a cleavable glucuronide moiety.

29 . The antibody-drug conjugate of claim 28 , wherein the linker L comprises MC-β-glucuronide-pAB or MC-β-glucuronide-pABC.

30 . The antibody-drug conjugate of claim 21 , wherein p is an integer from 2 to 8.

31 . A pharmaceutical composition comprising the antibody-drug conjugate of claim 18 and a pharmaceutical acceptable carrier.

32 . A method of treating a subject having, or suspected of having, a neoplastic disorder, comprising administering a therapeutically effective amount of the antibody-drug conjugate of claim 18 .

33 . The method of claim 32 , wherein the neoplastic disorder is a leukemia, a lymphoma, or a myeloma.

34 . The method of claim 33 , wherein the myeloma is multiple myeloma.

35 . A method of reducing or inhibiting growth of a tumor in a subject having, or suspected of having, a neoplastic disorder, comprising administering to the subject a therapeutically effective amount of the antibody-drug conjugate of claim 18 .

Assignments (4)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 14, 2025
From: BUONAMICI, SILVIA
To: EISAI R&D MANAGEMENT CO., LTD.
Reel/Frame 069851/0211 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 14, 2025
From: BUONAMICI, SILVIA
To: EISAI R&D MANAGEMENT CO., LTD.
Reel/Frame 069851/0218 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 14, 2025
From: BUONAMICI, SILVIA
To: EISAI R&D MANAGEMENT CO., LTD.
Reel/Frame 069851/0247 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 14, 2025
From: PAZOLLI, ERMIRA; SAMARAKOON, THIWANKA; PRAJAPATI, SUDEEP; FISHKIN, NATHAN; PALACINO, JAMES; SEILER, MICHAEL; ZHU, PING; COOK, ANDREW; SMITH, PETER; LIU, XIANG; ELLERY, SHELBY; REYNOLDS, DOMINIC; YU, LIHUA; CALANDRA, NICHOLAS; SHEEHAN, MEGAN; WU, ZHENHUA; PENG, SHOUYONG; XIAO, YONGHONG
To: EISAI R&D MANAGEMENT CO., LTD.
Reel/Frame 069892/0280 →
Continuity (7)
Continuation 17661909 · May 3, 2022
Continuation 17247117 · Nov 30, 2020
Continuation PCTUS2019035015 · May 31, 2019
Provisional Application 62779324 · Dec 13, 2018
Provisional Application 62679672 · Jun 1, 2018
Provisional Application 62679631 · Jun 1, 2018
Related Publication 20240360108A1 · Oct 31, 2024
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