Anti-CD25 antibody-maytansine conjugates and methods of use thereof

Patent metadata

Field	Value
Publication number	US-11857637-B2
Application number	US-202117519183-A
Country	US
Kind code	B2
Filing date	Nov 4, 2021
Priority date	Oct 4, 2019
Publication date	Jan 2, 2024
Grant date	Jan 2, 2024

Abstract

The present disclosure provides anti-CD25 antibody-maytansine conjugate structures. The disclosure also encompasses methods of production of such conjugates, as well as methods of using the same.

First claim

What is claimed is:

1. A conjugate of formula (I):

wherein
Z is CR 4 or N;
R 1 is selected from hydrogen, alkyl, substituted alkyl, alkenyl, substituted alkenyl, alkynyl, substituted alkynyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl, cycloalkyl, substituted cycloalkyl, heterocyclyl, and substituted heterocyclyl;
R 2 and R 3 are each independently selected from hydrogen, alkyl, substituted alkyl, alkenyl, substituted alkenyl, alkynyl, substituted alkynyl, alkoxy, substituted alkoxy, amino, substituted amino, carboxyl, carboxyl ester, acyl, acyloxy, acyl amino, amino acyl, alkylamide, substituted alkylamide, sulfonyl, thioalkoxy, substituted thioalkoxy, aryl, substituted aryl, heteroaryl, substituted heteroaryl, cycloalkyl, substituted cycloalkyl, heterocyclyl, and substituted heterocyclyl, or R 2 and R 3 are optionally cyclically linked to form a 5 or 6-membered heterocyclyl;
each R 4 is independently selected from hydrogen, halogen, alkyl, substituted alkyl, alkenyl, substituted alkenyl, alkynyl, substituted alkynyl, alkoxy, substituted alkoxy, amino, substituted amino, carboxyl, carboxyl ester, acyl, acyloxy, acyl amino, amino acyl, alkylamide, substituted alkylamide, sulfonyl, thioalkoxy, substituted thioalkoxy, aryl, substituted aryl, heteroaryl, substituted heteroaryl, cycloalkyl, substituted cycloalkyl, heterocyclyl, and substituted heterocyclyl;
L is a linker comprising (T 1 -V 1 ) a -(T 2 -V 2 ) b -(T 3 -V 3 ) c , wherein a, b, and c are 1;
T 1 , is selected from (C 1 -C 12 )alkyl and substituted (C 1 -C 12 )alkyl;
T 2 is 4-amino-piperidine (4AP) having the structure:

T 3 is selected from (C 1 -C 12 )alkyl and substituted (C 1 -C 12 )alkyl;
V 1 , V 2 , and V 3 are each —CO—;
each f is independently an integer from 0 to 12;
each n is independently an integer from 0 to 30;
W 1 is a maytansinoid;
W 2 is an anti-CD25 antibody comprising a heavy chain comprising complementarity determining regions (CDRs) of SYRMH (SEO ID NO: 6), YINPSTGYTEYNQKFKD (SEQ ID NO: 7) and GGGVFDY (SEQ ID NO: 8); and a light chain comprising the CDRs of SASSSISYMH (SEQ ID NO: 9), YTSILHS (SEQ ID NO: 10), and QQGNTLPWT (SEQ ID NO: 11);
and wherein the anti-CD25 antibody comprises at the C-terminus of the heavy chain constant region a sequence of formula (II):
X 1 (FGly′)X 2 Z 20 X 3 Z 30   (II)

wherein FGly′ is the amino acid residue coupled to the linker;
Z 20 is either a proline or alanine residue;
Z 30 is a basic amino acid or an aliphatic amino acid;
X may be present or absent and, when present, can be any amino acid;
X 2 and X 3 are each independently any amino acid.

2. The conjugate of claim 1 , wherein the maytansinoid is of the formula:

where indicates the point of attachment between the maytansinoid and L.

3. The conjugate of claim 1 , wherein
T 1 is (C 1 -C 12 )alkyl, and T 3 is (C 1 -C 12 )alkyl.

4. The conjugate of claim 1 ,
wherein each f is independently and integer from 1 to 12; and
N is an integer from 1 to 30.

5. The conjugate of claim 1 , wherein the anti-CD25 antibody is an IgG1 antibody.

6. The conjugate of claim 4 , wherein the anti-CD25 antibody is an IgG1 kappa antibody.

7. The conjugate of claim 1 , wherein the sequence of formula (II) is L(FGly′)TPSR (SEQ ID NO: 144).

8. The conjugate of claim 1 , wherein
Z30 is selected from R, K, H, A, G, L, V, I and P;
X1 is selected from L, M, S and V; and
X2 and X3 are each independently selected from S, T, A, V, G and C.

9. The conjugate of claim 1 , wherein
the formula (II) sequence is C-terminal to the amino acid sequence SLSLSPG (SEQ ID NO: 145).

10. The conjugate of claim 9 , wherein the heavy chain constant region comprises the sequence SPGSL(FGly′)TPSRGS (SEQ ID NO: 149).

11. The conjugate of claim 9 , wherein
Z 30 is selected from R, K, H, A, G, L, V, I, and P;
X 1 is selected from L, M, S, and V; and
X 2 and X 3 are each independently selected from S, T, A, V, G, and C.

12. The conjugate of claim 1 , wherein the anti-CD25 antibody is daclizumab.

13. A pharmaceutical composition comprising:
a conjugate of claim 1 ; and
a pharmaceutically-acceptable excipient.

14. A method of treating a subject for a hematological cancer, wherein the hematological cancer comprises cells expressing CD25, the method comprising:
administering to the subject a therapeutically effective amount of a pharmaceutical composition comprising a conjugate of claim 1 , wherein the administering is effective to treat the subject for the hematological cancer.

15. The method according to claim 14 , wherein the hematologic cancer is leukemia.

16. The method according to claim 15 , wherein the leukemia is acute myeloid leukemia (AML).

17. The method according to claim 16 , wherein the AML is refractory AML.

18. The method according to claim 14 , wherein the hematologic cancer is lymphoma.

19. The method according to claim 18 , wherein the lymphoma is Hodgkin lymphoma (HL).

20. The method according to claim 18 , wherein the lymphoma is Non-Hodgkin lymphoma (NHL).

21. The method of claim 14 , wherein the anti-CD25 antibody of the conjugate is daclizumab.

22. A method of reducing inhibitory signals derived from T regulatory cells in a subject, the method comprising:
administering to the subject a therapeutically effective amount of a pharmaceutical composition comprising a conjugate of claim 1 , wherein the administering is effective to reduce inhibitory signals derived from T regulatory cells in the subject.

Assignees

• Scherer Technologies Llc R P

Inventors

• Rabuka David
• Drake Penelope M

Classifications

• A61K47/68033

  the drug being a maytansine · CPC title

• A61K47/6807 Primary

  the drug or compound being a sugar, nucleoside, nucleotide, nucleic acid, e.g. RNA antisense · CPC title

• C07D471/04 Primary

  Ortho-condensed systems · CPC title

• C07K16/2866

  against receptors for cytokines, lymphokines, interferons · CPC title

• A61K47/65

  Peptidic linkers, binders or spacers, e.g. peptidic enzyme-labile linkers · CPC title