IP Library Granted Patent US 11,857,637
Granted Patent B2
US 11,857,637 · App. 17/519,183 · Granted Jan 2, 2024

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

Inventors: David Rabuka (Kensington, CA); Penelope M. Drake (Castro Valley, CA)
Assignee: R.P. Scherer Technologies, LLC
A61K47/6807C07K16/2866A61K47/65
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Quick Facts
Patent No.
US 11,857,637
App. No.
17/519,183
Granted
Jan 2, 2024
Kind
B2
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.

Claims (58)

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.

Assignments (2)
SECURITY INTEREST Recorded Dec 19, 2024
From: CATALENT CTS (KANSAS CITY), LLC; REDWOOD BIOSCIENCE, INC.; R.P. SCHERER TECHNOLOGIES, LLC; CATALENT WELLNESS, LLC; CATALENT PHARMA SOLUTIONS, INC.; CATALENT WELLNESS NEW JERSEY, LLC; CATALENT MARYLAND, INC.; CATALENT GREENVILLE, INC.; CATALENT MICRON TECHNOLOGIES, INC.; CATALENT SAN DIEGO, INC.; CATALENT WELLNESS VIRGINIA, LLC; CATALENT USA PACKAGING, LLC; CATALENT PHARMA SOLUTIONS, LLC
To: ARES CAPITAL CORPORATION, AS COLLATERAL AGENT
Reel/Frame 069743/0458 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 17, 2021
From: RABUKA, DAVID; DRAKE, PENELOPE M.
To: R.P. SCHERER TECHNOLOGIES, LLC
Reel/Frame 058418/0578 →