IP Library › Granted Patent US 11,584,799
Granted Patent B2
US 11,584,799 · App. 16/580,483 · Granted Feb 21, 2023

Anti-CD30 antibodies and methods for treating CD30+ cancer

Inventors: Jeffrey A. Medin (Shorewood, WI); Mary L. Faber (New Berlin, WI); Everett R. Tate (Greendale, WI); Robyn A. A. Oldham (Milwaukee, WI)
Assignees: Medical College of Wisconsin, Inc.; University of Virginia Patent Foundation
C07K16/2878A61K39/3955A61K47/6849A61P35/00A61P35/02C07K14/7051C07K16/462C07K19/00C07K14/70578C07K2317/24C07K2317/41C07K2317/51C07K2317/54C07K2317/55C07K2317/565C07K2317/622C07K2317/76C07K2319/02C07K2319/03C07K2319/30C07K2319/33
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Quick Facts
Patent No.
US 11,584,799
App. No.
16/580,483
Granted
Feb 21, 2023
Kind
B2
Abstract

The present invention provides novel antibodies and antigen binding fragments thereof that bind to human CD30. Also presented are single chain variable antibodies, chimeric antigen receptors and uses thereof. Methods of treating cancer are also disclosed.

Claims (42)

1. An isolated antibody or antigen-binding fragment thereof capable of binding human CD30 comprising a single light chain variable region and a single heavy chain variable region comprising:

(a) a light chain variable domain comprising a CDRL1 region of SEQ ID NO:2, a CDRL2 region of SEQ ID NO:3, and a CDRL3 region of SEQ ID NO:4 and a heavy chain variable domain comprising a CDRH1 region of SEQ ID NO:6, a CDRH2 region of SEQ ID NO:7, and a CDRH3 region of SEQ ID NO:8;

(b) a light chain variable domain comprising a CDRL1 region of SEQ ID NO:10, a CDRL2 region of SEQ ID NO:11, and a CDRL3 region of SEQ ID NO:12 and a heavy chain variable domain comprising a CDRH1 region of SEQ ID NO:14, a CDRH2 region of SEQ ID NO:15, and a CDRH3 region of SEQ ID NO:16;

(c) a light chain variable domain comprising a CDRL1 region of SEQ ID NO:18, a CDRL2 region of SEQ ID NO:19, and a CDRL3 region of SEQ ID NO:20 and a heavy chain variable domain comprising a CDRH1 region of SEQ ID NO:22, a CDRH2 region of SEQ ID NO:23, and a CDRH3 region of SEQ ID NO:24;

(d) a light chain variable domain comprising a CDRL1 region of SEQ ID NO:26, a CDRL2 region of SEQ ID NO:27, and a CDRL3 region of SEQ ID NO:28 and a heavy chain variable domain comprising a CDRH1 region of SEQ ID NO:30, a CDRH2 region of SEQ ID NO:31, and a CDRH3 region of SEQ ID NO:32; or

(e) a light chain variable domain comprising a CDRL1 region of SEQ ID NO:34, a CDRL2 region of SEQ ID NO:35, and a CDRL3 region of SEQ ID NO:36 and a heavy chain variable domain comprising a CDRH1 region of SEQ ID NO:38, a CDRH2 region of SEQ ID NO:39, and a CDRH3 region of SEQ ID NO:40.

2. The isolated antibody or antigen-binding fragment thereof of claim 1 , wherein the antibody or antigen-binding fragment thereof comprises a heavy and a light chain selected from the group consisting of:

(a) a light chain comprising SEQ ID NO:1 or a sequence with at least 85% similarity to SEQ ID NO:1, and a heavy chain comprising SEQ ID NO:5 or a sequence with at least 85% similarity to SEQ ID NO:5;

(b) a light chain comprising SEQ ID NO:9 or a sequence with at least 85% similarity to SEQ ID NO:9, and a heavy chain comprising SEQ ID NO:13 or a sequence with at least 85% similarity to SEQ ID NO:13;

(c) a light chain comprising SEQ ID NO:17 or a sequence with at least 85% similarity to SEQ ID NO:17, and a heavy chain comprising SEQ ID NO:21 or a sequence with at least 85% similarity to SEQ ID NO:21;

(d) a light chain comprising SEQ ID NO:25 or a sequence with at least 85% similarity to SEQ ID NO:25, and a heavy chain comprising SEQ ID NO:29 or a sequence with at least 85% similarity to SEQ ID NO:29; and

(e) a light chain comprising SEQ ID NO:33 or a sequence with at least 85% similarity to SEQ ID NO:33, and a heavy chain comprising SEQ ID NO:37 or a sequence with at least 85% similarity to SEQ ID NO:37.

3. The isolated antibody or antigen-binding fragment thereof of claim 1 , wherein the antibody is selected from the group consisting of a monoclonal antibody, a humanized antibody, a single chain variable fragment (scFv) antibody, a single domain antibody, and a chimeric antibody.

4. The isolated antibody or antigen-binding fragment thereof of claim 1 , wherein the antibody is a monoclonal antibody.

5. The isolated antibody of claim 4 , wherein the antibody is a mouse, humanized or chimeric antibody.

6. The isolated antibody or antigen-binding fragment thereof of claim 1 , wherein the antibody is a humanized antibody.

7. The isolated antibody or antigen-binding fragment thereof of claim 1 , wherein the antibody or antigen-binding fragment thereof is engrafted within a full IgG scaffold or a scFv scaffold.

8. The isolated antibody or antigen-binding fragment thereof of claim 7 , wherein the scaffold is human in origin.

9. The isolated antibody or antigen-binding fragment of claim 1 , wherein the antigen-binding fragment thereof is a single chain variable fragment (scFv), and wherein the light chain and heavy chain are linked via a linker amino acid sequence.

10. The isolated antibody or antigen-binding fragment of claim 9 , wherein the single chain variable fragment comprises an amino acid sequence selected from the group consisting of SEQ ID NO:42, 44, 46, 48, 50, and 52.

11. A composition comprising the isolated antibody of claim 1 and a pharmaceutically acceptable carrier.

12. A method of treating a patient having a CD30+ cancer, the method comprising

(a) administering a therapeutically effective amount of the isolated antibody or antigen-binding fragment thereof capable of binding human CD30 of claim 1 .

13. The method of claim 12 , wherein the CD30+ cancer is Hodgkin's lymphoma or acute myeloid leukemia (AML).

14. The method of claim 12 , wherein the antibody is directly or indirectly conjugated to a therapeutic agent.

15. The method of claim 14 , wherein the therapeutic agent is a chemotherapy agent.

16. A method of inhibiting growth of a tumor cell expressing CD30, comprising contacting the tumor cell with an effective amount of the antibody or antigen-binding fragment thereof of claim 1 such that the growth of the cell is inhibited.

17. A chimeric antigen receptor (CAR) comprising a CD30 binding domain, a hinge region, a transmembrane domain, a costimulatory domain, and an intracellular signaling domain,

wherein the intracellular signaling domain comprises a CD3 ζ-chain, and

wherein the CD30 binding domain comprises:

(a) a light chain variable domain comprising a CDRL1 region of SEQ ID NO:2, a CDRL2 region of SEQ ID NO:3, and a CDRL3 region of SEQ ID NO:4 and a heavy chain variable domain comprising a CDRH1 region of SEQ ID NO:6, a CDRH2 region of SEQ ID NO:7, and a CDRH3 region of SEQ ID NO:8;

(b) a light chain variable domain comprising a CDRL1 region of SEQ ID NO:10, a CDRL2 region of SEQ ID NO:11, and a CDRL3 region of SEQ ID NO:12 and a heavy chain variable domain comprising a CDRH1 region of SEQ ID NO:14, a CDRH2 region of SEQ ID NO:15, and a CDRH3 region of SEQ ID NO:16;

(c) a light chain variable domain comprising a CDRL1 region of SEQ ID NO:18, a CDRL2 region of SEQ ID NO:19, and a CDRL3 region of SEQ ID NO:20 and a heavy chain variable domain comprising a CDRH1 region of SEQ ID NO:22, a CDRH2 region of SEQ ID NO:23, and a CDRH3 region of SEQ ID NO:24;

(d) a light chain variable domain comprising a CDRL1 region of SEQ ID NO:26, a CDRL2 region of SEQ ID NO:27, and a CDRL3 region of SEQ ID NO:28 and a heavy chain variable domain comprising a CDRH1 region of SEQ ID NO:30, a CDRH2 region of SEQ ID NO:31, and a CDRH3 region of SEQ ID NO:32; or

(e) a light chain variable domain comprising a CDRL1 region of SEQ ID NO:34, a CDRL2 region of SEQ ID NO:35, and a CDRL3 region of SEQ ID NO:36 and a heavy chain variable domain comprising a CDRH1 region of SEQ ID NO:38, a CDRH2 region of SEQ ID NO:39, and a CDRH3 region of SEQ ID NO:40.

18. The CAR of claim 17 , wherein the CD30 binding domain comprises a heavy and a light chain selected from the group consisting of:

(a) a light chain comprising SEQ ID NO:1 or a sequence with at least 85% similarity to SEQ ID NO:1, and a heavy chain comprising SEQ ID NO:5 or a sequence with at least 85% similarity to SEQ ID NO:5;

(b) a light chain comprising SEQ ID NO:9 or a sequence with at least 85% similarity to SEQ ID NO:9, and a heavy chain comprising SEQ ID NO:13 or a sequence with at least 85% similarity to SEQ ID NO:13;

(c) a light chain comprising SEQ ID NO:17 or a sequence with at least 85% similarity to SEQ ID NO:17, and a heavy chain comprising SEQ ID NO:21 or a sequence with at least 85% similarity to SEQ ID NO:21;

(d) a light chain comprising SEQ ID NO:25 or a sequence with at least 85% similarity to SEQ ID NO:25, and a heavy chain comprising SEQ ID NO:29 or a sequence with at least 85% similarity to SEQ ID NO:29; and

(e) a light chain comprising SEQ ID NO:33 or a sequence with at least 85% similarity to SEQ ID NO:33, and a heavy chain comprising SEQ ID NO:37 or a sequence with at least 85% similarity to SEQ ID NO:37.

19. The CAR of claim 17 , wherein the CD30 binding domain comprises a single chain variable fragment (scFv), wherein the light chain and heavy chain are linked via a linker amino acid sequence, and wherein the scFv comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 42, 44, 46, 48, 50, and 52.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 6, 2022
From: MEDICAL COLLEGE OF WISCONSIN, INC.
To: UNIVERSITY OF VIRGINIA PATENT FOUNDATION D/B/A THE UNIVERSITY OF VIRGINIA LICENSING & VENTURES GROUP
Reel/Frame 060996/0321 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 28, 2020
From: MEDIN, JEFFREY A.; FABER, MARY L.; TATE, EVERETT R.; OLDHAM, ROBYN A.A.
To: MEDICAL COLLEGE OF WISCONSIN, INC.
Reel/Frame 053328/0547 →
Continuity (2)
Provisional Application 62735508 · Sep 24, 2018
Related Publication 20200095329A1 · Mar 26, 2020
Cited By (2)
US 12,351,639 US 12,391,764