IP Library › Granted Patent US 11,673,943
Granted Patent B2
US 11,673,943 · App. 17/104,848 · Granted Jun 13, 2023

Methods of binding amyloid beta protein having pyroglutamate at the third amino acid residue (3pE abeta) in vivo using anti-3pE abeta antibodies or antigen-binding fragments thereof

Inventors: Marc Mercken (Turnhout, BE); Bianca Van Broeck (Schilde, BE); Marc Vandermeeren (Geel, BE); Bart Hermans (Beerse, BE); Astrid Bottelbergs (Antwerp, BE)
Assignee: Janssen Pharmaceutica NV
C07K16/18A61K39/3955A61P25/28C07K14/4711G01N33/6896A01K2267/0312A61K39/395A61K49/00A61K2039/505C07K2317/24C07K2317/33C07K2317/34C07K2317/51C07K2317/515C07K2317/55C07K2317/56C07K2317/565C07K2317/567C07K2317/76C07K2317/92C12Q1/37G01N33/533G01N2333/4709G01N2333/96425G01N2800/2814G01N2800/2821
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Quick Facts
Patent No.
US 11,673,943
App. No.
17/104,848
Granted
Jun 13, 2023
Kind
B2
Abstract

The invention provides an antibody or antigen binding fragments thereof that binds to 3pE Aβ and methods of making and using the antibody or antigen binding fragment thereof, including use for formulations, administration and kits. The antibody and antigen binding fragments thereof and methods disclosed are useful for diagnosis, prognosis and treatment of Alzheimer's disease or other β-amyloid-related diseases.

Claims (45)

1. A method of binding amyloid β protein having pyroglutamate at the third amino acid residue (3pE Aβ) in a subject, the method comprising administering to the subject an antibody or antigen binding fragment comprising:

(a) a heavy chain variable region CDR1 comprising the amino acid sequence of SEQ ID NO:3,

(b) a heavy chain variable region CDR2 comprising the amino acid sequence of SEQ ID NO:4,

(c) a heavy chain variable region CDR3 comprising the amino acid sequence of SEQ ID NO:5,

(d) a light chain variable region CDR1 comprising the amino acid sequence of SEQ ID NO:14,

(e) a light chain variable region CDR2 comprising the amino acid sequence of SEQ ID NO:15, and

(f) a light chain variable region CDR3 comprising the amino acid sequence of SEQ ID NO:16.

2. The method of claim 1 wherein:

(a) the heavy chain variable region CDR1 consists of the amino acid sequence of SEQ ID NO:3,

(b) the heavy chain variable region CDR2 consists of the amino acid sequence of SEQ ID NO:4,

(c) the heavy chain variable region CDR3 consists of the amino acid sequence of SEQ ID NO:5,

(d) the light chain variable region CDR1 consists of the amino acid sequence of SEQ ID NO:14,

(e) the light chain variable region CDR2 consists of the amino acid sequence of SEQ ID NO:15, and

(f) the light chain variable region CDR3 consists of the amino acid sequence of SEQ ID NO:16.

3. The method of claim 1 , wherein the antibody or antigen binding fragment thereof comprises (a) a heavy chain variable region comprising the amino acid sequence of SEQ ID NO:2; and (b) a light chain variable region comprising the amino acid sequence of SEQ ID NO:13.

4. The method of claim 1 , wherein the antibody or antigen binding fragment thereof comprises (a) a heavy chain comprising the amino acid sequence of SEQ ID NO: 1; and (b) a light chain comprising the amino acid sequence of SEQ ID NO: 12.

5. The method of claim 1 , wherein the antibody or antigen binding fragment thereof comprises (a) a heavy chain variable region comprising an amino acid sequence at least 98% identical to the amino acid sequence of SEQ ID NO:2; and (b) a light chain variable region of comprising an amino acid sequence at least 98% identical to the amino acid sequence of SEQ ID NO:13.

6. The method of claim 2 , wherein the antibody or antigen binding fragment thereof comprises (a) a heavy chain variable region of comprising an amino acid sequence at least 98% identical to the amino acid sequence of SEQ ID NO:2; and (b) a light chain variable region of comprising an amino acid sequence that is at least 98% identical to the amino acid sequence of SEQ ID NO:13.

7. The method of claim 1 , wherein the antibody or antigen binding fragment thereof is humanized.

8. The method of claim 2 , wherein the antibody or antigen binding fragment thereof is humanized.

9. The method of claim 1 , wherein the antibody or antigen binding fragment thereof is formulated in a pharmaceutical composition comprising a pharmaceutically acceptable carrier.

10. The method of claim 1 , wherein the 3pE Aβ is in an amyloid plaque deposit.

11. The method of claim 1 , wherein the subject has Alzheimer's disease.

12. A method of binding amyloid plaque comprising amyloid β protein having pyroglutamate at the third amino acid residue (3pE Aβ) in a subject, the method comprising administering to the subject an antibody or antigen binding fragment comprising:

(a) a heavy chain variable region CDR1 comprising the amino acid sequence of SEQ ID NO:3,

(b) a heavy chain variable region CDR2 comprising the amino acid sequence of SEQ ID NO:4,

(c) a heavy chain variable region CDR3 comprising the amino acid sequence of SEQ ID NO:5,

(d) a light chain variable region CDR1 comprising the amino acid sequence of SEQ ID NO:14,

(e) a light chain variable region CDR2 comprising the amino acid sequence of SEQ ID NO:15, and

(f) a light chain variable region CDR3 comprising the amino acid sequence of SEQ ID NO:16.

13. The method of claim 12 , wherein:

(a) the heavy chain variable region CDR1 consists of the amino acid sequence of SEQ ID NO:3,

(b) the heavy chain variable region CDR2 consists of the amino acid sequence of SEQ ID NO:4,

(c) the heavy chain variable region CDR3 consists of the amino acid sequence of SEQ ID NO:5,

(d) the light chain variable region CDR1 consists of the amino acid sequence of SEQ ID NO:14,

(e) the light chain variable region CDR2 consists of the amino acid sequence of SEQ ID NO:15, and

(f) the light chain variable region CDR3 consists of the amino acid sequence of SEQ ID NO:16.

14. The method of claim 12 , wherein the antibody or antigen binding fragment thereof comprises (a) a heavy chain variable region comprising the amino acid sequence of SEQ ID NO:2; and (b) a light chain variable region comprising the amino acid sequence of SEQ ID NO:13.

15. The method of claim 12 , wherein the antibody or antigen binding fragment thereof comprises (a) a heavy chain comprising the amino acid sequence consisting of SEQ ID NO: 1; and (b) a light chain of comprising the amino acid sequence consisting of SEQ ID NO: 12.

16. The method of claim 12 , wherein the antibody or antigen binding fragment thereof comprises (a) a heavy chain variable region comprising an amino acid sequence at least 98% identical to the amino acid sequence of SEQ ID NO:2; and (b) a light chain variable region of comprising an amino acid sequence at least 98% identical to the amino acid sequence of SEQ ID NO:13.

17. The method of claim 13 , wherein the antibody or antigen binding fragment thereof comprises (a) a heavy chain variable region of comprising an amino acid sequence at least 98% identical to the amino acid sequence of SEQ ID NO:2; and (b) a light chain variable region of comprising an amino acid sequence that is at least 98% identical to the amino acid sequence of SEQ ID NO:13.

18. The method of claim 12 , wherein the antibody or antigen binding fragment thereof is humanized.

19. The method of claim 13 , wherein the antibody or antigen binding fragment thereof is humanized.

20. The method of claim 12 , wherein the antibody or antigen binding fragment thereof is formulated in a pharmaceutical composition comprising a pharmaceutically acceptable carrier.

21. The method of claim 12 , wherein the subject has Alzheimer's disease.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 8, 2021
From: MERCKEN, MARC; VAN BROECK, BIANCA; VANDERMEEREN, MARC; HERMANS, BART; BOTTELBERGS, ASTRID
To: JANSSEN PHARMACEUTICA NV
Reel/Frame 055524/0609 →
Continuity (4)
Continuation 16688406 · Nov 19, 2019
Division 15801435 · Nov 2, 2017
Provisional Application 62416788 · Nov 3, 2016
Related Publication 20210147528A1 · May 20, 2021