IP Library Granted Patent US 9,309,309
Granted Patent B2
US 9,309,309 · App. 14/326,974 · Granted Apr 12, 2016

Anti-ADDL monoclonal antibody and uses thereof

Inventors: Renee C. Gaspar (Souderton, PA); Paul J. Shughrue (West Chester, PA); Fubao Wang (Dresher, PA); Weirong Wang (Harleysville, PA); Ningyan Zhang (Ambler, PA); Wei-Qin Zhao (North Wales, PA); Min Xu (Ambler, PA); Alexander McCampbell (Chalfont, PA)
Assignee: Merck Sharp & Dohme Corp.
C07K16/18A61K39/3955A61K45/06A61K2039/505C07K2317/24C07K2317/55C07K2317/565C07K2317/64C07K2317/76C07K2317/90C07K2317/92C07K2317/94
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Quick Facts
Patent No.
US 9,309,309
App. No.
14/326,974
Granted
Apr 12, 2016
Kind
B2
Abstract

The present invention relates to antibodies that bind amyloid β-derived diffusible ligands, also known as ADDLs. The antibodies of the invention are selective for ADDLs, can penetrate the brain, and are useful in methods of detecting ADDLs and diagnosing Alzheimer's disease. The present antibodies also block binding of ADDLs to neurons, assembly of ADDLS, and tau phosphorylation and are there useful in methods for the preventing and treating diseases associated with ADDLs.

Claims (18)

1. An isolated antibody, or an antigen binding fragment thereof, that binds amyloid β-derived diffusible ligands, said antibody or fragment comprising:

(a) a light chain variable region comprising,

(i) a CDR1 of SEQ ID NO:1,

(ii) a CDR2 of SEQ ID NO:2,

(iii) a CDR3 of SEQ ID NO:10; and

(b) a heavy chain variable region comprising,

(i) a CDR1 of SEQ ID NO:4,

(ii) a CDR2 of SEQ ID NO:5, and

(iii) a CDR3 of SEQ ID NO:6.

2. The isolated antibody of claim 1 wherein the light chain variable region of said antibody comprises SEQ ID NO:15 and the heavy chain variable region of said antibody comprises SEQ ID NO:17.

3. The isolated antibody of claim 1 further comprising a heavy chain constant region of SEQ ID NO:21.

4. The isolated antibody of claim 1 , wherein the antibody is a monoclonal antibody.

5. A pharmaceutical composition comprising the antibody or antigen binding fragment of claim 1 in admixture with a pharmaceutically acceptable carrier.

6. A method for attenuating binding of amyloid β-derived diffusible ligands to a neuron comprising contacting the neuron with the antibody or antigen binding fragment of claim 1 so that binding of Aβ-derived diffusible ligands to the neuron is attenuated.

7. A method for inhibiting assembly of amyloid β-derived diffusible ligands comprising contacting a sample containing amyloid β 1-42 peptides with the antibody or antigen binding fragment of claim 1 thereby inhibiting assembly of Aβ-derived diffusible ligands.

8. A method for inhibiting the phosphorylation of tau protein at Ser202/Thr205 comprising contacting a sample containing a tau protein with the antibody or antigen binding fragment of claim 1 thereby inhibiting the phosphorylation of tau protein at Ser202/Thr205.

9. A method for attenuating the symptoms of a disease associated with amyloid β-derived diffusible ligands comprising administering an effective amount of the pharmaceutical composition of claim 5 .

10. A kit for detecting amyloid β-derived diffusible ligands comprising the antibody or antigen binding fragment of claim 1 .

Assignments (2)
CHANGE OF NAME Recorded Jun 20, 2023
From: MERCK SHARP & DOHME CORP.
To: MERCK SHARP & DOHME LLC
Reel/Frame 063996/0418 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 12, 2016
From: GASPAR, RENEE C.; SHUGHRUE, PAUL J.; WANG, FUBAO; WANG, WEIRONG; ZHANG, NINGYAN; ZHAO, WEI-QIN; XU, MIN; MCCAMPBELL, ALEXANDER
To: MERCK SHARP & DOHME CORP.
Reel/Frame 037727/0069 →
Continuity (3)
Continuation 13809475
Provisional Application 61364210 · Jul 14, 2010
Related Publication 20150023952A1 · Jan 22, 2015