IP Library Granted Patent US 10,647,764
Granted Patent B2
US 10,647,764 · App. 16/443,225 · Granted May 12, 2020

Agents, uses and methods for the treatment of synucleinopathy

Inventors: Pekka Kallunki (Valby, DK); Karina Fog (Valby, DK); Louise Buur Vesterager (Valby, DK); Ann-Louise Bergstrôm (Valby, DK); Florence Sotty (Valby, DK); David Satijn (Utrecht, NL); Edward Van Den Brink (Utrecht, DK); Paul Parren (Utrecht, NL); Rik Rademaker (Utrecht, NL); Tom Vink (Utrecht, NL); Ibrahim John Malik (Valby, DK); Liliana Christina Pereira Montezinho (Valby, DK)
Assignee: H. Lundbeck A/S
C07K16/18A61K39/3955A61K51/00A61P25/16A61P25/28G01N33/6896A61K2039/505C07K2317/21C07K2317/33C07K2317/34C07K2317/56C07K2317/565C07K2317/76C07K2317/92G01N2800/2835
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 10,647,764
App. No.
16/443,225
Granted
May 12, 2020
Kind
B2
Abstract

The invention relates to novel monoclonal anti-alpha-synuclein antibodies. The antibodies can be used for treating a synucleinopathy such as Parkinson's disease (including idiopathic and inherited forms of Parkinson's disease), Diffuse Lewy Body Disease (DLBD), Lewy body variant of Alzheimer's disease (LBV), Combined Alzheimer's and Parkinson disease, pure autonomic failure and multiple system atrophy.

Claims (14)

1. A method of treating Parkinson's disease or other synucleinopathy in a human subject in need thereof, the method comprising administering to the subject a therapeutically effective amount of an antibody which specifically binds to human alpha-synuclein and comprises heavy chain CDR1, CDR2, and CDR3 comprising the amino acid sequences of SEQ ID NOs: 1, 34, and 3, respectively, and light chain CDR1, CDR2, and CDR3 comprising the amino acid sequences of SEQ ID NOs: 4, 5, and 6, respectively.

2. The method of claim 1 , wherein the Parkinson's disease is an idiopathic or inherited form of Parkinson's disease.

3. The method of claim 1 , wherein the synucleinopathy is selected from Gaucher's Disease, Diffuse Lew Body Disease, Lewy body variant of Alzheimer's disease, combined Alzheimer's and Parkinson's disease, pure autonomic failure, and multiple system atrophy.

4. The method of claim 1 , wherein the antibody is which is a single chain Fv, a disulphide-bonded Fv, an Fab fragment, a Fab′ fragment, or a F(ab) 2 fragment.

5. The method of claim 1 , wherein the antibody is a human antibody.

6. The method of claim 1 , wherein the antibody comprises a heavy chain variable domain comprising the amino acid sequence of SEQ ID NO:31 and a light chain variable domain comprising the amino acid sequence of SEQ ID NO:8.

7. The method of claim 1 , wherein the antibody binds an epitope within amino acid residues 112-117 (SEQ ID NO:9) of human alpha-synuclein (SEQ ID NO:10).

8. The method of claim 1 , wherein the antibody is formulated in a pharmaceutical composition.

9. A method of treating Parkinson's disease in a human subject in need thereof, the method comprising administering to the subject a therapeutically effective amount of an antibody which specifically binds to human alpha-synuclein and comprises heavy chain CDR1, CDR2, and CDR3 comprising the amino acid sequences of SEQ ID NOs: 1, 34, and 3, respectively, and light chain CDR1, CDR2, and CDR3 comprising the amino acid sequences of SEQ ID NOs: 4, 5, and 6, respectively.

10. The method of claim 9 , wherein the antibody is which is a single chain Fv, a disulphide-bonded Fv, an Fab fragment, a Fab′ fragment, or a F(ab) 2 fragment.

11. The method of claim 9 , wherein the antibody is a human antibody.

12. The method of claim 9 , wherein the antibody comprises a heavy chain variable domain comprising the amino acid sequence of SEQ ID NO:31 and a light chain variable domain comprising the amino acid sequence of SEQ ID NO:8.

13. The method of claim 9 , wherein the antibody binds an epitope within amino acid residues 112-117 (SEQ ID NO:9) of human alpha-synuclein (SEQ ID NO:10).

14. The method of claim 9 , wherein the antibody is formulated in a pharmaceutical composition.

Assignments (4)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 21, 2023
From: STAVENHAGEN, JEFFREY B
To: H. LUNDBECK A/S
Reel/Frame 064340/0504 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 19, 2019
From: KALLUNKI, PEKKA; FOG, KARINA; VESTERAGER, LOUISE BUUR; BERGSTROM, ANN-LOUISE; SOTTY, FLORENCE; MALIK, IBRAHIM JOHN; MONTEZINHO, LILIANA CHRISTINA PEREIRA
To: H. LUNDBECK A/S
Reel/Frame 049517/0331 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 19, 2019
From: VAN DEN BRINK, EDWARD; PARREN, PAUL; RADEMAKER, RIK; SATIJN, DAVID; VINK, TOM
To: GENMAB A/S
Reel/Frame 049517/0389 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 19, 2019
From: GENMAB A/S
To: H. LUNDBECK A/S
Reel/Frame 049517/0467 →
Priority Claims (1)
GB 1512203.9 · Jul 13, 2015 · national
Continuity (2)
Division 15207859 · Jul 12, 2016
Related Publication 20190382473A1 · Dec 19, 2019
Cited By (4)
US 12,351,624 US 12,358,974 US 12,358,975 US 12,421,303