IP Library › Granted Patent US 10,537,573
Granted Patent B2
US 10,537,573 · App. 15/112,818 · Granted Jan 21, 2020

Combinations comprising positive allosteric modulators or orthosteric agonists of metabotropic glutamatergic receptor subtype 2 and their use

Inventors: Brian D. Klein (Potomac, MD); Hilde Lavreysen (Lommel, BE); Stefan Maria Christiaan Pype (Boechout, BE); Roy E. Twyman (Doylestown, PA); Nancy Eulalie Sylvain Van Osselaer (Lier, BE); H. Steven White (Seattle, WA); Marc André Ceusters (Diest, BE); José Maria Cid-Núñez (Toledo, ES); Andrés Avelino Trabanco-Suárez (Olias del Rey, ES); Roger Francis Bone (Bridgewater, NJ)
Assignee: Janssen Pharmaceutica NV
A61K31/506A61K31/381A61K31/4015A61K31/437A61K31/4545A61K31/496
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 10,537,573
App. No.
15/112,818
Granted
Jan 21, 2020
Kind
B2
Abstract

The present invention relates to combinations comprising a positive allosteric modulator (“PAM”) of metabotropic glutamatergic receptor subtype 2 (“mGluR2”) or a pharmaceutically acceptable salt or a solvate thereof, or an orthosteric agonist of metabotropic glutamatergic receptor subtype 2 compound or a pharmaceutically acceptable salt or a solvate thereof, and a synaptic vesicle protein 2A (“SV2A”) ligand.

Claims (26)

1. A method for the treatment of epilepsy comprising administering to a patient in need thereof a therapeutically effective amount of a combination comprising:

(a) a synaptic vesicle protein 2A (“SV2A”) ligand selected from the group consisting of levetiracetam, brivaracetam; and

(b) a positive allosteric modulator (“PAM”) of metabotropic glutamatergic receptor subtype 2 (“mGluR2”) compound of

or a pharmaceutically acceptable salt thereof.

2. The method of claim 1 wherein the SV2A ligand is levetiracetam.

3. The method of claim 1 wherein the SV2A ligand is brivaracetam.

4. The method of claim 1 wherein the combination of the SV2A ligand and the PAM of a mGluR2 compound is administered simultaneously to treat epilepsy.

5. The method of claim 1 wherein the combination of the SV2A ligand and the PAM of a mGluR2 compound is administered separately to treat epilepsy.

6. The method of claim 1 wherein the combination of the SV2A ligand and the PAM of a mGluR2 compound is administered sequentially to treat epilepsy.

7. The method of claim 1 wherein the epilepsy is epilepsy with partial onset seizures.

8. The method of claim 1 wherein the epilepsy is epilepsy with myoclonic seizures.

9. The method of claim 1 wherein the epilepsy is epilepsy with primary generalized tonic-clonic seizures.

10. The method of claim 1 wherein the epilepsy is treatment resistant epilepsy.

11. A method for the treatment of epilepsy comprising administering to a patient in need thereof a therapeutically effective amount of a combination comprising:

(a) a SV2A ligand selected from the group consisting of levetiracetam, brivaracetam; and

(b) a PAM of mGluR2 compound of

or a pharmaceutically acceptable salt thereof.

12. The method of claim 11 wherein the SV2A ligand is levetiracetam.

13. The method of claim 11 wherein the SV2A ligand is brivaracetam.

14. The method of claim 11 wherein the combination of the SV2A ligand and the PAM of a mGluR2 compound is administered simultaneously to treat epilepsy and related disorders.

15. The method of claim 11 wherein the combination of the SV2A ligand and the PAM of a mGluR2 compound is administered separately to treat epilepsy and related disorders.

16. The method of claim 11 wherein the combination of the SV2A ligand and the PAM of a mGluR2 compound is administered sequentially to treat epilepsy and related disorders.

17. The method of claim 11 wherein the epilepsy is epilepsy with partial onset seizures.

18. The method of claim 11 wherein the epilepsy is epilepsy with myoclonic seizures.

19. The method of claim 11 wherein the epilepsy is epilepsy with primary generalized tonic-clonic seizures.

20. The method of claim 11 wherein the epilepsy is treatment resistant epilepsy.

Assignments (5)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 20, 2016
From: KLEIN, BRIAN D; WHITE, H STEVEN
To: NEUROADJUVANTS, INC
Reel/Frame 039201/0260 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 20, 2016
From: LAVREYSEN, HILDE; PYPE, STEFAN MARIA, CHRISTIAAN; VAN OSSELAER, NANCY EULALIE, SYLVAIN; CEUSTERS, MARC
To: JANSSEN PHARMACEUTICA NV
Reel/Frame 039201/0482 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 20, 2016
From: CID-NÚÑEZ, JOSÉ MARIA; TRABANCO-SUÁREZ, ANDRÉS AVELINO
To: JANSSEN-CILAG, S.A.
Reel/Frame 039201/0749 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 20, 2016
From: TWYMAN, ROY E; BONE, ROGER FRANCIS
To: JANSSEN RESEARCH AND DEVELOPMENT, LLC.
Reel/Frame 039201/0903 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 20, 2016
From: NEUROADJUVANTS, INC.; JANSSEN RESEARCH AND DEVELOPMENT, LLC; JANSSEN-CILAG, S.A.
To: JANSSEN PHARMACEUTICA NV
Reel/Frame 039202/0037 →
Priority Claims (4)
EP 14153880 · Feb 4, 2014 · regional
EP 14153887 · Feb 4, 2014 · regional
EP 14183324 · Sep 3, 2014 · regional
EP 14187429 · Oct 2, 2014 · regional
Continuity (3)
Provisional Application 61929795 · Jan 21, 2014
Provisional Application 62091668 · Dec 15, 2014
Related Publication 20160367554A1 · Dec 22, 2016
Cited By (1)
US 12,396,981