IP Library › Granted Patent US 11,369,606
Granted Patent B2
US 11,369,606 · App. 16/720,750 · Granted Jun 28, 2022

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

Inventors: Brian D. Klein (Potomac Maryland, 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
A61K31/506A61K9/4858A61K31/381A61K31/4015A61K31/437A61K31/4545A61K31/496A61K45/06A61P25/02A61P25/06A61P25/08A61P25/18
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Quick Facts
Patent No.
US 11,369,606
App. No.
16/720,750
Granted
Jun 28, 2022
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 (24)

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

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

(b)

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 SV2A ligand and Compound 6b or a pharmaceutically acceptable salt thereof are administered simultaneously.

5. The method of claim 1 wherein the SV2A ligand and Compound 6b or a pharmaceutically acceptable salt thereof are administered separately.

6. The method of claim 1 wherein the SV2A ligand and Compound 6b or a pharmaceutically acceptable salt thereof are administered sequentially.

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

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

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

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

11. The method of claim 1 , comprising administering to the patient a therapeutically effective amount of (a) the SV2A ligand; and

(b) Compound 6b.

12. The method of claim 11 wherein the SV 2 A ligand is levetiracetam.

13. The method of claim 11 wherein the SV 2 A ligand is brivaracetam.

14. The method of claim 11 wherein the SV 2 A ligand and Compound 6 b or a pharmaceutically acceptable salt thereof are administered simultaneously.

15. The method of claim 11 wherein the SV2A ligand and Compound 6 b or a pharmaceutically acceptable salt thereof are administered separately.

16. The method of claim 11 wherein the SV2A ligand and Compound 6 b or a pharmaceutically acceptable salt thereof are administered sequentially.

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

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

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

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

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 (4)
Continuation 15112818
Provisional Application 61929795 · Jan 21, 2014
Provisional Application 62091668 · Dec 15, 2014
Related Publication 20200138814A1 · May 7, 2020
Cited By (1)
US 12,396,981