IP Library Granted Patent US 10,799,485
Granted Patent B2
US 10,799,485 · App. 16/789,709 · Granted Oct 13, 2020

Methods and compositions for treatment of epileptic disorders

Inventor: Matthew During (Weston, CT)
Assignee: Ovid Therapeutics Inc.
A61K31/437A61K9/0019A61K31/165A61K31/19A61K31/195A61K31/197A61K31/27A61K31/325A61K31/36A61K31/4015A61K31/4166A61K31/4192A61K31/423A61K31/433A61K31/44A61K31/444A61K31/4535A61K31/513A61K31/515A61K31/53A61K31/55A61K31/5513A61K31/5517A61K31/57A61K31/7048A61K45/06
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Quick Facts
Patent No.
US 10,799,485
App. No.
16/789,709
Granted
Oct 13, 2020
Kind
B2
Abstract

Use of allosteric modulators and/or gaboxadol for the treatment of epileptic disorders in a subject in need thereof.

Claims (20)

1. A method of treating PCDH19 related epilepsy comprising administering to a patient in need thereof a pharmaceutical composition comprising ganaxolone or a pharmaceutically acceptable salt thereof.

2. The method of claim 1 , wherein the patient is administered ganaxolone or a pharmaceutically acceptable salt thereof twice daily.

3. The method of claim 1 , wherein the patient is administered ganaxolone or a pharmaceutically acceptable salt thereof three times daily.

4. The method of claim 1 , wherein the patient is administered ganaxolone or a pharmaceutically acceptable salt thereof in an amount of up to 1,800 mg/day.

5. The method of claim 1 , wherein the pharmaceutical composition is an oral capsule.

6. The method of claim 1 , wherein the pharmaceutical composition is an oral suspension.

7. The method of claim 1 , wherein the pharmaceutical composition is an oral suspension comprising 50 mg/ml ganaxolone or a pharmaceutically acceptable salt thereof.

8. The method of claim 1 , wherein the pharmaceutical composition is an oral suspension comprising 50 mg/ml ganaxolone or a pharmaceutically acceptable salt thereof and is administered three times daily.

9. The method of claim 1 , wherein the pharmaceutical composition is an oral suspension comprising 50 mg/ml ganaxolone or a pharmaceutically acceptable salt thereof administered three times daily wherein the patient is administered an amount of up to 1,800 mg/day.

10. The method of claim 1 , wherein the patient is administered 600 mg ganaxolone or a pharmaceutically acceptable salt thereof.

11. The method of claim 1 , wherein the patient is administered 600 mg ganaxolone or a pharmaceutically acceptable salt thereof three times daily.

12. The method of claim 1 , wherein the patient is administered 50 mg ganaxolone or a pharmaceutically acceptable salt thereof.

13. The method of claim 1 , wherein the patient is administered 100 mg ganaxolone or a pharmaceutically acceptable salt thereof.

14. The method of claim 1 , wherein the patient is administered 200 mg ganaxolone or a pharmaceutically acceptable salt thereof.

15. The method of claim 1 , wherein the patient is administered 300 mg ganaxolone or a pharmaceutically acceptable salt thereof.

16. The method of claim 1 , wherein the patient is administered 400 mg ganaxolone or a pharmaceutically acceptable salt thereof.

17. The method of claim 1 , wherein the patient is administered 500 mg ganaxolone or a pharmaceutically acceptable salt thereof.

18. The method of claim 1 , wherein the patient is administered oral capsules comprising 200-600 mg ganaxolone or a pharmaceutically acceptable salt thereof.

19. The method of claim 1 , wherein the pharmaceutical composition provides reduction in the frequency of seizures.

20. The method of claim 1 , wherein the pharmaceutical composition provides reduction in the frequency of seizures, the severity of seizures, or a combination thereof.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 3, 2020
From: DURING, MATTHEW
To: OVID THERAPEUTICS INC.
Reel/Frame 053685/0303 →
Continuity (7)
Continuation 16447300 · Jun 20, 2019
Continuation 16356517 · Mar 18, 2019
Continuation 16013500 · Jun 20, 2018
Continuation 15673737 · Aug 10, 2017
Provisional Application 62490293 · Apr 26, 2017
Provisional Application 62373589 · Aug 11, 2016
Related Publication 20200179350A1 · Jun 11, 2020