IP Library Granted Patent US 12,383,564
Granted Patent B2
US 12,383,564 · App. 18/905,534 · Granted Aug 12, 2025

Ganaxolone for use in treating tuberous sclerosis complex and seizure disorders

Inventors: Joseph Hulihan (Radnor, PA); Alex Aimetti (Radnor, PA); Scott Braunstein (Radnor, PA)
Assignee: Immedica Pharma US Inc.
A61K31/57A61K31/658A61P25/08
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Quick Facts
Patent No.
US 12,383,564
App. No.
18/905,534
Granted
Aug 12, 2025
Kind
B2
Abstract

The disclosure to methods for treating tuberous sclerosis complex and epilepsy disorders comprising administering to a subject in need thereof a therapeutically effective amount of ganaxolone or a pharmaceutically acceptable salt thereof.

Claims (24)

1. A method for treating seizures associated with Lennox-Gastaut syndrome, comprising orally administering to a subject in need thereof ganaxolone in an amount of:

about 150 mg per day for about one week, followed by about 300 mg per day for about one week, followed by about 600 mg per day for about one week, followed by about 1,200 mg per day for about one week, followed by about up to 1,800 mg per day for the remaining treatment period.

2. The method of claim 1 , wherein the subject is concomitantly being administered cannabidiol.

3. The method of claim 1 , wherein about 50 mg are administered three times a day for about one week, followed by about 100 mg administered three times a day for about one week, followed by about 200 mg administered three times a day for about one week, followed by about 400 mg administered three times a day for about one week, followed by 600 mg administered three times a day for the remaining treatment period.

4. The method of claim 3 , wherein the subject weighs more than 28 kg.

5. The method of claim 1 , wherein ganaxolone is administered as an oral suspension or oral solution.

6. The method of claim 1 , wherein ganaxolone is administered as an oral capsule or tablet.

7. The method of claim 1 , wherein the treatment period is for at least about 5 weeks or longer.

8. The method of claim 1 , wherein administration of ganaxolone does not result in somnolence in the subject.

9. The method of claim 1 , wherein administering ganaxolone reduces the frequency of seizure in the subject relative to baseline.

10. The method of claim 1 , wherein administering ganaxolone results in a reduction in seizure frequency of about 20% or greater relative to baseline seizure frequency.

11. The method of claim 1 , wherein the subject weighs more than 28 kg.

12. A method for treating seizures associated with Lennox-Gastaut syndrome, comprising orally administering to a subject in need thereof ganaxolone in an amount of:

about 6 mg/kg/day for about one week, followed by about 12 mg/kg/day for about one week, followed by about 24 mg/kg/day for about one week, followed by about 42 mg/kg/day for about one week, followed by about up to 63 mg/kg/day for the remaining treatment period.

13. The method of claim 12 , wherein about 2 mg/kg are administered three times a day for about one week, followed by about 4 mg/kg administered three times a day for about one week, followed by about 8 mg/kg administered three times a day for about one week, followed by about 14 mg/kg administered three times a day for about one week, followed by 21 mg/kg administered three times a day for the remaining treatment period.

14. The method of claim 13 , wherein the subject weighs 28 kg or less.

15. The method of claim 12 , wherein ganaxolone is administered as an oral suspension or oral solution.

16. The method of claim 12 , wherein ganaxolone is administered as an oral capsule or tablet.

17. The method of claim 12 , wherein the treatment period is for at least about 5 weeks or longer.

18. The method of claim 12 , wherein administration of ganaxolone does not result in somnolence in the subject.

19. The method of claim 12 , wherein administering ganaxolone reduces the frequency of seizure in the subject relative to baseline.

20. The method of claim 12 , wherein administering ganaxolone results in a reduction in seizure frequency of about 20% or greater relative to baseline seizure frequency.

21. The method of claim 12 , wherein the subject is concomitantly being administered cannabidiol.

22. The method of claim 12 , wherein the subject weighs 28 kg or less.

Assignments (2)
CHANGE OF NAME Recorded May 8, 2025
From: MARINUS PHARMACEUTICALS, INC.
To: IMMEDICA PHARMA US INC.
Reel/Frame 071062/0545 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 8, 2024
From: HULIHAN, JOSEPH; AIMETTI, ALEX; BRAUNSTEIN, SCOTT
To: MARINUS PHARMACEUTICALS, INC.
Reel/Frame 068824/0694 →
Continuity (5)
Continuation 18829810 · Sep 10, 2024
Continuation 18432492 · Feb 5, 2024
Continuation PCTUS2022077419 · Sep 30, 2022
Provisional Application 63252106 · Oct 4, 2021
Related Publication 20250025477A1 · Jan 23, 2025
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