IP Library Granted Patent US 11,357,741
Granted Patent B2
US 11,357,741 · App. 16/893,018 · Granted Jun 14, 2022

Use of cannabinoids in the treatment of epilepsy

Inventors: Geoffrey Guy (Cambridge, GB); Stephen Wright (London, GB); Orrin Devinsky (New York, NY)
Assignee: GW Research Limited
A61K31/05A61K31/352A61K31/5513A61K36/185A61K45/06A61K47/10A61K47/26A61K47/44
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Quick Facts
Patent No.
US 11,357,741
App. No.
16/893,018
Granted
Jun 14, 2022
Kind
B2
Abstract

The present invention relates to the use of cannabidiol (CBD) in the treatment of focal seizures. In one embodiment the patients suffering from focal seizures are children and young adults. CBD appears particularly effective in reducing focal seizures in patients suffering with etiologies that include: Lennox-Gastaut Syndrome; Tuberous Sclerosis Complex; Dravet Syndrome; CDKL5; Neuronal ceroid lipofuscinoses (NCL); febrile infection related epilepsy syndrome (FIRES); Aicardi syndrome and brain abnormalities in comparison to other seizure types. Significantly CBD additionally is very effective in the reduction of a sub-type of focal seizures, focal seizures with impairment.

Claims (28)

1. A method of treating focal seizures in Dravet Syndrome, comprising administering to a subject in need thereof a drug product comprising a cannabidiol (CBD) drug substance, wherein the CBD drug substance has a purity of at least 98% (w/w), wherein the CBD is administered at a dose ranging from about 5 mg/kg/day to about 25 mg/kg/day.

2. The method of claim 1 , wherein the focal seizures are focal seizures with impairment.

3. The method of claim 1 , wherein the Dravet Syndrome is treatment-resistant.

4. The method of claim 1 , wherein the CBD is administered in combination with one or more concomitant anti-epileptic drugs (AED).

5. The method of claim 1 , wherein the CBD is a highly purified extract of cannabis.

6. The method of claim 5 , wherein the highly purified extract further comprises less than 0.15% tetrahydrocannabinol (THC).

7. The method of claim 5 , wherein the highly purified extract further comprises up to 1% (w/w) cannabidivarin (CBDV).

8. The method of claim 1 , wherein the CBD is present as a synthetic compound.

9. The method of claim 4 , wherein the one or more AED is selected from the group consisting of: carbamezapine, clobazam, clonazepam, clonidine, clorazepate, desmethylclobazam, diazepam, ethosuximide, felbamate, ketogenic diet, lacosamide, lamotrigine, levetiracetam, lorazepam, midazolam, N-desmethylclobazam, nordiazepam, oxycarbamezapine, perampanel, phenobarbital, phenytoin, pregabalin, rufinamide, stiripentol, topiramate, trazodone, vagus nerve stimulation, valproic acid, vigabatrin, and zonisamide.

10. The method of claim 1 , wherein the dose of the CBD is increased to about 10 mg/kg/day.

11. The method of claim 1 , wherein the dose of the CBD is increased to about 12 mg/kg/day.

12. The method of claim 1 , wherein the dose of the CBD is increased to about 14 mg/kg/day.

13. The method of claim 1 , wherein the dose of the CBD is increased to about 15 mg/kg/day.

14. The method of claim 1 , wherein the dose of the CBD is increased to about 18 mg/kg/day.

15. The method of claim 1 , wherein the dose of the CBD is increased to about 20 mg/kg/day.

16. A method of treating focal seizures in Dravet Syndrome, comprising administering to a subject in need thereof a drug product comprising a cannabidiol (CBD) drug substance, wherein the CBD drug substance has a purity of at least 98% (w/w), and the CBD is administered at a dose of 5 mg/kg/day, and then the dose is increased by 2 to 5 mg/kg increments, up to 25 mg/kg/day.

17. The method of claim 16 , wherein the focal seizures are focal seizures with impairment.

18. The method of claim 16 , wherein the Dravet Syndrome is treatment-resistant.

19. The method of claim 16 , wherein the CBD comprises Δ9-tetrahydrocannabinol (THC).

20. The method of claim 19 , wherein the CBD comprises not more than 0.15% (w/w) Δ9-tetrahydrocannabinol (THC).

21. The method of claim 16 , wherein the dose of the CBD is increased to about 10 mg/kg/day.

22. The method of claim 16 , wherein the dose of the CBD is increased to about 12 mg/kg/day.

23. The method of claim 16 , wherein the dose of the CBD is increased to about 14 mg/kg/day.

24. The method of claim 16 , wherein the dose of the CBD is increased to about 15 mg/kg/day.

25. The method of claim 16 , wherein the dose of the CBD is increased to about 18 mg/kg/day.

26. The method of claim 16 , wherein the dose of the CBD is increased to about 20 mg/kg/day.

27. The method of claim 16 , wherein the CBD is administered in combination with one or more concomitant anti-epileptic drugs (AED).

28. The method of claim 27 , wherein the one or more AED is selected from the group consisting of: carbamezapine, clobazam, clonazepam, clonidine, clorazepate, desmethylclobazam, diazepam, ethosuximide, felbamate, ketogenic diet, lacosamide, lamotrigine, levetiracetam, lorazepam, midazolam, N-desmethylclobazam, nordiazepam, oxycarbamezapine, perampanel, phenobarbital, phenytoin, pregabalin, rufinamide, stiripentol, topiramate, trazodone, vagus nerve stimulation, valproic acid, vigabatrin, and zonisamide.

Assignments (3)
CHANGE OF NAME Recorded May 16, 2024
From: GW RESEARCH LIMITED
To: JAZZ PHARMACEUTICALS RESEARCH UK LIMITED
Reel/Frame 067437/0875 →
SECURITY AGREEMENT Recorded Jul 22, 2021
From: GW PHARMA LIMITED; GW RESEARCH LIMITED
To: U.S. BANK NATIONAL ASSOCIATION
Reel/Frame 056958/0493 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 3, 2021
From: GUY, GEOFFREY; WRIGHT, STEPHEN; DEVINSKY, ORRIN
To: GW RESEARCH LIMITED
Reel/Frame 055128/0279 →