IP Library Granted Patent US 10,709,671
Granted Patent B2
US 10,709,671 · App. 15/183,947 · Granted Jul 14, 2020

Use of cannabinoids in the treatment of epilepsy

Inventors: Geoffrey Guy (Cambridge, GB); Stephen Wright (Cambridge, 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 10,709,671
App. No.
15/183,947
Filed
Jun 16, 2016
Granted
Jul 14, 2020
Kind
B2
Art Unit
1629
USPC
514/485
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 (24)

1. A method of treating focal seizures in Dravet Syndrome, comprising administering to a subject in need thereof cannabidiol (CBD), wherein the CBD has a purity of at least 98% (w/w) and comprises no more than 0.15% (w/w) Δ9-tetrahydrocannabidiol, wherein the CBD is administered at a dose of from 15 mg/kg/day to 20 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 up to 1% cannabidivarin (CBDV).

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

8. 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.

9. The method of claim 1 , wherein the CBD is administered as an oral composition comprising cannabidiol (CBD), a solvent, a co-solvent, a sweetener, and a flavouring.

10. The method of claim 9 , wherein the solvent is sesame oil.

11. The method of claim 9 , wherein the co-solvent is ethanol.

12. The method of claim 9 , wherein the sweetener is sucralose.

13. The method of claim 9 , wherein the flavouring is strawberry flavour.

14. The method of claim 9 , wherein the CBD is present at a concentration of between 25 mg/ml and 100 mg/ml.

15. The method of claim 9 , wherein the composition comprises cannabidiol (CBD) at a concentration of between 25 to 100 mg/ml, ethanol as co-solvent at a concentration of 79 mg/ml, sucralose as sweetener at a concentration of 0.5 mg/ml, strawberry flavouring as flavouring at a concentration of 0.2 mg/ml, and sesame oil as solvent q.s. to 1.0 ml.

16. A method of treating focal seizures in Dravet Syndrome, comprising administering to a subject in need thereof cannabidiol (CBD), wherein the CBD has a purity of at least 98% (w/w) and comprises no more than 0.15% (w/w) Δ9-tetrahydrocannabidiol, wherein the CBD is administered at a dose of 20 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 is administered in combination with one or more concomitant anti-epileptic drugs (AED).

20. The method of claim 16 , wherein the CBD is a highly purified extract of cannabis.

21. The method of claim 20 , wherein the highly purified extract further comprises up to 1% cannabidivarin (CBDV).

22. The method of claim 16 , wherein the CBD is present as a synthetic compound.

23. The method of claim 19 , 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.

24. The method of claim 16 , wherein the CBD is administered as an oral composition comprising cannabidiol (CBD), a solvent, a co-solvent, a sweetener, and a flavouring.

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 Aug 16, 2017
From: GUY, GEOFFREY; WRIGHT, STEPHEN; MEAD, ALICE; CHEETHAM, EMMA; DEVINSKY, ORRIN; SCHILLER, DOMINIC
To: GW RESEARCH LIMITED
Reel/Frame 043304/0121 →
Priority Claims (1)
GB 1510664.4 · Jun 17, 2015 · national
Continuity (1)
Related Publication 20170007551A1 · Jan 12, 2017
Cited By (25)
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