IP Library Granted Patent US 10,583,096
Granted Patent B2
US 10,583,096 · App. 16/090,039 · Granted Mar 10, 2020

Use of cannabinoids in the treatment of epilepsy

View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 10,583,096
App. No.
16/090,039
Granted
Mar 10, 2020
Kind
B2
Abstract

The present invention relates to the use of cannabidiol (CBD) in the treatment of Sturge Weber syndrome. CBD appears particularly effective in reducing all types of seizures and non-seizure symptoms in patients suffering with Sturge Weber syndrome. Preferably the CBD used is in the form of a highly purified extract of cannabis such that the CBD is present at greater than 98% of the total extract (w/w) and the other components of the extract are characterised. In particular the cannabinoid tetrahydrocannabinol (THC) has been substantially removed, to a level of not more than 0.15% (w/w) and the propyl analogue of CBD, cannabidivarin, (CBDV) is present in amounts of up to 1%. Alternatively, the CBD may be a synthetically produced CBD.

Claims (19)

1. A method of treating Sturge Weber syndrome in a subject, comprising administering to the subject a therapeutically effective amount of cannabidiol (CBD), wherein the CBD is a highly purified extract of cannabis which comprises at least 98% (w/w) CBD, and wherein the CBD is administered in combination with one or more concomitant anti-epileptic drugs (AEDs).

2. The method of claim 1 , wherein the treating comprises treating seizures in a subject having Sturge Weber syndrome.

3. The method of claim 1 , wherein the treating comprises treating non-seizure symptoms in a subject having Sturge Weber syndrome.

4. The method of 3 , wherein the non-seizure symptoms are one or more of mood, behaviour, cognitive function and general quality of life.

5. The method of claim 1 , wherein the extract comprises less than 0.15% tetrahydrocannabinol (THC).

6. The method of claim 1 , wherein the extract further comprises up to 1% cannabidivarin (CBDV).

7. The method of claim 1 , wherein the extract further comprises between 0.1 and 1.0% CBDV.

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

9. The method of claim 1 , 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 a number of different AEDs that are used in combination with the CBD is reduced relative to the number of AEDs administered prior to treatment with CBD.

11. The method of claim 1 , wherein the dose of anti-epileptic drugs that are used in combination with the CBD is reduced relative to the dose of AEDs administered prior to treatment with CBD.

12. The method of claim 1 , wherein the dose of CBD is greater than 5 mg/kg/day.

13. The method of claim 1 , wherein the subject is a child or young adult.

14. The method of claim 1 , wherein the dose of CBD ranges from about 5 mg/kg/day to about 25 mg/kg/day.

15. The method of claim 2 , wherein the dose of CBD ranges from about 5 mg/kg/day to about 25 mg/kg/day.

16. The method of claim 3 , wherein the dose of CBD ranges from about 5 mg/kg/day to about 25 mg/kg/day.

17. The method of claim 1 , wherein 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.

18. The method of claim 2 , wherein 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.

19. The method of claim 3 , wherein 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.

Assignments (4)
CHANGE OF NAME Recorded Apr 21, 2025
From: GW RESEARCH LIMITED
To: JAZZ PHARMACEUTICALS RESEARCH UK LIMITED
Reel/Frame 070896/0195 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 9, 2023
From: GW PHARMA LIMITED
To: GW RESEARCH LIMITED
Reel/Frame 062932/0267 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 21, 2022
From: GUY, GEOFFREY; WRIGHT, STEPHEN; MEAD, ALICE
To: GW PHARMA LIMITED
Reel/Frame 061845/0466 →
SECURITY AGREEMENT Recorded Jul 22, 2021
From: GW PHARMA LIMITED; GW RESEARCH LIMITED
To: U.S. BANK NATIONAL ASSOCIATION
Reel/Frame 056958/0493 →