Use of cannabinoids in the treatment of epilepsy
US-9474726-B2 · Oct 25, 2016 · US
US11147776B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11147776-B2 |
| Application number | US-201916591702-A |
| Country | US |
| Kind code | B2 |
| Filing date | Oct 3, 2019 |
| Priority date | Jun 27, 2014 |
| Publication date | Oct 19, 2021 |
| Grant date | Oct 19, 2021 |
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The present invention relates to the use of 7-hydroxy-cannabidol (7-OH-CBD) and/or 7-hydroxy-cannabidivarin (7-OH-CBDV) in the treatment of epilepsy. Preferably the cannabinoid metabolites are isolated from plants to produce a highly purified extract or can be reproduced synthetically.
Opening claim text (preview).
The invention claimed is: 1. A method of treating tonic-clonic seizures in a subject with epilepsy comprising administering a therapeutically effective amount of 7-hydroxy-cannabidiol (7-OH-CBD), thereby treating tonic-clonic seizures. 2. The method of claim 1 , wherein the 7-OH-CBD is in a pure, isolated or synthetic form. 3. The method of claim 1 , further comprising administering to the subject a therapeutically effective amount of 7-hydroxy-cannabidivarin (7-OH-CBDV). 4. The method of claim 1 , wherein the 7-OH-CBD is administered as a pharmaceutical composition comprising the 7-OH-CBD with a pharmaceutically acceptable carrier. 5. The method of claim 1 , further comprising administering to the subject one or more concomitant anti-epileptic drugs (AED). 6. The method of claim 5 , wherein the one or more AED is selected from the group consisting of: clobazam; levetiracetam; topiramate; stiripentol; phenobarbital; lacsamide; valproic acid; zonisamide; perampanel; and fosphenytoin. 7. The method of claim 1 , wherein the dose of 7-OH-CBD is between 1 and 2000 mg/kg. 8. The method of claim 3 , wherein the 7-OH-CBD is formulated for administration separately, sequentially or simultaneously with the 7-OH-CBDV or the combination is provided in a single dosage form. 9. The method of claim 3 , wherein the 7-OH-CBDV is in a pure, isolated or synthetic form. 10. The method of claim 3 , wherein the dose of 7-OH-CBDV is between 1 and 2000 mg/kg. 11. The method of claim 4 , wherein the pharmaceutical composition further comprises 7-hydroxy-cannabidivarin (7-OH-CBDV). 12. A pharmaceutical composition comprising 7-hydroxy-cannabidiol (7-OH-CBD) with a pharmaceutically acceptable carrier. 13. The pharmaceutical composition of claim 12 , wherein the pharmaceutical composition further comprises 7-hydroxy-cannabidivarin (7-OH-CBDV). 14. The pharmaceutical composition of claim 12 , wherein the 7-OH-CBD is in a pure, isolated or synthetic form. 15. The pharmaceutical composition of claim 12 , wherein the composition is formulated to have a dose of 7-OH-CBD between 1 and 2000 mg/kg. 16. The pharmaceutical composition of claim 13 , wherein the 7-OH-CBD is formulated for administration separately, sequentially or simultaneously with the 7-OH-CBDV. 17. The pharmaceutical composition of claim 13 , wherein the 7-OH-CBD and 7-OH-CBDV are provided in a single dosage form. 18. The method of claim 1 , wherein the 7-OH-CBD is administered in an oral solution comprising the 7-OH-CBD and a pharmaceutically acceptable carrier. 19. The method of claim 1 , wherein the administering treats myoclonic jerks. 20. The method of claim 1 , wherein the administering reduces seizure severity. 21. The method of claim 1 , wherein the administering reduces latency to seizure onset.
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o-phenolic cannabinoids, e.g. cannabidiol, cannabigerolic acid, cannabichromene or tetrahydrocannabinol · CPC title
Injectable compositions; Intramuscular, intravenous, arterial, subcutaneous administration; Compositions to be administered through the skin in an invasive manner (non-active ingredients are additionally classified in A61K47/00) · CPC title
Solutions {(composition of solutions A61K47/00)} · CPC title
Alcohols; Phenols; Salts thereof, e.g. glycerol; Polyethylene glycols [PEG]; Poloxamers; PEG/POE alkyl ethers · CPC title
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