US2017209390A1PendingUtilityA1

7-oh-cannabidiol (7-oh-cbd) and/or 7-oh-cannabidivarin (7-oh-cbdv) for use in the treatment of epilepsy

Assignee: GW PHARMA LTDPriority: Jun 27, 2014Filed: Jun 29, 2015Published: Jul 27, 2017
Est. expiryJun 27, 2034(~7.9 yrs left)· nominal 20-yr term from priority
A61K 9/08A61K 9/0019A61K 47/44A61K 47/10A61K 45/06A61P 25/08A61K 36/3482A61K 31/658A61K 31/05
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Claims

Abstract

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.

Claims

exact text as granted — not AI-modified
1 - 7 . (canceled) 
     
     
         8 . A method of treating epilepsy, the method comprising administering to a subject in need thereof a therapeutically effective amount of 7-hydroxy-cannabidivarin (7-OH-CBDV) 
     
     
         9 . The method as claimed in  claim 8 , wherein the 7-OH-CBDV is in a pure, isolated or synthetic form. 
     
     
         10 . The method as claimed in  claim 8 , further comprising administering to the subject a therapeutically effective amount of 7-hydroxy-cannabidiol (7-OH-CBD). 
     
     
         11 . The method as claimed in  claim 8 , wherein the 7-OH-CBDV is administered as a pharmaceutical composition comprising the 7-OH-CBDV with a pharmaceutically acceptable carrier. 
     
     
         12 . The method as claimed in  claim 8 , further comprising administering to the subject one or more concomitant anti-epileptic drugs (AED). 
     
     
         13 . The method as claimed in  claim 12 , 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. 
     
     
         14 . The method as claimed in  claim 8 , wherein the dose of 7-OH-CBDV is between 1 and 2000 mg/kg. 
     
     
         15 . The method as claimed in  claim 10 , wherein the 7-OH-CBDV is formulated for administration separately, sequentially or simultaneously with the 7-OH-CBD or the combination is provided in a single dosage form. 
     
     
         16 . The method of  claim 10 , wherein the 7-OH-CBD is in a pure, isolated or synthetic form. 
     
     
         17 . The method of  claim 10 , wherein the dose of 7-OH-CBD is between 1 and 2000 mg/kg. 
     
     
         18 . The method of  claim 11 , wherein the pharmaceutical composition further comprises 7-hydroxy-cannabidiol (7-OH-CBD). 
     
     
         19 . A pharmaceutical composition comprising 7-hydroxy-cannabidivarin (7-OH-CBDV) with a pharmaceutically acceptable carrier.

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