US2017209390A1PendingUtilityA1
7-oh-cannabidiol (7-oh-cbd) and/or 7-oh-cannabidivarin (7-oh-cbdv) for use in the treatment of epilepsy
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
55
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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-modified1 - 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.Join the waitlist — get patent alerts
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