IP Library Granted Patent US 12,150,927
Granted Patent B2
US 12,150,927 · App. 17/128,458 · Granted Nov 26, 2024

Use of cannabidiolic acid in the treatment of autism spectrum disorder and associated disorders

Inventors: Geoffrey Guy (Cambridge, GB); Stephen Wright (Cambridge, GB); James Brodie (Cambridge, GB); Marie Woolley-Roberts (Cambridge, GB); Rafael Maldonado (Barcelona, ES); Daniela Parolaro (Varese, IT); Livio Luongo (Naples, IT)
Assignee: GW Research Limited
A61K31/352A61K31/05A61K36/185A61K45/06A61P43/00
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Quick Facts
Patent No.
US 12,150,927
App. No.
17/128,458
Granted
Nov 26, 2024
Kind
B2
Abstract

The present invention relates to the use of cannabidiolic acid (CBDA) in the treatment of autism spectrum disorder (ASD) and ASD-associated disorders, such as Fragile X syndrome (FXS); Rett syndrome (RS); or Angelman syndrome (AS). CBDA has been shown to be particularly effective in improving cognitive dysfunction in rodent models of ASD, FXS, RS and AS. The CBDA is preferably substantially pure. It may take the form of a highly purified extract of cannabis such that the CBDA is present at greater than 95% of the total extract (w/w) and the other components of the extract are characterised. Alternatively, the CBDA is synthetically produced.

Claims (6)

1. A method for treating cognitive dysfunction in a subject in need thereof, the method comprising administering a therapeutically effective amount of cannabidiolic acid (CBDA) to the subject, wherein the CBDA is present as a highly purified extract of cannabis which comprises at least 95% w/w CBDA, or is present as a synthetic CBDA and wherein cognitive dysfunction is a dysfunction of short or long term memory loss.

2. The method according to claim 1 , wherein the cognitive dysfunction is cognitive dysfunction in an autistic spectrum disorder (ASD) or in an ASD-associated disorder.

3. The method according to claim 1 , wherein the extract comprises less than 0.15% THC.

4. The method according to claim 1 , wherein the dose of CBDA is greater than 0.01 mg/kg/day.

5. The method according to claim 4 , wherein the dose of CBDA is between 1 to 30 mg/kg/day.

6. The method according to claim 1 , wherein the CBDA is administered as an oral formulation.

Assignments (2)
CHANGE OF NAME Recorded Dec 11, 2025
From: GW RESEARCH LIMITED
To: JAZZ PHARMACEUTICALS RESEARCH UK LIMITED
Reel/Frame 073191/0407 →
SECURITY AGREEMENT Recorded Jul 22, 2021
From: GW PHARMA LIMITED; GW RESEARCH LIMITED
To: U.S. BANK NATIONAL ASSOCIATION
Reel/Frame 056958/0493 →