IP Library Patent Application 18642059
Patent Application
App. No. 18/642,059

TREATMENT OF IRRITABILITY IN SUBJECTS WITH AUTISM SPECTRUM DISORDERS WITH MODERATE TO SEVERE ANXIETY AND/OR SOCIAL AVOIDANCE

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 None
App. No.
18/642,059
Abstract

The present technology relates to a method of treating one or more behavioral symptoms of autism spectrum disorder (ASD) in a subject by administering an effective amount of cannabidiol (CBD). Specifically, subjects having moderate to severe ASD and relatively high social avoidance and/or anxiety are more likely to show a reduction in irritability when treated with CBD.

Claims (18)

1 . A method of treating irritability in a subject diagnosed with autism spectrum disorder (ASD), the method comprising:

administering an effective amount of cannabidiol (CBD) to the subject, wherein the subject has a high baseline ABC-C irritability score, and wherein the subject also has a high baseline ABC-CFXS social avoidance score and/or a high baseline Parent Rated Anxiety Scale for ASD (PRAS-ASD),

wherein irritability in the subject is treated.

2 . The method according to claim 1 , wherein the subject has a baseline ABC-C irritability score of greater than 12.

3 . The method according to claim 1 , wherein the subject has a baseline ABC-CFXS social avoidance score of greater than 5.

4 . The method according to claim 1 , wherein the subject has a baseline Parent Rated Anxiety Scale for ASD (PRAS-ASD) score of greater than 25.

5 . The method according to claim 1 , wherein the subject is diagnosed with moderate to severe ASD.

6 . The method according to claim 1 , wherein the subject has an Autism Diagnostic Observation Schedule, 2nd Edition (ADOS-2) comparison score of greater than or equal to 3.

7 . The method according to claim 1 , wherein the CBD is administered transdermally.

8 . The method according to claim 1 , wherein the CBD is synthetic CBD.

9 . The method according to claim 1 , wherein the CBD is botanically derived CBD.

10 . The method according to claim 1 , wherein the effective amount of CBD is a 250 mg total daily dose.

11 . The method according to claim 1 , wherein the effective amount of CBD is a 500 mg total daily dose.

12 . The method according to claim 1 , wherein the effective amount of CBD is a 750 mg total daily dose.

13 . The method according to claim 1 , wherein the effective amount of CBD is a 1000 mg total daily dose.

14 . The method according to claim 1 , wherein the effective amount is administered in two daily doses.

15 . The method according to claim 1 , wherein the CBD is administered in a pharmaceutically acceptable preparation that does not contain THC.

16 . The method according to claim 1 , wherein the subject is also diagnosed with Fragile X Syndrome (FXS).

Assignments (1)
SUPPLEMENTAL CONFIRMATORY GRANT OF SECURITY INTEREST IN UNITED STATES PATENTS Recorded May 18, 2026
From: HARMONY BIOSCIENCES MANAGEMENT, INC. (F/K/A ZYNERBA PHARMACEUTICALS, INC.)
To: JPMORGAN CHASE BANK, N.A., AS ADMINISTRATIVE AGENT
Reel/Frame 075642/0639 →