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RecruitingNCT06261502CANAXUpdated Aug 28, 2026

Effect of CANnabidiol on Anxiety and GABAergic Function in Individuals With Fragile-X Syndrome

A Phase 2 interventional study of CBD Oral Solution and Placebo in Fragile X Syndrome, sponsored by Université de Sherbrooke. Recruiting at 1 site in Canada. Open to participants aged 7 Years to 40 Years. Per ClinicalTrials.gov, last updated 2026-08-28.

Sponsored by Université de Sherbrooke · Phase 2, Interventional, and Treatment

From the registry’s dates

  • Started Sep 2025; still recruiting 1 year 2 months later.
Phase
Phase 2
Study type
Interventional
Enrollment
40
Allocation
Randomized
Ages
7 Years to 40 Years
Sex
All
01

Study summary

This study focuses on the therapeutic relevance of the endocannabinoid (eCB) system for the treatment of Fragile-X syndrome (FXS), the primary hereditary cause of autism spectrum disorder (ASD). Most individuals with FXS have moderate to severe intellectual disability (ID), and caregivers are mainly concerned about aggressive behavior and anxiety problems. Since FXS individuals have a normal lifespan, the overall lifetime cost for the Canadian society of a single case is estimated at $1.2 to $4.7 millions reaching $18 billions for all FXS cases. There is no cure for FXS, as all clinical trials so far have been unsuccessful.FXS is caused by transcriptional silencing of the Fragile X mental retardation protein (FMR1) gene, making FXS a simple model to study ASD and ID pathophysiological mechanisms. Of those, neuronal hyperexcitability is largely recognized as a core deficit in FXS, and a critical therapeutic target for the disorder. Using transcranial magnetic stimulation (TMS) in FXS patients, our team provided the first direct evidence of Gamma-aminobutyric acid (GABA) receptor a (GABAa) dysfunctions in humans with this disorder and showed that this inhibitory deficit is linked with cortical hyperexcitability (PMID: 31748507). Concurrent lines of evidence suggest that stimulation of the endocannabinoid (eCB) system with the administration of Cannabidiol (CBD) could upregulate GABAergic function and correct inhibitory deficits presumed responsible for the neuropsychiatric phenotype of FXS. CBD has been shown to increase GABA concentration levels in the brains of healthy individuals, an effect that could help correct the hyperexcitability typically found in FXS. Thus, this trial aims to define the therapeutic potential of the eCB system for FXS, by measuring the impacts of oral CBD administration on the principal inhibitory neurotransmitter system of FXS patients, and the severity of the clinical phenotype.

02

Conditions studied

  • Fragile X Syndrome

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Keywords

  • FXS
  • CBD
  • TMS
  • MRI
  • eCB
03

In context

Fragile X Syndrome

114 studies on the registry are indexed under Fragile X Syndrome; 24 are open to participants now.

This study's planned enrollment of 40 is below the median of 50 across 91 interventional studies indexed under Fragile X Syndrome.

Browse Fragile X Syndrome studies →

Lead sponsor

Université de Sherbrooke is the lead sponsor of 295 studies on the registry; 65 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
7 Years to 40 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Molecular diagnosis of FXS
  • Age 7 to 40 inclusively
  • Overall ABC-C score > 20
  • Taking up to 3 psychoactive drugs
  • No therapeutic change for the last 3 months

Exclusion criteria

Exclusion Criteria:

  • Taking valproic acid
  • Taking clobazam
  • History of liver problems
  • (AST) or alanine transaminase (ALT), > 3 times the reference values
  • > 2 times the reference values
  • Absolute to the use of TMS and MRI (e.g. presence of metal in the body), will also be considered as an exclusion criterion.
Terms in these criteria, in plain language(3)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

ALT and AST (liver enzymes)

Two enzymes measured in a routine blood test of the liver. Higher levels can mean the liver is under strain or damaged. SGPT and SGOT are older names for ALT and AST.

Criteria usually give a limit as a multiple of the upper limit of normal (ULN), often higher when cancer has spread to the liver.

Bilirubin

A yellow substance made when red blood cells are broken down, which the liver clears. A high level can mean a problem with the liver or the bile ducts.

Criteria often allow more for people with Gilbert’s syndrome, a harmless inherited condition that raises bilirubin.

Contraindication

A reason a treatment, test or procedure should not be given to a particular person, such as an allergy, another illness or a medicine they take.

05

Study design

Phase
Phase 2
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Crossover assignment
Masking
Quadruple (Participant, Care provider, Investigator, Outcomes assessor)
Enrollment
40 participants (estimated)

Study arms

  • Experimental
    CBD First

    Participants will start with CBD to stimulate the eCB for 12 weeks, undergo an 8-week washout period, and then receive a 12-week placebo.

    Drug: CBD Oral Solution · Drug: Placebo

  • Experimental
    Placebo First

    Participants will start with a placebo for 12 weeks, undergo an 8-week washout period, and then receive a 12-week CBD to stimulate the eCB system.

    Drug: CBD Oral Solution · Drug: Placebo

Interventions

  • Participants will start with oral CBD dose of 5 mg/kg/day for two weeks and then increase to 10 mg/kg/day.

  • DrugPlacebo

    Participants will receive a dose of a placebo composed of the inactive ingredients of CBD of the same volume as the CBD Oral Solution.

06

What researchers measure

Primary outcomes

  1. Impact of Oral CBD Solution anxiety.

    Caregivers will complete The Anxiety, Depression, and Mood Scale (ADAMS). The ADAMS consists of 29 items on a 4-point scale from 0 (behavior have not occurred or is not a problem) to 3 (behavior occurs a lot, or is a severe problem). It evaluates emotional disturbances along five dimensions: mania/hyperactivity, depressed mood, social avoidance, general anxiety, and obsessive behavior.

    Time frame: At baseline, 12 weeks, 20 weeks, and 32 weeks

  2. Impact of Oral CBD Solution on disruptive behavior

    Caregivers will complete the Aberrant Behavior Checklist-Community Fragile-X (ABC-C FX). The ABC-C FX has 55 items and is subdivided into explores 6 subdomains: irritability, hyperactivity, lethargy/withdrawal, stereotypy, inappropriate speech, and social avoidance. Higher scores reflect higher aberrant behavior. ABC-C FX is considered the gold standard for assessing behavioral changes in clinical trials in FXS.

    Time frame: At baseline, 12 weeks, 20 weeks, and 32 weeks

  3. Impact of Oral CBD Solution on Behavioral Inhibition

    Participants will complete the NIH Toolbox Cognitive Battery Flanker Task, a behavioral inhibition task validated in FXS. Global scores range from 0 to 10 and are algorithmically defined using accuracy and reaction time. Higher scores reflect better performance.

    Time frame: At baseline, 12 weeks, 20 weeks, and 32 weeks

Secondary outcomes

  1. Impact of Oral CBD Solution on intracortical inhibition

    TMS-derived measure of Intracortical inhibition: The degree of decrease of peak-to-peak motor evoked potential (MEP) amplitude induced by the administration of a conditioning stimulus (set at 70% of resting motor threshold) 2-4 ms before the test stimulus (stimulation intensity required to produce an MEP of 1 millivolt (mV), approximately 120% of resting motor threshold)

    Time frame: At baseline, 12 weeks, 20 weeks, and 32 weeks

  2. Impact of Oral CBD Solution on intracortical facilitation

    Transcranial magnetic stimulation (TMS) -derived measure of Intracortical facilitation: The degree of increase of peak-to-peak motor evoked potential (MEP) amplitude induced by the administration of a conditioning stimulus (set at 80% of resting motor threshold) 12-24 ms before the test stimulus (stimulation intensity required to produce an MEP of 1 mV, approximately 120% of resting motor threshold).

    Time frame: At baseline, 12 weeks, 20 weeks, and 32 weeks

  3. Impact of Oral CBD Solution on

    Estimation of GABA concentrations in the brain from magnetic resonance spectroscopy

    Time frame: At baseline, 12 weeks, 20 weeks, and 32 weeks

07

Study locations

1 of 1 sites recruiting
  • Universite de Sherbrooke, CHUS Research Center
    Sherbrooke, Quebec J1H5N4, Canada
    Recruiting
    • Francois Corbin, MD/PhD · Contactfrancois.corbin@usherbrooke.ca · 819-346-1110
    • Amanda Andrews, B.A. · Contact819-346-1110
    • Jean-Francois Lepage, Ph.D. · Principal investigator
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Started Sep 2025 (actual). Primary completion is estimated for Jul 2028, 34 months after the start.

Of 15 phase 2 interventional studies under Fragile X Syndrome, half reached primary completion within 24 months of starting (the median), counting those still running; a quarter within 15 and three quarters within 37. This study's planned 34 months is above that.

How these figures are worked out, and which studies are left out of them.

Registered
Jan 26, 2024
First posted
Feb 15, 2024
StartActual
Sep 1, 2025
Primary completionEst.
Jul 1, 2028
CompletionEst.
Dec 1, 2028
Last update
Aug 28, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Aug 28, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06261502
Collaborators
Canadian Institutes of Health Research (CIHR), Jazz Pharmaceuticals, Centre de recherche du Centre hospitalier universitaire de Sherbrooke
Responsible party
Francois Corbin (Full professor, Department of biochemistry, Université de Sherbrooke) — Principal investigator
First posted
Feb 15, 2024
Start date
Sep 1, 2025
Primary completion
Jul 1, 2028 (estimated)
Completion
Dec 1, 2028 (estimated)
Last update
Aug 28, 2026

Study contacts

François Corbin, MD, Ph.D.
Contact
Francois.Corbin@USherbrooke.ca
819-346-1110 ext. 15801
Amanda Andrews, B.A.
Contact
amanda.andrews@usherbrooke.ca
819-346-1110

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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