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临床试验/NCT06261502
NCT06261502招募中2 期

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

Université de Sherbrooke1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2025年9月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
招募中
入组人数
40
试验地点
1
主要终点
Impact of Oral CBD Solution on Behavioral Inhibition

研究概览

简要总结

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.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Treatment
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

盲法说明

The randomization and participant code allocation process will be carried out by the Centre de recherche du Centre hospitalier universitaire de Sherbrooke (CRCHUS) pharmacy. The pharmacy will dispense the medication or placebo based on the randomization. The principal investigators, Drs. Lepage and Corbin and the research, as well as the participants and their caregivers, will never be aware of the randomization. To avoid any suspicions on the part of the investigators, Dr. Artuela Çaku, who is not part of the research team, will have access to the laboratory results. In the event of an adverse drug effect, Dr. Çaku may break the code to make a more informed decision for the patient's well-being, such as discontinuing participation or reducing the dose, etc.

入排标准

年龄范围
7 Years 至 40 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • 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

排除标准

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

研究组 & 干预措施

CBD First

Experimental

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.

干预措施: CBD Oral Solution (Drug)

CBD First

Experimental

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.

干预措施: Placebo (Drug)

Placebo First

Experimental

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.

干预措施: CBD Oral Solution (Drug)

Placebo First

Experimental

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.

干预措施: Placebo (Drug)

结局指标

主要结局

Impact of Oral CBD Solution on Behavioral Inhibition

时间窗: At baseline, 12 weeks, 20 weeks, and 32 weeks

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.

Impact of Oral CBD Solution anxiety.

时间窗: At baseline, 12 weeks, 20 weeks, and 32 weeks

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.

Impact of Oral CBD Solution on disruptive behavior

时间窗: At baseline, 12 weeks, 20 weeks, and 32 weeks

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.

次要结局

  • Impact of Oral CBD Solution on intracortical inhibition(At baseline, 12 weeks, 20 weeks, and 32 weeks)
  • Impact of Oral CBD Solution on intracortical facilitation(At baseline, 12 weeks, 20 weeks, and 32 weeks)
  • Impact of Oral CBD Solution on(At baseline, 12 weeks, 20 weeks, and 32 weeks)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Francois Corbin

Full professor, Department of biochemistry

Université de Sherbrooke

研究点 (1)

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