跳至主要内容
临床试验/NCT03202303
NCT03202303招募中2 期

Cannabidivarin (CBDV) vs. Placebo in Children With Autism Spectrum Disorder (ASD)

Montefiore Medical Center2 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2019年4月12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
100
试验地点
2
主要终点
Aberrant Behavior Checklist-Irritability (ABC-I) Subscale

研究概览

简要总结

This trial aims to study the efficacy and safety of cannabidivarin (CBDV) in children with ASD.

详细描述

There is a clear unmet need for new therapeutics to treat irritability in children with ASD that do not have the metabolic and weight adverse event profiles of the currently approved treatments. Cannabidivarin (CBDV) is a nonpsychoactive phytocannabinoid and a safe variant of Cannabidiol (CBD). It has no appreciable tetrahydrocannabinol (THC) [less than 0.01%], has been shown to have no impact on weight or metabolism, and improves both social and cognitive functioning in animal models of idiopathic and syndromal autism (Fragile X, Rett Syndrome, Angelman Syndrome). The CDC currently estimates 1 in 59 children have ASD. ASD is characterized by deficits in social communication, irritability, repetitive behaviors, impulsivity, temper tantrums, and high caregiver burden. Currently, the only FDA-approved medications for symptoms of ASD are aripiprazole and risperidone, both of which are indicated for irritability in pediatric ASD. These medications are effective but are associated with considerable side effects with long term treatment in this chronic developmental disorder, including weight gain, metabolic syndrome and the risk of type 2 diabetes, prolactin elevation and growth of breast tissue, extrapyramidal symptoms and the risk of tardive dyskinesia. The anticonvulsant divalproex sodium (valproate/VPA) also significantly reduces irritability and repetitive behaviors in individuals with ASD. Although VPA is efficacious for pediatric epilepsy and some symptoms of ASD, it also has significant side effects, including weight gain, sedation and nausea. CBDV, like VPA, is effective in the treatment of pediatric epilepsy, and ASD mouse models demonstrate potential mechanisms for treatment with CBDV, including potential therapeutic effects on repetitive behaviors, irritability, sociability, and quality of life, and the capacity to reduce inflammation. This study aims to examine the efficacy and safety of cannabidivarin (CBDV) with a primary aim of studying its effect on irritability in children with ASD.

STUDY DESIGN: This is a 12-week randomized, double-blind study of CBDV vs. placebo in 100 child and adolescent subjects aged 5 to 18 years with a diagnosis of ASD.

研究设计

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

盲法说明

Double-Blind

入排标准

年龄范围
5 Years 至 18 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

研究组 & 干预措施

Cannabidivarin (CBDV)

Experimental

Weight-based dosing of 10 mg/kg/day of CBDV for 12 weeks

干预措施: Cannabidivarin (Drug)

Matched Placebo

Placebo Comparator

Weight-based dosing of 10 mg/kg/day of placebo for 12 weeks

干预措施: Matched Placebo (Drug)

结局指标

主要结局

Aberrant Behavior Checklist-Irritability (ABC-I) Subscale

时间窗: Change from Baseline to Week 12 (Change over 12 weeks)

Change in aberrant behavior from baseline will be assessed using the irritability subscale of the ABC. The ABC is an informative rating instrument that was empirically derived by principal component analysis to measure behavior in those with developmental disability and autism spectrum disorder (ASD). The ABC-I will be completed by any adult who knows the patient well, such as a parent/caregiver. The ABC-I subscale consists of 15 items that address the presence of aggression, tantrums, and/or self-injury. Scores for each item on the subscale range from 0 (no problem at all) to 3 (problem is severe in degree), yielding an overall possible score for the subscale from 0-45, such that higher scores are indicative of increased severity of irritability. Scores will be summarized by study arm using basic descriptive statistics.

次要结局

  • Repetitive Behavior Scale-Revised (RBS-R)(Change in RBS-R from Baseline to Week 12 (Change over 12 weeks))
  • Montefiore Einstein Rigidity Scale-Revised (MERS-R)(Change in MERS-R from Baseline to Week 12 (Change over 12 weeks))
  • Aberrant Behavior Checklist-Social Withdrawal (ABC-SW) Subscale(Change in ABC-SW from Baseline to Week 12 (Change over 12 weeks))
  • Pediatric Quality of Life Inventory (PedsQL) Family Impact Module(Change in PedsQL from Baseline to Week 12 (Change over 12 weeks))
  • Vineland Adaptive Behavior Scale, Third Edition (VABS-3)(Change in VABS-3 from Baseline to Week 12 (Change over 12 weeks))
  • Clinical Global Impressions - Improvement (CGI-I)(Change in CGI-I from Baseline to Week 12 (Change over 12 weeks))

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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