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Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be younger than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to 5 years
Summary
This trial is testing a new medication called GWP42003-P to see if it can help reduce symptoms in children with Autism Spectrum Disorder (ASD). The goal is to find out if this medication can make managing ASD easier for these children.
Who is the study for?
This trial is for children and adolescents with Autism Spectrum Disorder (ASD) who are moderately ill, weigh at least 12 kg, have an IQ of 70 or higher, and stable ASD-related treatments. They must be able to swallow liquid medication and not have other dominating conditions like ADHD or a history of substance abuse. Participants cannot be taking certain medications like clobazam or more than two anti-epileptic drugs.
What is being tested?
The study tests the effectiveness of Cannabidiol Oral Solution (GWP42003-P; CBD-OS) versus a placebo in reducing symptoms of ASD in children. It's designed to see if this treatment can help manage the condition better compared to not receiving the active drug.
What are the potential side effects?
While specific side effects aren't listed here, potential side effects may include reactions related to cannabidiol such as changes in appetite, mood alterations, drowsiness, digestive issues, and possible allergic reactions due to any excipients present in the solution.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ up to 5 years
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to 5 years
Treatment Details
Side effects data
From 2016 Phase 3 trial • 225 Patients • NCT0222456030%
Somnolence
26%
Decreased appetite
15%
Diarrhoea
12%
Upper respiratory tract infection
12%
Vomiting
11%
Pyrexia
11%
Nasopharyngitis
10%
Fatigue
6%
Headache
6%
Convulsion
6%
Lethargy
5%
Status epilepticus
5%
Insomnia
5%
Irritability
2%
Pneumonia
1%
Lymphopenia
1%
Constipation
1%
Pneumatosis intestinalis
1%
Adenovirus infection
1%
Pneumonia mycoplasmal
1%
Respiratory syncytial virus infection
1%
Delayed recovery from anaesthesia
1%
Aspartate aminotransferase increased
1%
Alanine aminotransferase increased
1%
Gamma-glutamyltransferase increased
1%
Pleural effusion
1%
Device malfunction
1%
Hypotension
100%
80%
60%
40%
20%
0%
Study treatment Arm
GWP42003-P 20 mg/kg/Day Dose-Safety Analysis Set
Placebo-Safety Analysis Set
GWP42003-P 10 mg/kg/Day Dose-Safety Analysis Set
Trial Design
2Treatment groups
Experimental Treatment
Placebo Group
Group I: GWP42003-P 10 mg/kg/dayExperimental Treatment1 Intervention
Participants will be stratified based on their age (6 to 11 years old, 12 to 17 years old), use of antipsychotics (on versus off), and region (North America versus Rest of the World) and will be randomized to receive 5 milligrams per kilogram per day (mg/kg/day) GWP42003-P for 1 week and then 10 mg/kg/day GWP42003-P for 11 weeks.
Group II: PlaceboPlacebo Group1 Intervention
Participants will be stratified based on their age (6 to 11 years old, 12 to 17 years old), use of antipsychotics (on versus off), and region (North America versus Rest of the World) and will be randomized to receive matching placebo for 12 weeks.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
GWP42003-P
2016
Completed Phase 3
~1740
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Common treatments for Autism Spectrum Disorder (ASD) include behavioral therapies, medications, and emerging treatments like Cannabidiol (CBD). CBD works by modulating the endocannabinoid system, which plays a role in regulating mood, social behavior, and neurological development.
This modulation can help reduce symptoms such as anxiety, aggression, and repetitive behaviors in ASD patients. Understanding these mechanisms is crucial as it provides insight into how CBD and similar treatments can improve the quality of life for individuals with ASD by targeting specific neurological pathways involved in the disorder.
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Who is running the clinical trial?
GW Research LtdLead Sponsor
35 Previous Clinical Trials
3,117 Total Patients Enrolled
1 Trials studying Autism Spectrum Disorder
1 Patients Enrolled for Autism Spectrum Disorder
Jazz PharmaceuticalsLead Sponsor
249 Previous Clinical Trials
34,733 Total Patients Enrolled
3 Trials studying Autism Spectrum Disorder
102 Patients Enrolled for Autism Spectrum Disorder
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- You are moderately ill according to a standard rating scale used in the study.You are at least 12 kilograms (kg) in weight.You have a diagnosis other than Autism Spectrum Disorder (ASD) that is more prominent, like Attention Deficit Hyperactivity Disorder (ADHD).You are currently taking more than two medications for epilepsy.You are currently taking clobazam.You have a known or suspected allergy to cannabinoids or any of the ingredients in the medication, like sesame oil.You have a history of attempting suicide or have had strong thoughts of wanting to harm yourself recently.You have a score of 15 or more on the ABC-I irritability subscale.You had brain surgery or a serious head injury within the past year.You are willing and able to give informed assent and consent for participation in the trial.You are willing and able (in the investigator's opinion) to comply with all trial requirements.You are currently taking sirolimus, everolimus, temsirolimus, or tacrolimus medications.You are currently taking certain medications like repaglinide, pioglitazone, rosiglitazone, montelukast, bupropion, or efavirenz.You currently have bipolar disorder, psychosis, schizophrenia, schizoaffective disorder, or major depression that is not in remission.You have a worsening neurological condition.You have had seizures within the last 24 weeks.You are currently taking omeprazole, lansoprazole, tolbutamide, or warfarin.You have another serious illness or condition that could make it risky for you to participate in the trial, could affect the trial's results, or could make it difficult for you to take part.You have been assessed as moderately ill on a scale called the Clinical Global Impressions - Improvement Scale (CGI-S).
Research Study Groups:
This trial has the following groups:- Group 1: GWP42003-P 10 mg/kg/day
- Group 2: Placebo
Awards:
This trial has 0 awards, including:Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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