CASCADE: CAnnabidiol Study in Children With Autism Spectrum DisordEr

NCT04520685 | Active Not Recruiting Phase 2 FDA Drug

• 1 other identifier: 19-2168
• Study Type: interventional
• Target: 86
• Locations: 1 country
• Sites: 1

Brief Summary

This is a randomized, placebo-controlled study but all study participants will receive the active study medication at some point during the study for at least 12 weeks, and some children with receive CBD for the entire study.

Conditions

Autism Spectrum Disorder

Keywords

CBD; cannabidiol; ASD; autism spectrum disorder; autism

Outcome Measures

Primary Outcomes (1)

• Aberrant Behavior Checklist- 2nd Edition (ABC-2): Irritability subscale raw score

  The Aberrant Behavior Checklist- 2nd Edition (ABC-2) is a standard parent/caregiver reported behavioral outcome measure for use in developmental disability clinical trials. The ABC-2 is a 58-item questionnaire and measures domains of Irritability, Lethargy/Social Withdrawal, Stereotypic Behavior, Hyperactivity/noncompliance, and Inappropriate Speech. Behaviors are assessed using a 4-point Likert scale. Scores range from "not at all a problem" (0) to "the problem is severe in degree" (3). The Irritability subscale range is from 0 to 45.

  Baseline to Week 12

Secondary Outcomes (23)

• Aberrant Behavior Checklist- 2nd Edition (ABC-2): Lethargy/Social Withdrawal subscale

  Baseline to Week 12

• Aberrant Behavior Checklist- 2nd Edition (ABC-2): Stereotypic Behavior subscale

  Baseline to Week 12

• Aberrant Behavior Checklist- 2nd Edition (ABC-2): Inappropriate Speech subscale

  Baseline to Week 12

• Aberrant Behavior Checklist- 2nd Edition (ABC-2): Hyperactivity/Noncompliance subscale

  Baseline to Week 12

• Anxiety, Depression, and Mood Scale (ADAMS): Total Score

  Baseline to Week 12

Other Outcomes (4)

• AutismEyes Eyetracking system Autism Symptoms Index (ASI)

  Baseline to Week 12

• Telehealth Functional Behavior Analysis (Tele-FBA)

  Baseline to Week 12

• Autism Screening Instrument for Educational Planning- 3rd Edition Sample of Vocal Behavior (ASIEP-3 SVB) Vocalization Score

  Baseline to Week 12

Study Arms (3)

Arm 1: 12 weeks of study drug then 15 weeks of placebo

EXPERIMENTAL

Subjects in this group will receive cannabidiol for the first 12 weeks of the study and placebo for the last 15 weeks.

Drug: Oral cannabidiol 100mg/mL; Drug: Placebo

Arm 3: 15 weeks of placebo then 12 weeks of study drug

EXPERIMENTAL

Subjects in this group will receive placebo for the first 15 weeks of the study and cannabidiol for the last 12 weeks.

Drug: Oral cannabidiol 100mg/mL; Drug: Placebo

Arm 3: 27 weeks of study drug

EXPERIMENTAL

Subjects in this group will receive cannabidiol throughout the entire 27 weeks of treatment.

Drug: Oral cannabidiol 100mg/mL

Interventions

Oral cannabidiol 100mg/mL DRUG

In Arm 1, patients will begin CBD in period 1 and receive placebo in period 2. In Arm 2, patients will begin placebo in period 1 and receive CBD in period 2. In Arm 3, patients will receive CBD for the entire 27 week study duration without washout. Each study period is 12 weeks and dose will be titrated up for 1 week at the beginning of a treatment period and titrated down for 1 week at the end of a treatment period, with a two week placebo washout between periods for Arms 1 and 2. The titration dose will be 5mg/kg/day and the treatment dose will be 10mg/kg/day.

Arm 1: 12 weeks of study drug then 15 weeks of placebo; Arm 3: 15 weeks of placebo then 12 weeks of study drug; Arm 3: 27 weeks of study drug

Placebo DRUG

In Arm 1, patients will begin CBD in period 1 and receive placebo in period 2. In Arm 2, patients will begin placebo in period 1 and receive CBD in period 2. In Arm 3, patients will receive CBD for the entire 27 week study duration without washout. Each study period is 12 weeks and dose will be titrated up for 1 week at the beginning of a treatment period and titrated down for 1 week at the end of a treatment period, with a two week placebo washout between periods for Arms 1 and 2. The titration dose will be 5mg/kg/day and the treatment dose will be 10mg/kg/day.

Arm 1: 12 weeks of study drug then 15 weeks of placebo; Arm 3: 15 weeks of placebo then 12 weeks of study drug

Eligibility Criteria

• Age: 5 Years - 17 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Child (0-17)

You may qualify if:

• Male or female children and adolescents aged 5-17 years, inclusive, at the time of screening.
• Judged by the investigator to be in good health at screening based upon the results of a medical history, physical examination, 12-lead ECG, and clinical laboratory test results.
• Patients must have a previous documented diagnosis of ASD by a medical or psychological professional.
• Patients must be assessed by the Investigator as being moderately to severely impacted due to ASD
• Patients who are taking psychotropic medication(s) should be on a stable regimen of no more than 2 medications for at least 4 weeks preceding study Screening and must maintain that regimen throughout the study. Psychotropic medications include (but are not limited to) antipsychotics, antidepressants, mood stabilizers, anxiolytics, and ADHD medications.
• Patients with a history of seizure disorders must currently be receiving treatment with a stable regimen of one or two AEDs, or must be seizure-free for 1 year if not currently receiving AEDs.
• Patients with seizures should be on a stable regimen for the 3 months preceding study enrollment of no more than 2 of the permitted anti-epileptic drugs (AEDs). Patients must remain on a stable AED dose throughout the study.
• If patients are receiving non-pharmacological educational, behavioral, and/or dietary interventions or therapies, they must be stable and have been doing so for 2 months prior to screening. Changes with school breaks are expected and do not apply.
• Patients must have a BMI of between 12-32 kg/m2 (inclusive).
• Females of childbearing potential and must have a negative serum pregnancy test at the Screening Visit and a negative urine pregnancy test at all designated visits.
• Patients/caregivers agree to abide by all study restrictions and comply with all study procedures.
• Parents/caregivers must be able to read and respond to questions and questionnaires in English.
• Patients/caregivers must be adequately informed of the nature and risks of the study and give written informed consent prior to screening.
• Parents/caregiver(s) must provide written consent to assist in study drug administration.
• In the Investigator's opinion, patients/caregivers are reliable and willing and able to comply with all protocol requirements and procedures (including scheduled visits and confinement periods).

You may not qualify if:

• Adolescent females who are pregnant, nursing, or planning a pregnancy. Females of childbearing potential and male patients with a partner of childbearing potential who are unwilling or unable to use standard acceptable methods of contraception (including abstinence, hormonal contraception, diaphragm, cervical cap, vaginal sponge, condom, or intrauterine device) for the duration of the study and for 1 month after the last dose of study medication.
• History of significant allergic condition, significant drug-related hypersensitivity, or allergic reaction to any compound or chemical class related to CBD (Epidiolex) or its ingredients.
• Exposure to any investigational drug or device \< 30 days prior to screening, or plans to take another investigational drug at any time during the study.
• Use of any THC or CBD-containing product within 4 weeks of Screening Visit, planned use during the study, or positive THC urine test at screening.
• Patient is using the following medications: clobazam (Onfi, Frisium), felbamate (Felbatol), vigabatrin (Sabril), or everolimus (Afinitor).
• Plan to initiate or change pharmacologic or non-pharmacologic interventions during the course of the study.
• Patient has ALT, AST, total bilirubin, or creatinine levels ≥ 2 times the ULN, alkaline phosphatase levels ≥ 3 times the ULN, or Hct \<1.2 times the LLN as determined from screening safety laboratories.
• Severe or unstable symptoms of ASD that may interfere with the study outcome evaluations and interpretation of results.
• Suffering from acute or progressive neurological disease, psychosis, schizophrenia or any psychiatric disorder or severe psychiatric abnormalities that are likely to require changes in drug therapy or interfere with the objectives of the study or the ability to adhere to protocol requirements.
• Has suspected or confirmed cardiovascular disease.
• History of treatment for, or evidence of, drug or alcohol abuse within the past year.

Sponsors & Collaborators

• University of Colorado, Denver: lead

Study Sites (1)

Children's Hospital Colorado

Aurora, Colorado, 80045, United States

Location

Related Publications (2)

• Sannar EM, Winter J, Franke RK, Werner E, Rochowiak R, Romani PW, Miller OS, Semmler N, Bainbridge JL, Natvig C, Mikulich-Gilbertson SK, Tartaglia NR. Cannabidiol for treatment of irritability and aggressive behavior in children and adolescents with autism spectrum disorder: background and methods of the cannabidiol study in children with autism spectrum disorder study. Int J Clin Trials. 2025 Jan-Mar;12(1):29-37. doi: 10.18203/2349-3259.ijct20250131. Epub 2025 Jan 28.

  PMID: 41103807 DERIVED

• Iffland M, Livingstone N, Jorgensen M, Hazell P, Gillies D. Pharmacological intervention for irritability, aggression, and self-injury in autism spectrum disorder (ASD). Cochrane Database Syst Rev. 2023 Oct 9;10(10):CD011769. doi: 10.1002/14651858.CD011769.pub2.

  PMID: 37811711 DERIVED

MeSH Terms

Conditions

Autism Spectrum Disorder; Autistic Disorder

Interventions

Cannabidiol

Condition Hierarchy (Ancestors)

Child Development Disorders, Pervasive; Neurodevelopmental Disorders; Mental Disorders

Intervention Hierarchy (Ancestors)

Cannabinoids; Terpenes; Hydrocarbons; Organic Chemicals

Study Design

• Study Type: interventional
• Phase: phase 2
• Allocation: RANDOMIZED
• Masking: TRIPLE
• Who Masked: PARTICIPANT, CARE PROVIDER, INVESTIGATOR
• Purpose: TREATMENT
• Intervention Model: CROSSOVER
• Sponsor Type: OTHER
• Responsible Party: SPONSOR

Model Details: For this study, participants will be randomly assigned to one of the following groups: 1. Group A will receive cannabidiol for the first 12 weeks of the study and placebo for the last 15 weeks. 2. Group B will receive placebo for the first 15 weeks of the study and cannabidiol for the last 12 weeks 3. Group C will receive cannabidiol throughout the entire 27 weeks of treatment

Study Record Dates

• First Submitted: July 29, 2020
• First Posted: August 20, 2020
• Study Start: December 15, 2021
• Primary Completion: January 31, 2024
• Study Completion: December 31, 2024
• Last Updated: May 8, 2024

Record last verified: 2024-05

Locations

US (1)