The Safety and Efficacy of Terpene-enriched Cannabidiol (CBD) Oil in ADHD

Bazelet Nehushtan LtD.

Status and phase: Enrolling; Phase 2

Conditions: Attention Deficit Hyperactivity Disorder (ADHD)

Treatments: Drug: Oral Placebo; Drug: Oral CBD oil enriched with terpenes

Study type: Interventional

Funder types: Industry

Identifiers

NCT06542445

ASF-0243-22

Details and patient eligibility

About

ADHD is the most frequent neurodevelopmental disorder in childhood. Symptoms often appear in preschool years, and most children (65-80%) continue to experience some ADHD-associated symptoms into adolescence and adulthood. The disorder is marked by age-inappropriate inattention, hyperactivity, and impulsivity. Drug treatments for ADHD include stimulants containing methylphenidate (like Ritalin and Concerta) or amphetamines (like Vyvanse). However, 30-35% of the patients do not respond well to these treatments, and stimulants may result with various side effects.

The use of medical cannabis increases; applied for expending medical conditions, with growing evidence for its beneficial effects. A study on ADHD adults treated by cannabinoids demonstrated improvements in hyperactivity and impulsivity.

The current study is aimed to examine the safety and efficacy of treating children diagnosed with ADHD with a CBD oil (devoid of THC), enriched with terpenes. Participants will be randomly assigned to receive either the enriched CBD oil or a placebo, for 5 weeks (Treatment, Stage I).

At the end of the treatment stage (I), an open-label stage will follow (II), wherein, all participants will receive the investigational product for an additional 5 weeks.

The investigators hypothesize that children treated with the enriched CBD oil (Treatment, Stage I) will show significantly higher improvement in hyperactivity and inattention scores, as compared with the placebo group.

Full description

Screening phase:

Parents who are interested to take part in study, will contact the study team. Parents will be asked to provide documents attesting their child's medical status and forms required to process a medical cannabis prescription.

Visit 1 - Baseline:

• Participants and parents will sign an Informed Consent Form.
• Parents will complete questionnaires about the child's health, clinical history, medications, sleep, eating habits, and quality of life.
• Participants will be examined by a pediatrician, who will fill out a physical examination report, including height, weight and blood pressure, and will conduct an urine test.
• Participants will conduct a TOVA (Test of Variables of Attention) test, and answer a CBCL (Child Behavior Checklist) questionnaire.
• Parents and teachers will complete the Conners questionnaires (sent during the screening phase. Conners questionnaires may be filled out prior to Visit 1, but no longer than two weeks prior to Visit 1).
• Participants and parents will receive the study drug/placebo and usage instructions.

Treatment using the study drug (Stage I) will be initiated following Visit 1, according to a schedule set by the study team.

Follow-up 1:

The study team will contact the parents via a phone call two weeks (±2 days) after initiation of stage I. Parents will answer questions regarding general health and side effects.

Visit 2 -at the end of Stage I:

• Five weeks (±3 days) after initiation of stage I.
• Participants and parents will undergo and fill out the same set of examinations and questionnaires as in Visit 1.
• All participants will receive new bottles of the investigational product - the CBD oil enriched with terpenes (open label, Stage II).

Follow-up 2:

• The study team will contact the parents via a phone call two weeks (±2 days) after initiation of Stage II. Parents will answer questions regarding general health and side effects.

Visit 3 - at the end of Stage II:

• Five weeks (±3 days) after initiation of stage II.
• Participants and parents will undergo and fill out the same set of examinations and questionnaires as in Visit 1, excluding the TOVA test.
• Study drugs' bottles and cannabis use prescription will be returned to the study team.

Enrollment: 120 estimated patients

Sex: All

Ages: 6 to 18 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

1. Children/adolescents aged 6-18 diagnosed with ADHD as per DSM-V by a neurologist, psychiatrist or other specialist.
2. Willing/able to arrive to all the necessary visits as per study protocol.

Exclusion criteria

1. Participants who used ADHD conventional medications in the month before starting the study or intend to do so during the study.
2. Participants who used benzodiazepines or first-generation antihistamines in the week before starting the study or other drugs which may interfere with the study as per PI opinion.
3. Participants suffering from neurological or psychiatric diseases.
4. Participants suffering from neoplastic diseases.
5. Participants with syndromes or metabolic diseases.
6. Participants with a significant clinic diagnosis which may interfere with the study. May be included later on as per PI opinion.
7. Pregnant or breastfeeding adolescents.
8. Sexually active female adolescents who are unwilling to use contraceptives.
9. Participants that in the PI opinion will not comply with the protocol in a way that will harm the study (for ex.: not using contraceptives.)
10. Participants with less than 18 kg or more than 90 kg weight.
11. Participants with BMI lower than 18 or higher than 29.9.
12. Participants engaged in another clinical study which includes a medicine.
13. Participants engaged in another study regarding ADHD treatment of any kind.
14. Participants using alcohol or drugs.
15. Past or present use of Cannabis, including medical cannabis

Criteria for early termination:

1. Use of another medication for ADHD during the study.
2. Use of a medication from the exclusion criteria list during the study.
3. Use of alcohol or drugs during the study.
4. Participants who got pregnant during the study.
5. Participants who split the first visit and did not arrive to the second part of the first visit after a maximum of 28 days.
6. Participants who did not start the treatment during the 14 days from receiving the drug.
7. Non -compliant participants.

Criteria for exchange:

1. PI may exchange participants that quit, if they did not start treatment for new participants.
2. PI may recruit again participants who quit after a new full recruitment process.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Quadruple Blind

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120 participants in 2 patient groups, including a placebo group

CBD oil enriched with terpenes

Active Comparator group

Description:

24% CBD, terpenes, MCT oil.

Treatment:

Drug: Oral CBD oil enriched with terpenes

Placebo oil

Placebo Comparator group

Description:

fragrances and flavors, MCT oil.

Treatment:

Drug: Oral Placebo