Clinical Trial of Nabilone for Aggression in Adults with Intellectual and Developmental Disabilities

Phase

Condition

Sjögren-larsson Syndrome

Cerebral Palsy

Williams Syndrome

Treatment

Nabilone

Clinical Study ID

NCT05273320

135-2020

Ages 18-65
All Genders

Study Summary

Innovative treatments are urgently needed for severe behavioural problems (SBPs) in adults with intellectual and developmental disabilities (IDD). Although a synthetic cannabinoid, nabilone may be a plausible and safe alternative to treat SBP, safety and efficacy of nabilone in people with IDD has never been evaluated. The investigators propose to conduct this first-ever Phase I pre-pilot open-label clinical trial to collect data on the tolerability and safety profile of nabilone in adults with IDD, and explore changes in SBP pre- and post-treatment. The results will inform a next-stage pilot randomized controlled trial, followed by a fully powered trial eventually.

Eligibility Criteria

Inclusion

Inclusion Criteria:

Participants of any sex or gender, race or ethnicity meeting all criteria listed below will be included in the study:

Aged ≥25 years, as medical cannabis should not be used in any person aged <25 assuggested by Health Canada.
Adults with a DSM-5 diagnosis of ID meeting: a. Full scale IQ <70 on a standardizedcognitive assessment reported in their prior medical record; b. A deficit inadaptive function in at least one activity of life, as estimated by the AdaptiveBehavior Assessment System, rated by the caregiver. For those whose verified recordsare not available, they are deemed eligible if they are connected with DisabilityServices Ontario. People with ID and other developmental disabilities, e.g., autism,Down syndrome, genetic conditions such as Angelman syndrome, fragile X syndrome,Prader-Willi Syndrome, etc., will also be enrolled.
SBP, including aggressive, disruptive, and/or self-injurious behaviours in anysituation (home, day program, clinic, etc.), defined as a score ≥18 on the AberrantBehaviour Checklist-Irritability subscale (ABC-I), and a score ≥4 on the ClinicalGlobal Impressions-Severity scale. A consistent pattern of frequent SBP should occurfor >3 months ≥1 time per week.
Sexually active women of child-bearing potential must have a negative urinepregnancy test at the screening visit.
Sexually active women of child-bearing must use an effective method of birth controlat least from the start of last two normal menses before the screening visit to onemonth after the end of the study (completion of the safety visit). The acceptedmethods of contraception include total sexual abstinence, if it is the usual andpreferred lifestyle, or consistently and correctly taking the oral hormonalcontraceptive.
Adults who receive a blood test in recent 12 months, which shows liver function testwith the ALT ≤3 times the upper limit of normal and bilirubin ≤2 times the upperlimit of normal.
At least one month that needs to pass from the participation in anotherinvestigational drug trial to a given adults being allowed to participate in thistrial.

Exclusion

Exclusion Criteria:

History of hypersensitivity to any cannabinoid.
The presence of an unstable seizure disorder as defined by having not beenseizure-free for at least 3 months or anticonvulsant treatment has not been stablefor at least 4 weeks.
The presence of any clinically significant or unstable medical conditions, includingcardiovascular, liver, kidney, pulmonary disease, presence of known congenital brainmalformation, as per investigator assessment based on medical history and chartreview.
The presence of a lifetime diagnosis of psychotic disorders, bipolar disorder, orsubstance use disorder, or current diagnosis of major depressive disorder ordementia, based on past psychiatric history noted in the medical chart, as well asMoss-PAS (ID) at S-V.
Family history of psychotic disorders.
Change in psychotropic medications less than 4 weeks prior to study drug use.
At the time of screening, each adult's medication list will be checked for drugsthat are known to cause interactions with nabilone. When a given adult is taking anydrugs or is taking a given medication exceeding a given dose) in the following list,he/she/they will be excluded.
Currently on benzodiazepines at the dose more than the benzodiazepineequivalent to lorazepam 2 mg daily.
Currently on medical psychostimulant, including methylphenidate (100 mg daily),lisdexamfetamine (70 mg daily), amphetamine/dextroamphetamine (Adderall XR®, 50mg daily), dextroamphetamine (Dexedrine®, 50 mg daily) at the dose exceedingtheir respective maximum doses (as shown in the bracket after each agent) totreat ADHD in adults, based on the CADDRA guideline, www.caddra.ca.
Currently on nonbenzodiazepine hypnotics, including zaleplon (10 mg daily),zolpidem (10 mg daily), and zopiclone (7.5 mg daily), at the dose exceedingtheir respective suggested safety doses (as shown in the bracket after eachagent), based on Canadian Recalls and Safety Alerts (https://healthycanadians.gc.ca/recall-alert-rappel-avis/).
Currently on any opioids.
Currently on barbiturates.
Drinking any alcohol one week before the screening visit.
Recreational use of any psychomimetic drugs, including Ketamine, LSD, MDMA,Magic mushrooms, PCP, Salvia, GHB, Bath salts, Methamphetamine; the last usehappens within one week before the screening visit.
Adults currently taking other cannabinoids, such as CBD or medical cannabis, fromanother source, unless participants and/or their caregivers are willing to stop thistreatment for at least 4 weeks prior to entering the study.
Adults who might travel out of the area for a significant time during the study.
Adults who recently are participating in another investigational drug trial.
Pregnancy.
Sexually active women of child-bearing potential intended to give breastfeeding orto get pregnant.

Study Design

Nabilone

March 17, 2022

December 31, 2025

Study Description

Current medications for severe behavioural problems (SBP) show equivocal effectiveness and are associated with a high risk of side effects. Innovative and safe treatments are urgently needed. While preclinical studies, anecdotal reports, and uncontrolled studies link SBP with an endocannabinoid mechanism and suggest that medical cannabinoids may be an efficacious and safe alternative to current medications for SBP in adults with IDD, rigorous evidence is still in the very early stages. Unlike cannabidiol (CBD), a cannabinoid with elusive mechanisms and dose ranges, nabilone, a marketed synthetic cannabinoid, has a clearer mechanism, favourable safety profile, and more predictable dosing. Data of safety and efficacy regarding nabilone in this population has never been published.

This study is a Phase I pre-pilot open-label trial of nabilone in adults with IDD and SBP. The trial first includes a screening visit (S-V) for eligibility, then a baseline visit (V 0), followed by a dose titration phase, and then a 4-week open label phase at a stable dose. At the end of the open label phase, participants will undergo a termination visit (V 1), after which nabilone will be tapered off over 8 days. And then, 2 weeks later, participants will undergo a last follow-up visit (V-F) to ensure safety.

At S-V, and before the informed consent process, the participant will be assessed for capacity to provide informed consent. If they cannot pass the competence test using the MacArthur Competence Assessment Tool for Clinical Research (MacCAT-CR), then the written informed consent will be obtained from their substitute decision-maker after seeking participants' assent.

At S-V, participants will also be assessed for eligibility based on the inclusion and exclusion criteria, including SBP defined as a score ≥18 on the Aberrant Behaviour Checklist-Irritability subscale (ABC-I) and a score ≥4 on the Clinical Global Impressions-Severity scale. The SBP should present with a consistent pattern with the frequency of ≥1 time per week for >3 months.

At V 0 the following assessments will be completed:

Clinical Global Impression - Severity scale (CGI-S) will be rated by the investigator to evaluate the severity of the behavioural problems.
Measuring baseline vital signs and weight to monitor any AEs of nabilone.
Assessment of participants' cognitive capacity using the NIH Toolbox® Cognition Battery. Previous evidence suggests that nabilone may cause acute mild decrement in attention and working memory. The investigators will use the NIH Toolbox® Cognition Battery, which has been shown as a good candidate outcome measure to examine broad nonverbal cognitive changes for individuals with IDD (valid and reliable for those with a mental age of ≥5 years; implementable for those with a mental age of ≥3 years), to assess the baseline attention and working memory.
Assessment of SBP of participants, including behavioural problems using the ABC-I and Modified Overt Aggression Scale (MOAS), as reported by the caregivers. These scales will be the principal measures for detection of changes in SBP.
Assessment of anxiety using the parent-rated General Anxiety Subscale of the Anxiety, Depression, and Mood Scale (ADAMS). Nabilone and THC at low doses have been shown to alleviate anxiety, thus this measure is used for exploratory aims to detect a signal of behavioural/mood change with nabilone use.
Assessment of caregiver's stress and crisis using the Stress Subscale of Depression Anxiety Stress Scales (DASS-21) and Brief Family Distress Scale (BFDS). As SBP cause major caregiver burden, the investigators aim to assess whether the caregiver's stress and distress would improve if nabilone also improves participants' SBP.
Exploratory assessment of autism symptoms using the Social Communication Questionnaire for Adults with Intellectual Disability (SCQ-AID). Prior evidence suggests that autistic symptoms may be associated with the presentation of SBP. The investigators aim to explore whether the baseline autistic symptoms would modulate treatment effects of nabilone.
Optional assessment of MRI Imaging (dependent on the participant's ability to comply with the following assessments, in the opinion of the carers/parents and investigator).

After V 0, eligible participants will receive open-label nabilone starting with a dosage of 0.25 mg before sleep. During the dose titration phase (which could last up to 15 days), nabilone will be titrated in 0.25 mg increments every two days (with the dosing schedule "twice daily") after consultation with the study team during regular phone calls. The study team will also check whether the participants show any physical or mental changes which are believed to be attributed to AEs (based on the UKU side effect rating scale), and advise the participant and their caregivers on the next step of titration accordingly. Dose adjustments are performed until the participant reaches the maximum permitted dose of 1 mg twice daily or experience intolerable AEs believed to be related to nabilone. If intolerable, the participant will use nabilone at the previous lower dose, entering the open label phase.

Participants will be then on a stable, optimized nabilone dosage for four weeks, and then the trial ends with an on-site termination visit (V1). If there are any changes suspected to be associated with AEs, the UKU side effect rating scale will be assessed during the telephone check-up.

At V 1, the following post-treatment assessments will be completed:

Assessment of adverse events using the UKU side effect rating scale, examined by the researcher or investigator, to systemically investigate the physical AEs of nabilone.
Re-measuring of vital signs (including blood pressure to check orthostatic hypotension) and weight to monitor the physical AEs of nabilone.
Re-assessment of participants' cognitive capacity using the NIH Toolbox® Cognition Battery, to monitor any acute cognitive change (AEs) due to nabilone.
Re-assessment of caregiver rated ABC-I, MOAS, and General Anxiety Subscale of ADAMS. CGI-S and CGI-I will be rated by the investigator to evaluate the severity and improvement of the behavioural problems after nabilone treatment. These re-assessments are implemented to fulfil the exploratory study aim of assessing behavioural changes pre- and post-treatment of nabilone.
Re-assessment of caregiver's stress and crisis using the Stress Subscale of DASS-21 and BFDS, to investigate changes in their stress and distress after participants takes nabilone.
Optional re-assessment of MRI Imaging for those who finish the pre-treatment MRI and are willing to receive the second wave of MRI imaging. This is to investigate the change in brain function and structure pre- and post-treatment of nabilone.

Nabilone will be tapered in 0.25 mg daily decrements to prevent acute withdrawal effects. Phone calls will be held every other day during the dose-tapering phase, to check whether there are any changes which are believed to be attributed to withdrawal effects. A safety follow-up visit (S-F) will be scheduled after 2 weeks of full discontinuation from the study drug.

Connect with a study center

Centre for Addiction and Mental Health
Toronto, Ontario M6J 1H4
Canada
Active - Recruiting

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