NTI164 in Autism Spectrum Disorder

Trial statusNot yet recruiting
Trial phasePhase 3
Trial typeInterventional
Biological sexAll
Age6-21
SponsorFenix Innovation Group

About this trial

This is a double-blind, randomised, placebo-controlled study investigating the efficacy of a full-spectrum medicinal cannabis plant extract on core and associated ASD symptoms over placebo. Participants will be randomly allocated to either NTI164 or placebo at a 1:1 ratio and blood samples will be collected and surveys completed at baseline and Week 16. This study will expand efficacy and safety data of NTI164 and provide additional mechanism of action data of NTI164 in this patient cohort.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Participant is aged 6 years to 21 years (inclusive).

Participant is at a healthy weight at the discretion of the Principal Investigator.

Written informed consent from parent or legal guardian according to the local law.

Participants can comply with trial requirements.

Disqualifiers

Current diagnosis of bipolar disorder, psychosis, schizophrenia, schizoaffective disorder, or active major depression.

Has a diagnosis other than ASD that dominates the clinical presentation (e.g., ADHD).

Has a degenerative condition.

Changes in anticonvulsive therapy within the last 12 weeks.

Trial design

Design model

Parallel

Treatments tested in this trial

  • NTI164

    Drug

    A CBDA-dominant full-spectrum medicinal cannabis plant extract with extremely low THC.

  • Placebo

    Drug

    Placebo oil suspension

Treatment groups

200 Participants
are divided into 2 treatment groups
Group A: ActiveExperimental treatment 1 intervention
Group B: PlaceboPlacebo comparator 1 intervention

Trial outcomes

Primary outcomes

1

Vineland Adaptive Behaviour Scales, 3rd Edition (Vineland-3)

Used to measure functioning across 3 core domains, Communication, Daily Living Skills, and Socialisation, as well as 2 optional domains, Motor Skills and Maladaptive Behaviour. The core domains sum to a total Adaptive Behaviour Composite. Scores are between 20-160, higher scores indicate better outcomes.

Time frame
Baseline, Week 16

Secondary outcomes

1

Social Responsiveness Scale, 2nd Edition (SRS-2)

Captures overall change in core ASD symptoms across domains including social awareness, social cognition, social communication, social motivation, and restricted and repetitive behaviours. Scores are between 0-195, and higher scores indicate greater impairment.

Time frame
Baseline, Week 16
2

Clinical Global Impression - Improvement (CGI-I)

Provides a clinician-rated global assessment of improvement at a given time point following an intervention. 1-3 = improvement, 4 = no change, 5-7 = worsening.

Time frame
Baseline, Week 16
3

Clinical Global Impression - Severity (CGI-S)

Evaluates a clinician's impression of disease severity at a given time point from a scale of 1-7. A higher score indicates greater impairment/disease severity.

Time frame
Baseline, Week 16
4

Anxiety, Depression, and Mood Scale (ADAMS)

Measures emotional and behavioural disturbances frequently comorbid with ASD. Assesses 5 domains (Manic/hyperactive Behaviour, Depressed Mood, Social Avoidance, General Anxiety, and Compulsive Behaviour). Scores are between 0-84, with higher scores indicating greater impairment.

Time frame
Baseline, Week 16

Other outcomes

1

Research samples - transcriptomics

To further clarify the mechanism of action of NTI164, both bulk and single-cell RNA sequencing will be performed on peripheral blood mononuclear cells (PBMCs) from patients at specified time points. This will provide additional information regarding which genes are being expressed in patients at either abnormally low or high levels compared to a non-ASD population, and the effects NTI164 has on gene expression. This workflow includes RNA extraction, depletion of ribosomal RNA via hybrid capture, library preparation, and sequencing. Cleaned sequence reads will then be aligned against the Homo sapiens genome (Build version hg38) and STAR aligner (v2.5.3a) will be used to map unique reads to the genomic sequences. This is exploratory so genes of interest cannot be identified in advance.

Time frame
Baseline, Week 16
2

Research bloods - proteomics (and phosphoproteomics)

To further clarify the mechanism of action of NTI164, proteomics and phosphoproteomics will be performed on peripheral blood mononuclear cells (PBMCs) from patients at specified time points. This will provide additional information regarding which proteins are being expressed at either abnormally low or high levels compared to a non-ASD population, as well as how extensively these proteins are phosphorylated compared to a non-ASD population, and the effects NTI164 has on protein expression and phosphorylation. Samples will be tagged using the TMTpro system and hydrophilic ion liquid chromatography fractionation performed. This is exploratory so proteins of interest cannot be identified in advance.

Time frame
Baseline, Week 16
3

Research bloods - Methylomics

To further clarify the mechanism of action of NTI164, methylomics will be performed on whole blood from patients at specified time points. This will provide additional information on methylation patterns (e.g. addition of a methyl group to histones or DNA) in patients compared to non-patients, and how NTI164 effects this type of epigenetic modification and how genes of interest may be regulated. This is exploratory so patterns of interest cannot be identified in advance. Genome-wide methylation will be assessed using the Illumina MethylationEPIC v2.0 BeadChip (or the latest version if a new version is available to the study team at the time of analysis).

Time frame
Baseline, Week 16
4

Research bloods - cytokine assay

To further clarify the mechanism of action of NTI164, a cytokine assay investigating a panel of inflammatory markers will be performed on plasma from patients at specified time points. The cytokine assay will likely be the LEGENDplex Human Neuroinflammation Panel 1 (13 plex). Cytokines investigated with this panel include VILIP-1, CCL2, sTREM-2, b-NGF, TGF-b1, TNF-a, IL-6, s-TREM-1, sRAGE, CX3CL1, VEGF, BDNF, and IL-18.

Time frame
Baseline, Week 16

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Fenix Innovation Group

Lead sponsor

Neurotech International Limited

Collaborator

This trial is not recruiting at the moment. You can still explore other options: