Low-THC cannabis extract improves autism symptoms in trial

NTI164, a novel medicinal cannabis extract, improves core symptoms of autism spectrum disorder: Results from a double-blind, randomised, controlled trial (The Harmony study).

Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics • • Highly Relevant
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AI Summary

A double-blind, randomised, placebo-controlled Phase II/III clinical trial tested NTI164, a full-spectrum medicinal cannabis extract containing less than 0.3% THC, in children with Level II/III autism spectrum disorder (ASD). Participants received NTI164 or placebo for 8 weeks, with some later receiving NTI164 in an open-label phase. The abstract reports an excellent safety profile but does not provide numerical effect sizes or participant numbers.

Compared with placebo, NTI164 was associated with statistically significant improvements in overall clinical severity, adaptive functioning, social responsiveness, and affective symptoms. Caregivers also reported better family experiences and quality of life. These findings suggest that this low-THC cannabis product may warrant further study as a potential treatment for core and associated ASD symptoms, although the results do not establish that all cannabis products—or THC generally—will have the same effects.

💡 Key Findings

1
NTI164 showed an excellent safety profile in this paediatric clinical trial.
High
80%
2
Compared with placebo, NTI164 produced statistically significant improvements in overall clinical severity, adaptive functioning, social responsiveness, and affective symptoms.
High
85%
3
Caregivers reported improved family experiences and quality of life during NTI164 treatment.
Good
75%
4
The abstract reports benefits in both the double-blind and open-label phases, supporting further clinical development of NTI164 for autism spectrum disorder.
High
80%

📄 Original Abstract

Autism spectrum disorder (ASD) is a heterogeneous neurodevelopmental disorder, characterised by difficulties with communication, social interaction, repetitive behaviours, restricted interests, and varying levels of intellectual disability. Aetiology remains unclear for many patients and the underlying physiology is complex. Approved pharmacological treatments of ASD target irritability, temper tantrums, and agitation, with no therapies targeting core ASD symptoms. This double-blind, randomised, placebo-controlled Phase II/III clinical trial investigated the efficacy and safety of NTI164, a novel full-spectrum medicinal cannabis product with <0.3% tetrahydrocannabinol (THC), in paediatric patients with Level II/III ASD. Participants were recruited from a tertiary paediatric neurology clinic and randomised to receive NTI164 up to 20 mg/kg/day or placebo for an 8-week double-blind phase; participants receiving placebo were able to receive NTI164 in an 8-week open label phase following the double-blind phase. Safety assessments, clinician-, and caregiver-rated tools measuring symptoms were utilised at baseline and Week 8. Analysis of Covariance (ANCOVA) was used for statistical analyses. NTI164 demonstrated an excellent safety profile, and statistically significant and meaningful improvements compared to placebo in overall clinical severity, adaptive functioning, social responsiveness, and affective symptoms. Caregivers also reported improved family experiences and quality of life with NTI164. Participants who transitioned from placebo to NTI164 open label reported similar improvements as those reported during the double-blind phase. NTI164 significantly improved core and associated symptoms of ASD compared to placebo. Consistent benefits reported by both clinicians and caregivers in both open label and double-blind contexts supports further clinical development of NTI164 in ASD.

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