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Completed

NCT Number: NCT03594552

Modulation of the Brain Excitatory/Inhibitory (E/I) Balance in Autism Spectrum Disorder (ASD)

This study investigates the brain response to a single acute dose of Arbaclofen, the R-enantiomer of the GABA-B agonist Baclofen, compared to a single dose of placebo in healthy men with and without autism spectrum disorder.

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Key information

Age range

18 year–60 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

King's College London

London, SE5 8AF, United Kingdom

About this study

Previous research suggests that GABAergic drug compounds could shift brain excitation and inhibition (E-I) in the healthy brain and in neurodevelopmental psychiatric conditions, such as autism spectrum disorder (ASD) - where this balance is disrupted. A study by Ajram et al. (2017) has shown an E-I shifted towards more GABA in individuals with ASD, and not in controls, after a single dose of the anti-glutamatergic and pro-GABAergic drug Riluzole. Moreover, brain connectivity patterns in ASD patients where shifted towards the ones observed in the control group. However, it was unclear whether this changes could be driven by GABA receptors, thus more specific probes may help to clarify the mechanism underlying the E-I coordination in ASD. Therefore, this study will use neuroimaging and electrophysiology to investigate the brain E-I coordination in ASD compared to control participants when the system is responding to a single dose of the specific GABA-B (STX209) receptor agonist. 50 adult individuals with ASD and 50 neurotypical adults (25 males and 25 females per group) will be invited to participate. Each participant will receive a single dose of the drug (15mg or 30mg Arbaclofen) or matched placebo). Brain activity and neurochemistry will be investigated using magnetic resonance imaging. Further data will be collected through questionnaires, behavioural tasks, blood samples, and sensory tasks using electroencephalography and retinal imaging.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • ASD participants must pass diagnostic threshold for ASD on the Autism Diagnostic Interview-Revised (if and informant is available)
  • ASD participants must be currently symptomatic on Autism Diagnostic Observation Schedule (ADOS)
  • Age 18-60 years
  • Can give informed consent
  • medication free in the month preceding participation; but regular medication (used in a stable dose over the two months previous to participation) with drug which does not affect glutamate or GABA directly may be permitted
  • IQ>70

Exclusion criteria

  • IQ<70
  • history of psychosis, co-morbid major mental illness, significant physical illness (heart disease, high blood pressure, seizures) habitual substance misuse (including alcohol)
  • ASD caused by a known genetic syndrome e.g. Fragile X or 22q11 deletion syndrome,
  • past/present treatment for epilepsy
  • Change of medication dose/start of a new pharmacological therapy in the month prior to participation

Treatment and study plan

Arbaclofen_15

Drug

Single oral dose (15mg)

Other names: r-baclofen, STX209

Arbaclofen_30

Drug

Single oral dose (30mg)

Other names: r-baclofen, STX209

Placebo

Drug

Single oral dose placebo (oral tablet)

Other names: Placebo oral tablet

Primary outcomes

  1. Neurochemical response to GABAergic stimulation.

    Time frame: Through study completion, an average of 2 years.

    Comparing brain excitation-inhibition measures (i.e., glutamate and GABA) when the GABAergic system is activated by a single oral dose of the GABA-B drug Arbaclofen versus the placebo condition.

Secondary outcomes

  1. Functional connectivity measures using resting state functional magnetic resonance imaging.

    Time frame: Through study completion, an average of 2 years.

    Maps of functional connectivity will be obtained for each condition and compared between adults with and without ASD.

  2. Brain oscillations under sensory stimulation

    Time frame: Through study completion, an average of 2 years.

    Brain oscillations and event-related potentials will be recorded during sensory stimulation using high density electroencephalography.

Sponsors and collaborators

Lead sponsor

King's College London

Other

Registry information

Official study title

Modulation of the Brain Excitatory/Inhibitory (E/I) Balance Through Neuronal and Glial Systems in Autism Spectrum Disorder (ASD

Important dates

Study start
2018
Primary completion
2020
Study completion
2020
First posted
Jul 20, 2018
Registry last updated
Nov 22, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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