Skip to content

Orexin Receptor Antagonists as Modulators of Threat Sensitivity in Individuals With Alcohol Use Disorder

Orexin Receptor Antagonists as Modulators of Threat Sensitivity in Individuals With Alcohol Use Disorder

Status
Completed
Phases
Early Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05656534
Enrollment
81
Registered
2022-12-19
Start date
2022-11-29
Completion date
2024-08-01
Last updated
2025-10-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Alcohol Use Disorder

Keywords

suvorexant, alcohol use disorder, electromyography, functional magnetic resonance imaging

Brief summary

The goal of this double-blind clinical trial is to further explore if, how, and for whom orexin antagonism modifies brain-behavior stress targets in moderate to severe alcohol use disorder (AUD). The main questions it aims to answer are: * Does an acute dose of suvorexant (SUV) and/or daily use of SUV modify brain-behavior targets of AUD dysfunction? * Does daily SUV use change alcohol behavior and if so, is this change in behavior linked to brain-behavior change? Participants will be randomized to a treatment group (SUV or placebo) and protocol arm, electromyography (EMG) only or EMG+functional magnetic resonance imaging (fMRI). Participants will be asked to complete the following: * Baseline lab visit(s) that include the psychophysiological stress paradigm (EMG only or EMG+fMRI, dependent upon randomization). * Acute drug challenge where the participant will return to the lab to repeat the stress paradigm following administration of a single dose of either 10mg SUV or placebo. * Medication trial where participants will be instructed to take 10mg capsules of SUV or placebo orally each night before bedtime for 4-weeks. * Daily reports of medication adherence, side-effects, sleep, alcohol use, and mood will be collected via smartphones during the 4-week medication trial. * Post-treatment lab visit(s) where participants will return to the lab at the end of the medication trial and complete the same stress paradigm from baseline (EMG only or EMG+fMRI, dependent upon randomization).

Interventions

DRUGSuvorexant

This study is a double-blind study. Participants will complete an initial screening visit and pre-treatment lab visits (EMG, fMRI). Suvorexant (SUV) will be placed in opaque capsules with dextrose filler. After the pre-treatment visits participants will take one pill of SUV at the Acute Drug Challenge under medical supervision. Ninety minutes post ingestion participants will complete an EMG. Laboratory assessments will occur during peak concentration, 2 hours post-ingestion. At the end of the visit, participants will be given a blister pack with 28 pills. Participants will be instructed to take one pill orally about 30 minutes prior to sleep time each night for 28 days. Participants will be provided education about common side effects. Participants will complete daily surveys to monitor side effects and potential drug-drug interactions. At the end of the 28 days, participants will complete post-treatment lab visits.

OTHERPlacebo

This study is a double-blind study. Participants will complete an initial screening visit and pre-treatment lab visits (EMG, fMRI). The placebo pill will be identical in appearance to suvorexant but will contain only dextrose. Following the pre-treatment visits, participants will take one pill at the Acute Drug Challenge under medical supervision. Ninety minutes post ingestion participants will complete the EMG paradigm. At the end of the visit participants will be provided a blister pack with 28 pills. Participants will be instructed to take one pill orally about 30 minutes prior to sleep time each night for 28 days. Participants will be provided education about common side effects. Participants will complete daily surveys to monitor side. At the end of the 28 days, participants will complete post-treatment lab visits.

Sponsors

National Institute on Alcohol Abuse and Alcoholism (NIAAA)
CollaboratorNIH
Ohio State University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Age 18-65. * Participant is able to give informed consent. * Generally medically and physically healthy as confirmed by medical history. * Meet DSM-5 diagnostic criteria for current moderate or severe AUD. * Engage in heavy alcohol use defined as drinking equal or greater than 14 standard drinks per week if male and equal or greater than 7 standard drinks per week if female.

Exclusion criteria

* Clinically significant medical or neurological condition (e.g., liver disease, narcolepsy, complex sleep behaviors, severe hepatic impairment, COPD, severe obstructive sleep apnea). * Current cognitive dysfunction (traumatic brain injury, mental retardation, organic mental syndrome, pervasive developmental disorder, or dementia). * Current use of antihistamines, strong or moderate inhibitors of CYP3A liver enzymes, strong CYP3A inducers, or digoxin. * Current or past DSM-5 diagnosis of mania, schizophrenia, psychosis, suicidality, major depressive disorder, or obsessive compulsive disorder. * Current substance use disorder other than alcohol or mild cannabis use disorder. * Treatment seeking for AUD. * Recent psychotropic medication use in the past 2 months. * Currently smokes 5 or more cigarettes (or electronic equivalent) per day. * BMI equal or greater than 35. * Engage in night-shift work. * Lack of fluency in English. * Presence of ferrous-containing metal in the body. * Inability to tolerate small, enclosed spaces. * Deafness in one or both ears. * Currently pregnant (positive pregnancy test), lactating, or not agreeing to use birth control methods during the duration of the trial.

Design outcomes

Primary

MeasureTime frameDescription
Startle Eyeblink Electromyographic (EMG) Response to Stress With an Acute Dose of SuvorexantChange from baseline to 2 hours post-ingestion of an acute dose of suvorexant.Startle EMG responses were collected during the well-validated No-Predictable-Unpredictable threat paradigm. The task includes within-subjects conditions and raw EMG responses were averaged for each condition. To quantify the difference between threat and no-threat periods, we calculated a standardized residual score for unpredictable threat (U-threat) by saving the variance leftover (i.e., the amount of variability in a dependent variable \[DV\] that is not explained by an independent variable \[IV\]) in a simple linear regression, where the no-threat EMG startle average (IV) was entered to predict the U-threat EMG startle average (DV). The U-threat residual score was used as the primary variable. It has a mean of zero and higher scores reflect greater startle reactivity to U-threat. U-threat residual scores were calculated for the baseline session and the acute challenge.
Startle Eyeblink Electromyographic (EMG) Response to Stress With Daily Use of Suvorexant.Change from baseline to post-treatment, up to 2 months.Startle EMG responses were collected during the well-validated No-Predictable-Unpredictable threat paradigm. The task includes within-subjects conditions and raw EMG responses were averaged for each condition. To quantify the difference between threat and no-threat periods, we calculated a standardized residual score for unpredictable threat (U-threat) by saving the variance leftover (i.e., the amount of variability in a dependent variable \[DV\] that is not explained by an independent variable \[IV\]) in a simple linear regression, where the no-threat EMG startle average (IV) was entered to predict the U-threat EMG startle average (DV). The U-threat residual score was used as the primary variable. It has a mean of zero and higher scores reflect greater startle reactivity to U-threat.
Percentage of Heavy Drinking Days During Daily Use of Suvorexant.Change from baseline to post-treatment, over the course of 4 weeks.Percentage of heavy drinking days (PHDD) was calculated each week for all four weeks of the trial. A heavy drinking day was defined using NIH criteria: 5+ drinks for males and 4+ drinks for females in a single day. We conducted a multilevel mixed model with PHDD from week 1 to 4 as the within-subjects variable and treatment arm as the between subjects variable.

Secondary

MeasureTime frameDescription
Changes in Neural Activation During Unpredictable Stress Anticipation Following Daily Use of Suvorexant.Change from baseline to post-treatment, up to 2 months.Activation parameter estimates (arbitrary units) were extracted from anatomical bilateral aINS masks for each individual, pre and post treatment. Specifically, activation parameter estimates were extracted from anticipation of unpredictable threat \> anticipation of no-threat individual contrast maps for each scanning session. Greater values reflect greater activation in the bilateral insula during the anticipation of unpredictable threat. A repeated measures analysis of variance was used to test the session (time 1 vs. time 2) by treatment arm interaction on bilateral aINS activation during unpredictable threat. Significance was set at p \<.05

Countries

United States

Participant flow

Recruitment details

Participants were recruited via print advertisements, word-of-mouth referrals, and internet postings throughout Columbus and the surrounding area between November 2022 and June 2024. The first participant was enrolled on November 29th, 2022 and the last participant was enrolled in June 2024.

Pre-assignment details

Of 81 enrolled participants, 64 participants were randomized to treatment.

Participants by arm

ArmCount
Placebo + EMG Only
Individuals will take a placebo pill during the Acute Drug Challenge and daily for 28 days. Placebo: This study is a double-blind study. Participants will complete an initial screening visit and pre-treatment lab visits (EMG only). The placebo pill will be identical in appearance to suvorexant but will contain only dextrose. Following the pre-treatment visits, participants will take one pill at the Acute Drug Challenge under medical supervision. Ninety minutes post ingestion participants will complete the EMG paradigm. At the end of the visit participants will be provided a blister pack with 28 pills. Participants will be instructed to take one pill orally about 30 minutes prior to sleep time each night for 28 days. Participants will be provided education about common side effects. Participants will complete daily surveys to monitor side. At the end of the 28 days, participants will complete post-treatment lab visits.
18
Suvorexant + EMG Only
Individuals will take 10mg of suvorexant (Merck & Co Inc.) during the Acute Drug Challenge and daily for 28 days. Suvorexant: This study is a double-blind study. Participants will complete an initial screening visit and pre-treatment lab visits (EMG only). Suvorexant (SUV) will be placed in opaque capsules with dextrose filler. After the pre-treatment visits participants will take one pill of SUV at the Acute Drug Challenge under medical supervision. Ninety minutes post ingestion participants will complete an EMG. Laboratory assessments will occur during peak concentration, 2 hours post-ingestion. At the end of the visit, participants will be given a blister pack with 28 pills. Participants will be instructed to take one pill orally about 30 minutes prior to sleep time each night for 28 days. Participants will be provided education about common side effects. Participants will complete daily surveys to monitor side effects and potential drug-drug interactions. At the end of the 28 days, participants will complete post-treatment lab visits.
18
Placebo+fMRI+EMG
Individuals will take a placebo pill during the Acute Drug Challenge and daily for 28 days. Placebo: This study is a double-blind study. Participants will complete an initial screening visit and pre-treatment lab visits (EMG, fMRI). The placebo pill will be identical in appearance to suvorexant but will contain only dextrose. Following the pre-treatment visits, participants will take one pill at the Acute Drug Challenge under medical supervision. Ninety minutes post ingestion participants will complete the EMG paradigm. At the end of the visit participants will be provided a blister pack with 28 pills. Participants will be instructed to take one pill orally about 30 minutes prior to sleep time each night for 28 days. Participants will be provided education about common side effects. Participants will complete daily surveys to monitor side. At the end of the 28 days, participants will complete post-treatment lab visits.
15
Suvorexant+fMRI+EMG
Individuals will take 10mg of suvorexant (Merck & Co Inc.) during the Acute Drug Challenge and daily for 28 days. Suvorexant: This study is a double-blind study. Participants will complete an initial screening visit and pre-treatment lab visits (EMG, fMRI). Suvorexant (SUV) will be placed in opaque capsules with dextrose filler. After the pre-treatment visits participants will take one pill of SUV at the Acute Drug Challenge under medical supervision. Ninety minutes post ingestion participants will complete an EMG. Laboratory assessments will occur during peak concentration, 2 hours post-ingestion. At the end of the visit, participants will be given a blister pack with 28 pills. Participants will be instructed to take one pill orally about 30 minutes prior to sleep time each night for 28 days. Participants will be provided education about common side effects. Participants will complete daily surveys to monitor side effects and potential drug-drug interactions. At the end of the 28 days, participants will complete post-treatment lab visits.
13
Total64

Withdrawals & dropouts

PeriodReasonFG000FG001FG002FG003
Overall StudyPhysician Decision1100
Overall StudyWithdrawal by Subject1100

Baseline characteristics

CharacteristicPlacebo + EMG OnlySuvorexant + EMG OnlyPlacebo+fMRI+EMGSuvorexant+fMRI+EMGTotal
Age, Categorical
<=18 years
0 Participants0 Participants0 Participants0 Participants0 Participants
Age, Categorical
>=65 years
0 Participants0 Participants0 Participants0 Participants0 Participants
Age, Categorical
Between 18 and 65 years
18 Participants18 Participants15 Participants13 Participants64 Participants
Ethnicity (NIH/OMB)
Hispanic or Latino
1 Participants3 Participants0 Participants2 Participants6 Participants
Ethnicity (NIH/OMB)
Not Hispanic or Latino
17 Participants15 Participants15 Participants11 Participants58 Participants
Ethnicity (NIH/OMB)
Unknown or Not Reported
0 Participants0 Participants0 Participants0 Participants0 Participants
Race (NIH/OMB)
American Indian or Alaska Native
0 Participants0 Participants0 Participants0 Participants0 Participants
Race (NIH/OMB)
Asian
0 Participants0 Participants0 Participants0 Participants0 Participants
Race (NIH/OMB)
Black or African American
0 Participants2 Participants0 Participants1 Participants3 Participants
Race (NIH/OMB)
More than one race
0 Participants1 Participants0 Participants0 Participants1 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
0 Participants0 Participants0 Participants0 Participants0 Participants
Race (NIH/OMB)
Unknown or Not Reported
0 Participants2 Participants0 Participants0 Participants2 Participants
Race (NIH/OMB)
White
18 Participants13 Participants15 Participants12 Participants58 Participants
Sex: Female, Male
Female
10 Participants10 Participants9 Participants8 Participants37 Participants
Sex: Female, Male
Male
8 Participants8 Participants6 Participants5 Participants27 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
EG002
affected / at risk
EG003
affected / at risk
deaths
Total, all-cause mortality
0 / 180 / 180 / 150 / 13
other
Total, other adverse events
3 / 183 / 183 / 154 / 13
serious
Total, serious adverse events
0 / 180 / 180 / 150 / 13

Outcome results

Primary

Percentage of Heavy Drinking Days During Daily Use of Suvorexant.

Percentage of heavy drinking days (PHDD) was calculated each week for all four weeks of the trial. A heavy drinking day was defined using NIH criteria: 5+ drinks for males and 4+ drinks for females in a single day. We conducted a multilevel mixed model with PHDD from week 1 to 4 as the within-subjects variable and treatment arm as the between subjects variable.

Time frame: Change from baseline to post-treatment, over the course of 4 weeks.

Population: All 64 participants randomized to treatment were analyzed.

ArmMeasureGroupValue (MEAN)Dispersion
ControlPercentage of Heavy Drinking Days During Daily Use of Suvorexant.Week 1 PHDD27.7 percentage of heavy drinking daysStandard Error 4
ControlPercentage of Heavy Drinking Days During Daily Use of Suvorexant.Week 2 PHDD31.2 percentage of heavy drinking daysStandard Error 3.6
ControlPercentage of Heavy Drinking Days During Daily Use of Suvorexant.Week 3 PHDD27.2 percentage of heavy drinking daysStandard Error 4.2
ControlPercentage of Heavy Drinking Days During Daily Use of Suvorexant.Week 4 PHDD27.6 percentage of heavy drinking daysStandard Error 3.3
Suvorexant TreatmentPercentage of Heavy Drinking Days During Daily Use of Suvorexant.Week 4 PHDD16.9 percentage of heavy drinking daysStandard Error 2.6
Suvorexant TreatmentPercentage of Heavy Drinking Days During Daily Use of Suvorexant.Week 1 PHDD29.5 percentage of heavy drinking daysStandard Error 3.6
Suvorexant TreatmentPercentage of Heavy Drinking Days During Daily Use of Suvorexant.Week 3 PHDD24.4 percentage of heavy drinking daysStandard Error 3.1
Suvorexant TreatmentPercentage of Heavy Drinking Days During Daily Use of Suvorexant.Week 2 PHDD29.5 percentage of heavy drinking daysStandard Error 3.9
p-value: 0.01Mixed Models Analysis
Primary

Startle Eyeblink Electromyographic (EMG) Response to Stress With an Acute Dose of Suvorexant

Startle EMG responses were collected during the well-validated No-Predictable-Unpredictable threat paradigm. The task includes within-subjects conditions and raw EMG responses were averaged for each condition. To quantify the difference between threat and no-threat periods, we calculated a standardized residual score for unpredictable threat (U-threat) by saving the variance leftover (i.e., the amount of variability in a dependent variable \[DV\] that is not explained by an independent variable \[IV\]) in a simple linear regression, where the no-threat EMG startle average (IV) was entered to predict the U-threat EMG startle average (DV). The U-threat residual score was used as the primary variable. It has a mean of zero and higher scores reflect greater startle reactivity to U-threat. U-threat residual scores were calculated for the baseline session and the acute challenge.

Time frame: Change from baseline to 2 hours post-ingestion of an acute dose of suvorexant.

Population: A total of 57 participants were included. Missing data was due to attrition, poor quality startle eyeblink data, or technical errors during startle data collection.

ArmMeasureGroupValue (MEAN)Dispersion
ControlStartle Eyeblink Electromyographic (EMG) Response to Stress With an Acute Dose of SuvorexantPre-Treatment Startle to U-threat0.01 Standardized residual scoresStandard Error 0.18
ControlStartle Eyeblink Electromyographic (EMG) Response to Stress With an Acute Dose of SuvorexantAcute Challenge Startle to U-threat0.01 Standardized residual scoresStandard Error 0.17
Suvorexant TreatmentStartle Eyeblink Electromyographic (EMG) Response to Stress With an Acute Dose of SuvorexantPre-Treatment Startle to U-threat.24 Standardized residual scoresStandard Error 0.19
Suvorexant TreatmentStartle Eyeblink Electromyographic (EMG) Response to Stress With an Acute Dose of SuvorexantAcute Challenge Startle to U-threat-0.18 Standardized residual scoresStandard Error 0.18
p-value: 0.1995% CI: [-0.2, 1.1]ANOVA
Primary

Startle Eyeblink Electromyographic (EMG) Response to Stress With Daily Use of Suvorexant.

Startle EMG responses were collected during the well-validated No-Predictable-Unpredictable threat paradigm. The task includes within-subjects conditions and raw EMG responses were averaged for each condition. To quantify the difference between threat and no-threat periods, we calculated a standardized residual score for unpredictable threat (U-threat) by saving the variance leftover (i.e., the amount of variability in a dependent variable \[DV\] that is not explained by an independent variable \[IV\]) in a simple linear regression, where the no-threat EMG startle average (IV) was entered to predict the U-threat EMG startle average (DV). The U-threat residual score was used as the primary variable. It has a mean of zero and higher scores reflect greater startle reactivity to U-threat.

Time frame: Change from baseline to post-treatment, up to 2 months.

Population: A total of 54 participants were included. Missing data was due to attrition, poor quality startle eyeblink data, or technical errors during startle data collection.

ArmMeasureGroupValue (MEAN)Dispersion
ControlStartle Eyeblink Electromyographic (EMG) Response to Stress With Daily Use of Suvorexant.Post-treatment Startle to U-threat0.08 Standardized residual scoresStandard Error 0.19
ControlStartle Eyeblink Electromyographic (EMG) Response to Stress With Daily Use of Suvorexant.Pre-Treatment Startle to U-threat-0.13 Standardized residual scoresStandard Error 0.14
Suvorexant TreatmentStartle Eyeblink Electromyographic (EMG) Response to Stress With Daily Use of Suvorexant.Post-treatment Startle to U-threat-0.23 Standardized residual scoresStandard Error 0.14
Suvorexant TreatmentStartle Eyeblink Electromyographic (EMG) Response to Stress With Daily Use of Suvorexant.Pre-Treatment Startle to U-threat0.28 Standardized residual scoresStandard Error 0.18
Comparison: We conducted a repeated measures analysis of variable with session (pre-treatment vs. post-treatment) as a within-subjects variable and treatment arm as a between-subjects variable. Standardized residual scores reflecting startle reactivity to unpredictable threat (\> no-threat) was the dependent variable.p-value: 0.0395% CI: [0.07, 1.38]ANOVA
Secondary

Changes in Neural Activation During Unpredictable Stress Anticipation Following Daily Use of Suvorexant.

Activation parameter estimates (arbitrary units) were extracted from anatomical bilateral aINS masks for each individual, pre and post treatment. Specifically, activation parameter estimates were extracted from anticipation of unpredictable threat \> anticipation of no-threat individual contrast maps for each scanning session. Greater values reflect greater activation in the bilateral insula during the anticipation of unpredictable threat. A repeated measures analysis of variance was used to test the session (time 1 vs. time 2) by treatment arm interaction on bilateral aINS activation during unpredictable threat. Significance was set at p \<.05

Time frame: Change from baseline to post-treatment, up to 2 months.

Population: A subset of participants were randomized to complete functional magnetic resonance imaging (fMRI) pre- and post-treatment. Only individuals with two scanning sessions were analyzed.

ArmMeasureGroupValue (MEAN)Dispersion
ControlChanges in Neural Activation During Unpredictable Stress Anticipation Following Daily Use of Suvorexant.Pre-Treatment Bilateral aINS0.330 arbitrary unitsStandard Error 0.141
ControlChanges in Neural Activation During Unpredictable Stress Anticipation Following Daily Use of Suvorexant.Post-Treatment Bilateral aINS0.482 arbitrary unitsStandard Error 0.153
Suvorexant TreatmentChanges in Neural Activation During Unpredictable Stress Anticipation Following Daily Use of Suvorexant.Pre-Treatment Bilateral aINS0.652 arbitrary unitsStandard Error 0.141
Suvorexant TreatmentChanges in Neural Activation During Unpredictable Stress Anticipation Following Daily Use of Suvorexant.Post-Treatment Bilateral aINS0.226 arbitrary unitsStandard Error 0.153
Comparison: A session (pre vs. post) by treatment arm (suvorexant vs. placebo) repeated measures analysis of variance (ANOVA) was performed. The effect of session was then probed within each treatment arm.p-value: <0.0595% CI: [-0.01, 1.2]ANOVA

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026