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Novel mGluR5 Modulator Effects on Alcohol Drinking and MRI Outcomes

Primary Purpose

Alcohol Use Disorder

Status
Recruiting
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
Placebo
GET73
Sponsored by
Medical University of South Carolina
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Alcohol Use Disorder

Eligibility Criteria

21 Years - 40 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Age 21-40 (to focus on an age group still on a trajectory of increasing alcohol consumption, consistent with our pilot data and past iterations of the ARC).
  2. Meets Diagnostic and Statistical Manual of Mental Disorders, 5th edition (DSM-5) criteria for current Alcohol Use Disorder, with at least Moderate severity.
  3. Reports drinking, on average, at least 20 standard alcoholic drinks per week for at least the past 3 months.
  4. Currently not engaged in, and does not want treatment for, alcohol-related problems.
  5. Able to read and understand questionnaires and informed consent.
  6. Lives within 50 miles of the study site.
  7. Able to maintain abstinence from alcohol the evening prior to appointments (without the aid of detoxification medications), as determined by self-report and breathalyzer measurements.
  8. Amenable to drinking liquor in fruit juice.

Exclusion Criteria:

  1. Current DSM-5 diagnosis of any other substance use disorder except Nicotine Use Disorder.
  2. Any psychoactive substance use (except marijuana and nicotine) within the last 30 days, as indicated by self-report and urine drug screen. For marijuana, no use within the last seven days by verbal report and negative (or decreasing) urine THC levels.
  3. Current DSM-5 Axis I diagnosis, including major depression, panic disorder, obsessive-compulsive disorder, post-traumatic stress disorder, bipolar affective disorder, schizophrenia, dissociative disorders, eating disorders, or any other psychotic or organic mental disorder.
  4. Current suicidal ideation or homicidal ideation.
  5. Using CYP2C19 and/or CYP3A4 inhibitors or inducers in the 14 days before dosing or during the study.
  6. Need for maintenance or acute treatment with any psychoactive medication, including antiepileptic medications.
  7. Currently taking medication known to affect alcohol intake (e.g., disulfiram, naltrexone, acamprosate, topiramate).
  8. History of severe alcohol withdrawal (e.g., tremor, sweating, anxiety, seizure, delirium tremens), as evidenced by self-report and assessment with Clinical Institute Withdrawal Assessment for Alcohol-Revised (CIWA-Ar).
  9. Clinically significant medical problems such as cardiovascular, renal, gastrointestinal, or endocrine problems that would impair participation or limit medication ingestion.
  10. Past alcohol-related medical illness, such as gastrointestinal bleeding, pancreatitis, or peptic ulcer.
  11. Has hepatocellular disease indicated by elevations of SGPT (ALT) or SGOT (AST) greater than 2.5 times normal at screening.
  12. Females of childbearing potential who are pregnant (by urine HCG), nursing, or who are not using a reliable form of birth control.
  13. Current charges pending for a violent crime (not including DUI-related offenses).
  14. Lack of a stable living situation.
  15. Presence of ferrous metal in the body, as evidenced by metal screening and self-report.
  16. Severe claustrophobia or extreme obesity that preclude placement in the MRI scanner.
  17. Neurological disease or history of head injury with > 2 minutes of unconsciousness.

Sites / Locations

  • Charleston Alcohol Research Center, Institute of Psychiatry, Medical University of South CarolinaRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Placebo Comparator

Experimental

Arm Label

Group A

Group B

Arm Description

Outcomes

Primary Outcome Measures

Number of drinks consumed during bar-lab paradigm (free drinking period)
Change in Gamma aminobutyric acid (GABA) and glutamate levels
Acquired via spectroscopy sequence completed at baseline and day 7 scans
Levels of cortical activation to visual cues of alcohol
Acquired via functional magnetic resonance imaging completed at baseline and day 7 scans

Secondary Outcome Measures

Full Information

First Posted
April 1, 2021
Last Updated
January 19, 2023
Sponsor
Medical University of South Carolina
Collaborators
National Institutes of Health (NIH), National Institute on Alcohol Abuse and Alcoholism (NIAAA)
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1. Study Identification

Unique Protocol Identification Number
NCT04831684
Brief Title
Novel mGluR5 Modulator Effects on Alcohol Drinking and MRI Outcomes
Official Title
Effects of a Novel mGluR5 Negative Allosteric Modulator on Alcohol Drinking, Neurochemistry, and Brain Reactivity to Alcohol Cues in Alcohol Use Disorder
Study Type
Interventional

2. Study Status

Record Verification Date
January 2023
Overall Recruitment Status
Recruiting
Study Start Date
September 15, 2021 (Actual)
Primary Completion Date
April 15, 2026 (Anticipated)
Study Completion Date
April 22, 2026 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Medical University of South Carolina
Collaborators
National Institutes of Health (NIH), National Institute on Alcohol Abuse and Alcoholism (NIAAA)

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
This study evaluates the effects of the medication GET73 among non-treatment-seeking individuals who regularly drink alcohol. Participants in the study will take GET73 or placebo for an 8-day study. There are 4 study visits including 2 MRI scans.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Alcohol Use Disorder

7. Study Design

Primary Purpose
Basic Science
Study Phase
Phase 1, Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
90 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Group A
Arm Type
Placebo Comparator
Arm Title
Group B
Arm Type
Experimental
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Participants will be getting placebo for 8 days of dosing.
Intervention Type
Drug
Intervention Name(s)
GET73
Intervention Description
Participants will be getting GET73 for 8 days of dosing.
Primary Outcome Measure Information:
Title
Number of drinks consumed during bar-lab paradigm (free drinking period)
Time Frame
165 minutes
Title
Change in Gamma aminobutyric acid (GABA) and glutamate levels
Description
Acquired via spectroscopy sequence completed at baseline and day 7 scans
Time Frame
baseline to day 7
Title
Levels of cortical activation to visual cues of alcohol
Description
Acquired via functional magnetic resonance imaging completed at baseline and day 7 scans
Time Frame
baseline to day 7

10. Eligibility

Sex
All
Minimum Age & Unit of Time
21 Years
Maximum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age 21-40 (to focus on an age group still on a trajectory of increasing alcohol consumption, consistent with our pilot data and past iterations of the ARC). Meets Diagnostic and Statistical Manual of Mental Disorders, 5th edition (DSM-5) criteria for current Alcohol Use Disorder, with at least Moderate severity. Reports drinking, on average, at least 20 standard alcoholic drinks per week for at least the past 3 months. Currently not engaged in, and does not want treatment for, alcohol-related problems. Able to read and understand questionnaires and informed consent. Lives within 50 miles of the study site. Able to maintain abstinence from alcohol the evening prior to appointments (without the aid of detoxification medications), as determined by self-report and breathalyzer measurements. Amenable to drinking liquor in fruit juice. Exclusion Criteria: Current DSM-5 diagnosis of any other substance use disorder except Nicotine Use Disorder. Any psychoactive substance use (except marijuana and nicotine) within the last 30 days, as indicated by self-report and urine drug screen. For marijuana, no use within the last seven days by verbal report and negative (or decreasing) urine THC levels. Current DSM-5 Axis I diagnosis, including major depression, panic disorder, obsessive-compulsive disorder, post-traumatic stress disorder, bipolar affective disorder, schizophrenia, dissociative disorders, eating disorders, or any other psychotic or organic mental disorder. Current suicidal ideation or homicidal ideation. Using CYP2C19 and/or CYP3A4 inhibitors or inducers in the 14 days before dosing or during the study. Need for maintenance or acute treatment with any psychoactive medication, including antiepileptic medications. Currently taking medication known to affect alcohol intake (e.g., disulfiram, naltrexone, acamprosate, topiramate). History of severe alcohol withdrawal (e.g., tremor, sweating, anxiety, seizure, delirium tremens), as evidenced by self-report and assessment with Clinical Institute Withdrawal Assessment for Alcohol-Revised (CIWA-Ar). Clinically significant medical problems such as cardiovascular, renal, gastrointestinal, or endocrine problems that would impair participation or limit medication ingestion. Past alcohol-related medical illness, such as gastrointestinal bleeding, pancreatitis, or peptic ulcer. Has hepatocellular disease indicated by elevations of SGPT (ALT) or SGOT (AST) greater than 2.5 times normal at screening. Females of childbearing potential who are pregnant (by urine HCG), nursing, or who are not using a reliable form of birth control. Current charges pending for a violent crime (not including DUI-related offenses). Lack of a stable living situation. Presence of ferrous metal in the body, as evidenced by metal screening and self-report. Severe claustrophobia or extreme obesity that preclude placement in the MRI scanner. Neurological disease or history of head injury with > 2 minutes of unconsciousness.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Sara Hix
Phone
843-792-0572
Email
hixs@musc.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
James Prisciandaro
Organizational Affiliation
Medical University of South Carolina
Official's Role
Principal Investigator
Facility Information:
Facility Name
Charleston Alcohol Research Center, Institute of Psychiatry, Medical University of South Carolina
City
Charleston
State/Province
South Carolina
ZIP/Postal Code
29425
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Sara Hix
Phone
843-792-0572
Email
hixs@musc.edu

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
Per NOT-AA-19-020, this study will submit and share data with NIAAA Data Archive, a data repository housed within the NIMH Data Archive. This includes broad sharing of all research subjects' de-identified data.
IPD Sharing Time Frame
De-identified participant data will be uploaded to the NIMH Data Archive twice yearly (by April 1 and October 1) during the course of this study, and will remain available with no end date.
IPD Sharing Access Criteria
Data and supporting documentation submitted to the NIMH Data Archive may be accessed and used broadly by approved users for research and other activities as authorized by and consistent with law.
IPD Sharing URL
https://nda.nih.gov/niaaa/award/data-sharing-expectations.html

Learn more about this trial

Novel mGluR5 Modulator Effects on Alcohol Drinking and MRI Outcomes

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