ClinicalTrials.Veeva

Menu

Novel mGluR5 Modulator Effects on Alcohol Drinking and MRI Outcomes

Medical University of South Carolina (MUSC) logo

Medical University of South Carolina (MUSC)

Status and phase

Completed
Phase 2
Phase 1

Conditions

Alcohol Use Disorder

Treatments

Drug: Placebo
Drug: GET73

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT04831684
Pro00102334

Details and patient eligibility

About

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.

Enrollment

79 patients

Sex

All

Ages

21 to 40 years old

Volunteers

No 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.

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

79 participants in 2 patient groups, including a placebo group

Group A
Placebo Comparator group
Treatment:
Drug: Placebo
Group B
Experimental group
Treatment:
Drug: GET73

Trial documents
1

Trial contacts and locations

1

Loading...

Central trial contact

Sara Hix

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems