Influence of Mavoglurant on Alcohol Craving and Drinking in Heavy Drinkers

Alcohol Consumption Clinical Trial

Official title:

Influence of Mavoglurant on Alcohol Craving and Drinking in Heavy Drinkers

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT06136195
• Other study ID #: 2000029675
• Secondary ID: 2P50AA012870-21
• Status: Not yet recruiting
• Phase: Phase 2
• Start date: May 1, 2024
• Est. completion date: May 31, 2026

Study information

• Verified date: March 2024
• Source: Yale University
• Contact: Suchitra Krishnan, PhD
• Phone: 203-974-7595
• Email: suchitra.krishnan-sarin[@]yale.edu
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this research study is to find out about the effects of a drug called mavoglurant on alcohol consumption.

Description:

This project will use a double-blind, placebo-controlled, within-subject design to examine mavoglurant effects on alcohol craving, drinking, and subjective responses. Non-treatment seeking, heavy drinkers with Alcohol Use Disorder (AUD) will undergo 2 lab sessions, which include a Cue Exposure (craving) Paradigm (CEP) and an Alcohol Drinking Paradigm (ADP), as well as 1-week and 1-month follow up appointments. Prior to the first lab session, participants will be randomized to receive either 200 mg of mavoglurant or placebo. For the second lab session, participants will receive the other condition, mavoglurant or placebo, that they did not receive in the first lab session. Each session will be separated by at least a 5-8 day washout period to allow for complete washout of mavoglurant. This is followed by 1-week and 1-month follow up appointments.

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 63
• Est. completion date: May 31, 2026
• Est. primary completion date: May 31, 2026
• Accepts healthy volunteers: No
• Gender: All
• Age group: 21 Years to 50 Years

Eligibility

Inclusion Criteria:

1. Ages 21-50 (The lower limit is to avoid offering alcohol to individuals below the drinking age of 21. The upper age is determined by experience recruiting for our prior studies).

2. Ability to read English at 6th grade level or higher.

3. Meet DSM-V criteria for moderate or severe Alcohol Use Disorder (AUD).

4. Average weekly alcohol consumption of 30-70 standard drinks for men and 20-65 drinks for women. The lower limits are consistent with the lower sex-specific cut-offs defining high-risk drinking based on World Health Organization Risk Levels (WHO, 2000); the upper limits are designed to avoid recruiting participants whose drinking is likely to exceed the number of drinks available in the Alcohol Drinking Paradigm (ADP).

Exclusion Criteria:

1. Individuals who are seeking alcohol treatment or have been in alcohol treatment within the past 6 months.

2. Meet current Diagnostic and Statistical Manual v.5 (DSM-V) criteria for substance use disorder, except for tobacco use disorder or mild cannabis use disorder.

3. Positive urine drug screens at more than 1 baseline appointment for opiates, cocaine, benzodiazepines and barbiturates.

4. Psychotic or other severe psychiatric disorders as determined by clinical evaluation (Structured Clinical Interview for DSM-V; SCID). Note that if a subject endorses any harm/risk behaviors (e.g. suicidal/homicidal risk) a licensed clinician will be consulted immediately.

5. Regular use of psychoactive drugs, except for individuals on a stable dose of an antidepressant for at least 2 months.

6. Medical conditions that would contraindicate the consumption of alcohol or use of mavoglurant.

7. Clinically significant abnormalities in screening laboratories, including aspartate aminotransferase (AST) >1.5 times upper limit of normal (ULN); alanine aminotransferase (ALT) > 1.5 times ULN; total bilirubin >1.5 times ULN; serum creatinine >2.0 times ULN.

8. Neurological trauma or disease, delirium or hallucinations, or clinically significant or unstable medical conditions, including uncontrolled hypertension or diabetes, or significant cardiac, pulmonary, renal, hepatic, endocrine, or other systemic diseases, which in the opinion of the study physician and Principal Investigator, may put the patient at risk because of participation in the study.

9. Clinical Institute Withdrawal Assessment for Alcohol (CIWA-Ar) scores of 8 or greater or a history of significant repeated alcohol withdrawals to reduce the likelihood of withdrawal symptomatology if subjects reduce their drinking.

10. Women who are pregnant or nursing.

11. Participants who refuse to use a reliable method of birth control.

12. Subjects who report disliking spirits will be excluded because hard liquor will be provided during the ADP.

13. Subjects who have taken any investigational drug within 4 weeks of the anticipated date of the first study dose.

14. Individuals who report heavy drinking days in the 2 days prior to their intake appointment but have a negative ethyl glucuronide (EtG) test to rule out subjects who are misrepresenting their drinking history.

15. Subjects who have donated blood within the past 6 weeks.

Related Conditions & MeSH terms

• Alcohol Consumption
• Alcohol Drinking
• Alcohol Use Disorder (AUD)
• Alcoholic Intoxication
• Alcoholism
• Heavy Drinker

Intervention

Drug:
• Mavoglurant
The 200mg mavoglurant will be administered in the form of two 100mg oral tablets. Placebo will be administered with matching tablets.

Locations

Country	Name	City	State
United States	Yale New Haven Hospital	New Haven	Connecticut

Sponsors (2)

Lead Sponsor	Collaborator
Yale University	National Institute on Alcohol Abuse and Alcoholism (NIAAA)

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change in the number of drinks consumed	The number of drinks consumed during the adlib session will be recorded	Lab Session 1 (Day 1); Lab Session 2 (5-8 days after Lab Session 1).
Primary	Change in craving for alcohol	The Cue Exposure Paradigm (CEP) is used to measure craving for alcohol. The task uses a questionnaire that is in the form of a Visual Analog Scale (VAS). The endpoints will be marked with a 0 on the left indicating no craving and a 20 on the right indicating severe craving. Participants will indicate how strong they are craving to drink alcohol. The VAS takes 2-3 minutes to complete.	Lab Session 1 (Day 1); Lab Session 2 (5-8 days after Lab Session 1).