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Clinical Trial Summary

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


Clinical Trial 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. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06136195
Study type Interventional
Source Yale University
Contact Suchitra Krishnan, PhD
Phone 203-974-7595
Email suchitra.krishnan-sarin@yale.edu
Status Not yet recruiting
Phase Phase 2
Start date May 1, 2024
Completion date May 31, 2026

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