drugset / Trial / NCT07325266

Human Laboratory Study of Apremilast for Alcohol Use Disorder

NCT07325266

RandomizedParallel-groupTriple-blindTreatment

Summary

Primary: The primary objective of this study is to compare the efficacy of two different maintenance doses of apremilast (tablets) in reducing alcohol craving among subjects with moderate to severe alcohol use disorder (AUD) after two weeks of daily dosing. Secondary: Secondary objectives include evaluation of two different maintenance doses of apremilast compared with matched placebo on other measures of self-reported alcohol consumption, alcohol craving, alcohol-related negative consequences, AUD symptoms, pain, sleep disturbances, depression, anxiety, quality of life, cigarette smoking, other nicotine use, cannabis use, retention in the study, and safety.

Timeline

Start
2026-04-03
Primary completion
2027-01-31
Completion
2027-07-31

Drugs

EvaluationDrugModalityDoseRoute
Comparator Apremilast Small molecule 60 mg Oral
Comparator Apremilast Small molecule 90 mg Oral

Indications