Integrated Therapies for Alcohol Use in Alcohol-associated Liver Disease (ITAALD) Trial
Samer Gawrieh
216 participants
Jan 27, 2026
INTERVENTIONAL
Conditions
Summary
This is a multicenter, randomized, double-blinded, placebo-controlled trial focused on the treatment of severe alcohol-associated hepatitis (sAH) and alcohol use disorder (AUD). The primary purpose of the study is to determine whether subjects receiving sAH therapy in addition to AUD treatments will have better alcohol and liver-related outcomes at 6 months compared to sAH therapy plus usual care for AUD. Patients assigned to the AUD treatment will receive Acamprosate and counseling whereas those assigned to AUD standard care will receive brief advice and referral to a 12-step program. The secondary purpose of the study is to determine if F-652 is safe and effective in treating sAH when compared to prednisone. Subjects will receive F-652 on days 1 and 7 or prednisone for 28 days. Outcomes will be measured by overall survival at 90 days.
Eligibility
Plain Language Summary
Simplified for easier understanding
This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.
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Interventions
F-652 (IL-22) is a fusion protein of human IL-22 with IgG2 fragment, and has anti-inflammatory effects
Prednisone is an adrenal glucocorticoid with anti-inflammatory effects
Acamprosate is a propane-1 sulfonic acid with anti-ethanol dependency effects
Matching placebo
Matching Placebo
MI is an evidence-based counseling style to overcome ambivalence to treatment in AUD patients
MET is an MI-based approach that includes 2-4 behavioral treatment sessions based on the Platform Treatment Manual
defined as a brief intervention with advice not to drink alcohol-containing beverages and referral to a 12-step program
Locations(6)
View Full Details on ClinicalTrials.gov
For the most up-to-date information, visit the official listing.
NCT07060638