Integrated Approaches for Identifying Molecular Targets in Alcoholic Hepatitis

Alcoholic Hepatitis Clinical Trial

— InTeam  

Official title:

Integrated Approaches for Identifying Molecular Targets in Alcoholic Hepatitis

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02075918
• Other study ID #: 12-2016
• Secondary ID: 1U01AA021908-01
• Status: Completed
• Start date: May 2014
• Est. completion date: May 31, 2019

Study information

• Verified date: June 2019
• Source: University of Pittsburgh
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

Purpose: To improve the diagnosis and assessment of severity of acute alcoholic hepatitis Participants: Patients admitted to one of ten centers with acute alcoholic hepatitis Procedures (methods): Consecutive patients admitted with acute alcoholic hepatitis will be enrolled in an NIH U01 study of acute alcoholic hepatitis where liver tissue, blood and stool will be collected to discover and validate factors associated with diagnosis, severity of disease and survival.

Description:

The development of new targeted therapies for alcoholic hepatitis (AH) is one of the more urgent needs in clinical hepatology. To reach this goal, large multidisciplinary networks are required. The proposed initiative "Integrated Approaches for Identifying Molecular Targets in Alcoholic Hepatitis" (InTeam) will coordinate a multidisciplinary group composed of clinicians, physician-scientists, basic scientists and bioinformatics experts. The overarching hypothesis of InTeam is that the most rational way to provide a useful framework for future clinical trials in (AH) consists of the (i) determination of key drivers of the disease process, (ii) classification of molecular profiles and subtypes of AH, and (iii) identification of "druggable" targets based on both key drivers and molecular classification. Moreover, mouse models for AH are lacking making it impossible to evaluate promising targets in preclinical mouse studies in a meaningful manner. For this purpose, InTeam will integrate data obtained from molecular pathology studies in human AH and functional studies of key pathways in animal models. The proposed InTeam consortium includes three research projects, ten clinical centers, a Human Biorepository and a Mouse Models Core. The Human Biorepository Core will generate the to-date largest collection of samples from patients with AH from 10 academic liver centers and a comprehensive database that will serve as a basis for the proposed translational studies and be a valuable asset for the broader scientific community. The Mouse Models core will conduct murine studies after establishing and evaluating mouse models of AH based on the pathophysiology and molecular drivers of human AH determined by this consortium.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 376
• Est. completion date: May 31, 2019
• Est. primary completion date: May 2019
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 70 Years

Eligibility

Inclusion Criteria:

• Patients 18 = and = 70 years of age.

• Active alcohol abuse within the past 3 months.

• Has an Aspartate Aminotransferase (AST) > Alanine Aminotransferase (ALT).

• Elevated Total Bilirubin level > 3.0.

• Absence of autoimmune liver disease (ANA>1/320).

• Absence of hepatitis B infection.

• A liver biopsy, and/or a clinical picture consistent with alcoholic hepatitis.

• The "Start Date" (is the date of the liver biopsy or = to 1 week [72 hours is preferred] from the time of admission).

Exclusion Criteria:

• Hepatocellular carcinoma.

• Complete portal vein thrombosis.

• Advanced or terminal extrahepatic diseases.

• Lack of consent to participate in the study.

• Pregnancy.

• Received more than 3 days of treatment with (prednisolone or pentoxifyllin) prior to start date.

Control patients

Related Conditions & MeSH terms

• Alcoholic Hepatitis
• Control Patients
• Hepatitis
• Hepatitis A
• Hepatitis, Alcoholic

Locations

Country	Name	City	State
United States	University of Pittsburgh	Pittsburgh	Pennsylvania

Sponsors (12)

Lead Sponsor	Collaborator
University of Pittsburgh	Columbia University, Hospital San Jose Tec de Monterrey, Hospital Vall d'Hebron, Institut National de la Santé Et de la Recherche Médicale, France, King's College London, National Institute on Alcohol Abuse and Alcoholism (NIAAA), University of Alberta, University of Wisconsin, Madison, Veterans Medical Research Foundation, Weill Medical College of Cornell University, Yale University

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Diagnosis and Severity of Alcoholic Hepatitis	Utilizing liver tissue, blood samples, and stool and urine samples, InTeam will aim to discover and validate factors associated with the diagnosis and severity of Alcoholic hepatitis.	3 months after end of Study
Secondary	Major Liver Complications	As an observational study, we will collect data regarding major liver complications such as, ascites, renal failure, encephalopathy, and bleeding.	3 months after end of study
Secondary	Death/Transplantation	As an observational study, we will collect the data regarding number the survival of Alcoholic Hepatitis by considering deaths and transplantations.	3 months after end of study