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Terminated Phase 3 Interventional Results available

To Assess Safety/Efficacy of ELAD in Subjects w/ Severe Acute Alcoholic Hepatitis (sAAH) and Lille Score Failure

ClinicalTrials.gov ID: NCT01829347

Public ClinicalTrials.gov record NCT01829347. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 21, 2026, 4:45 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Randomized, Open-Label, Multicenter, Controlled Study to Assess Safety and Efficacy of ELAD® in Subjects With Severe Acute Alcoholic Hepatitis (sAAH) and Lille Score Failure

Study identification

NCT ID
NCT01829347
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 3
Lead sponsor
Vital Therapies, Inc.
Industry
Enrollment
18 participants

Conditions and interventions

Interventions

  • ELAD Biological
  • Standard of Care treatment Other

Biological · Other

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Mar 31, 2014
Primary completion
Sep 30, 2015
Completion
Aug 31, 2018
Last update posted
Feb 18, 2019

2014 – 2018

United States locations

U.S. sites
21
U.S. states
17
U.S. cities
19
Facility City State ZIP Site status
University of Arkansas for Medical Sciences Little Rock Arkansas 72205
University of California San Diego San Diego California 92103
Georgetown University Hospital Washington D.C. District of Columbia 20007
University of Miami Hospital Miami Florida 33136
Cleveland Clinic Florida Weston Florida 33331
Piedmont Atlanta Hospital Atlanta Georgia 30309
Emory University Hospital Atlanta Georgia 30322
Johns Hopkins University Hospital Bethesda Maryland 20814
Beth Israel Deaconess Medical Center Boston Massachusetts 02215
University of Minnesota Medical Center - Twin Cities Campus Minneapolis Minnesota 55455
University of Nebraska Medical Center Omaha Nebraska 68198
Rutgers University Hospital Newark New Jersey 07101
North Shore University Hospital Manhasset New York 11030
Montefiore Medical Center The Bronx New York 10467
Carolinas Medical Center Charlotte North Carolina 28204
Cleveland Clinic Foundation Cleveland Ohio 44195
Drexel University College of Medicine Philadelphia Pennsylvania 19102
Albert Einstein Medical Center Philadelphia Pennsylvania 19141
University of Texas Health Science Center, San Antonio San Antonio Texas 78215
Swedish Medical Center Seattle Washington 98104
Aurora St. Luke's Medical Center Milwaukee Wisconsin 53215

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 18 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01829347, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Feb 18, 2019 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01829347 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →