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Completed Phase 3 Interventional

Civacir® Polyclonal Immune Globulin (IgG) to Prevent Hepatitis C Virus (HCV) Recurrence in Liver Transplant Patients.

ClinicalTrials.gov ID: NCT01804829

Public ClinicalTrials.gov record NCT01804829. 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, 7:03 AM 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 Multi-Center, Randomized, Prospective, Open-Label Phase III Study to Evaluate the Efficacy, Safety and Pharmacokinetics of Hepatitis C Immune Globulin Intravenous (Human), Civacir®, in Orthotopic Liver Transplant Recipients

Study identification

NCT ID
NCT01804829
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Biotest Pharmaceuticals Corporation
Industry
Enrollment
80 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 80 Years
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
May 31, 2013
Primary completion
Jan 31, 2016
Completion
May 31, 2016
Last update posted
Mar 14, 2017

2013 – 2016

United States locations

U.S. sites
23
U.S. states
13
U.S. cities
18
Facility City State ZIP Site status
University of Southern California / Keck Hospital Los Angeles California 90033
University of California San Francisco San Francisco California 94143
University of Miami Miller School of Medicine Miami Florida 33136
Florida Hospital Transplant Institute Orlando Florida 32804
Piedmont Hospital Atlanta Georgia 30309
Emory University School of Medicine Atlanta Georgia 30322
Northwestern Memorial Hospital Chicago Illinois 60611
University of Kentucky Chandler Medical Center Lexington Kentucky 40536
Ochsner Medical Center New Orleans Louisiana 70121
Beth Israel Deaconess Medical Center Boston Massachusetts 02215
Lahey Hospital Burlington Massachusetts 01805
NYU Langone Medical Center New York New York 10016
The Mount Sinai Medical Center New York New York 10029
Columbia University College of Physicians and Surgeons New York New York 10032
Oregon Health & Science University Portland Oregon 97239
Methodist University Hospital Memphis Tennessee 38104
Vanderbilt University Medical Center Nashville Tennessee 37232
Baylor University Medical Center Dallas Texas 75246
Advanced Liver Therapies / St. Luke's Episcopal Hospital Houston Texas 77030
Houston Methodist Hospital Houston Texas 77030
Houston Methodist Houston Texas 77030
University of Utah Health Sciences Center Salt Lake City Utah 84112
University of Virginia Health System Charlottesville Virginia 22908

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01804829, 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 Mar 14, 2017 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01804829 live on ClinicalTrials.gov.

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