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Completed Phase 3 Interventional Results available

Efficacy and Safety of 8-weeks of Glecaprevir/Pibrentasvir in Treatment-Naïve Adults With HCV Genotype 1-6 and Aspartate Aminotransferase to Platelet Ratio Index (APRI) ≤1

ClinicalTrials.gov ID: NCT03212521

Public ClinicalTrials.gov record NCT03212521. 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 Jun 25, 2026, 1:16 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 Single Arm, Open Label, Multicenter Study to Evaluate the Efficacy and Safety of Glecaprevir (GLE)/Pibrentasvir (PIB) in Treatment Naïve Adults With Chronic Hepatitis C Virus (HCV) Genotypes 1 - 6 Infection and Aspartate Aminotransferase to Platelet Ratio Index (APRI) ≤ 1

Study identification

NCT ID
NCT03212521
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
AbbVie
Industry
Enrollment
230 participants

Conditions and interventions

Interventions

  • Glecaprevir/Pibrentasvir Drug

Drug

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
Aug 6, 2017
Primary completion
Aug 12, 2018
Completion
Aug 12, 2018
Last update posted
Sep 3, 2019

2017 – 2018

United States locations

U.S. sites
11
U.S. states
10
U.S. cities
10
Facility City State ZIP Site status
Parkway Medical Center /ID# 161261 Birmingham Alabama 35215
Arkansas Gastroenterology /ID# 161266 North Little Rock Arkansas 72117
UC Davis Medical Center /ID# 161138 Sacramento California 95817
Yale University /ID# 161258 New Haven Connecticut 06510
Univ Maryland School Medicine /ID# 161157 Baltimore Maryland 21201
Digestive Disease Associates - Baltimore /ID# 161260 Baltimore Maryland 21229
University of Michigan Hospitals /ID# 161265 Ann Arbor Michigan 48109-5008
Northwest Gastroenterology Cli /ID# 161257 Portland Oregon 97210
Liver Associates of Texas, P.A /ID# 161262 Houston Texas 77030-2783
University of Vermont Medical Center /ID# 161263 Burlington Vermont 05401-1473
Digestive and Liver Disease Sp /ID# 161259 Norfolk Virginia 23502

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 31 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03212521, 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 Sep 3, 2019 · Synced Jun 25, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03212521 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →