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Completed Phase 2Phase 3 Interventional Results available

A Study to Evaluate Treatment of Hepatitis C Virus Infection in Pediatric Subjects

ClinicalTrials.gov ID: NCT02486406

Public ClinicalTrials.gov record NCT02486406. 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 22, 2026, 9:34 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

An Open-Label, Multicenter Study to Evaluate the Pharmacokinetics, Safety, and Efficacy of Ombitasvir (OBV), Paritaprevir (PTV), Ritonavir (RTV) With or Without Dasabuvir (DSV) and With or Without Ribavirin (RBV) in Pediatric Subjects With Genotype 1 or 4 Chronic Hepatitis C Virus (HCV) Infection (ZIRCON)

Study identification

NCT ID
NCT02486406
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2, Phase 3
Lead sponsor
AbbVie
Industry
Enrollment
64 participants

Conditions and interventions

Interventions

  • Ombitasvir/paritaprevir/ritonavir Drug
  • Dasabuvir Drug
  • Ribavirin Drug
  • Ombitasvir mini tablet Drug
  • Paritaprevir mini tablet Drug
  • Ritonavir mini tablet Drug
  • Dasabuvir mini tablet Drug
  • Ribavirin solution Drug

Drug

Eligibility (public fields only)

Age range
3 Years to 17 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
Oct 27, 2015
Primary completion
Nov 18, 2020
Completion
Nov 18, 2020
Last update posted
Oct 4, 2021

2015 – 2020

United States locations

U.S. sites
11
U.S. states
9
U.S. cities
10
Facility City State ZIP Site status
UCSF Benioff Childrens Hosp /ID# 136774 San Francisco California 94158
Children's Hospital Colorado /ID# 137017 Aurora Colorado 80045
University of Florida - Archer /ID# 136830 Gainesville Florida 32610
Advent Health /ID# 167663 Orlando Florida 32803
Indiana University /ID# 137015 Indianapolis Indiana 46202
Boston Childrens Hospital /ID# 137174 Boston Massachusetts 02115
Boston Medical Center /ID# 136831 Boston Massachusetts 02118
Columbia Univ Medical Center /ID# 136431 New York New York 10032-3725
Children's Hospital of Philadelphia /ID# 137018 Philadelphia Pennsylvania 19104
Baylor College of Medicine /ID# 136590 Houston Texas 77030-3411
Seattle Children's Hospital /ID# 137019 Seattle Washington 98105

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 10 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02486406, 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 Oct 4, 2021 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02486406 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →