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Completed Phase 2 Interventional

A Study of Mericitabine in Combination With Telaprevir and Peginterferon Alfa-2a / Ribavirin in Participants With Chronic Hepatitis C

ClinicalTrials.gov ID: NCT01482390

Public ClinicalTrials.gov record NCT01482390. 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, 12:02 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 Phase II, Randomized, Double-Blind, Multicenter, Parallel Group Study to Evaluate the Sustained Virologic Response of the HCV Polymerase Inhibitor Prodrug RO5024048 in Combination With Telaprevir and Pegasys®/Copegus® in Patients With Chronic Hepatitis C Genotype 1 Virus Infection Who Were Prior Null Responders to Treatment With Pegylated Interferon/Ribavirin

Study identification

NCT ID
NCT01482390
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Hoffmann-La Roche
Industry
Enrollment
80 participants

Conditions and interventions

Conditions

Interventions

  • Ribavirin Drug
  • Mericitabine Drug
  • Peginterferon Alfa-2a Drug
  • Placebo Drug
  • Telaprevir 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
Nov 29, 2011
Primary completion
Jan 30, 2014
Completion
Jan 30, 2014
Last update posted
Apr 23, 2017

2011 – 2014

United States locations

U.S. sites
15
U.S. states
13
U.S. cities
15
Facility City State ZIP Site status
Birmingham Gastro Associates, P.C. Birmingham Alabama 35209
VA Long Beach Healthcare System Long Beach California 90822
Kaiser Permanente Sacramento Medical Center Sacramento California 95825
UCSD Antiviral Research Center San Diego California 92103
Yale University New Haven Connecticut 06510
Gastroenterology Group of Naples Naples Florida 34102
John Hopkins Hospital Lutherville Maryland 21093
Metrowest Medical Center Framingham Massachusetts 01702
Saint Louis University Gastroenterology & Hepatology; Clinical Research Unit St Louis Missouri 63104
Weill Cornell Medical College New York New York 10021
Carolina'S Center For Liver Disease Statesville North Carolina 28677
Uni of Cincinnati College of Medicine; Div. of Digestive Diseases Cincinnati Ohio 45267-0595
Baylor Uni Medical Center; Division Of Hepatology/Transplantation; Annette C. and Harold C. Simmons Dallas Texas 75246
McGuire; Veteran Affairs Med Ctr Richmond Virginia 23249
Harborview Medical Center Seattle Washington 98104

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 24 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01482390, 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 Apr 23, 2017 · Synced Jun 25, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01482390 live on ClinicalTrials.gov.

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