ClinicalTrials.gov record
Completed Phase 2 Interventional Results available

A Study of TMC435 in Combination With PSI-7977 (GS7977) in Chronic Hepatitis C Genotype 1-Infected Prior Null Responders To Peginterferon/Ribavirin Therapy or HCV Treatment-Naive Patients

ClinicalTrials.gov ID: NCT01466790

Public ClinicalTrials.gov record NCT01466790. 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 May 20, 2026, 6:43 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

An Exploratory Phase IIa, Randomized, Open-Label Trial to Investigate the Efficacy and Safety of 12 Weeks or 24 Weeks of TMC435 in Combination With PSI-7977 (GS7977) With Or Without Ribavirin in Chronic Hepatitis C Genotype 1-Infected Prior Null Responders To Peginterferon/Ribavirin Therapy or HCV Treatment-Naive Subjects

Study identification

NCT ID
NCT01466790
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Janssen R&D Ireland
Industry
Enrollment
168 participants

Conditions and interventions

Conditions

Interventions

  • PSI-7977 (GS7977) Drug
  • Ribavirin Drug
  • TMC435 Drug

Drug

Eligibility (public fields only)

Age range
18 Years to 70 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
Dec 31, 2011
Primary completion
Oct 31, 2013
Completion
Dec 31, 2013
Last update posted
Feb 8, 2015

2012 – 2014

United States locations

U.S. sites
22
U.S. states
13
U.S. cities
22
Facility City State ZIP Site status
Not listed Hoover Alabama
Not listed Bakersfield California
Not listed La Jolla California
Not listed San Diego California
Not listed New Haven Connecticut
Not listed Brandenton Florida
Not listed Jacksonville Florida
Not listed Orlando Florida
Not listed Tampa Florida
Not listed Wellington Florida
Not listed Atlanta Georgia
Not listed Chicago Illinois
Not listed Lutherville Maryland
Not listed Lebanon New Hampshire
Not listed New York New York
Not listed Pittsburgh Pennsylvania
Not listed Arlington Texas
Not listed Dallas Texas
Not listed San Antonio Texas
Not listed Falls Church Virginia
Not listed Norfolk Virginia
Not listed Seatle Washington

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 1 non-U.S. site.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01466790, 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 8, 2015 · Synced May 20, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01466790 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →