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Completed Phase 2 Interventional

A Study Evaluating the Safety and Clinical Activity of HCV-796 in Treatment-Naive and Non-Responder Subjects

ClinicalTrials.gov ID: NCT00367887

Public ClinicalTrials.gov record NCT00367887. 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 Oct 17, 2026, 5:44 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 2, Randomized, Open-Label Study Of The Safety, Antiviral Activity, And Pharmacokinetics Of HCV-796 Administered In Combination With Peginterferon Alfa 2B (Peg-Intron) Plus Ribavirin (Rebetol) Versus Peg-Intron Plus Rebetol In Subjects With Hepatitis C Virus Genotype 1 Infection

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This is a phase 2, randomized, open-label study comparing the safety, antiviral activity, and pharmacokinetics of HCV-796 administered in combination with peginterferon alfa 2B (Peg-Intron) plus concomitant Rebetol vs. Peg-Intron plus Rebetol in Hepatitis C Virus (HCV) genotype 1-infected subjects who are either naive to treatment or who have previously failed treatment (non-responders).

Study identification

NCT ID
NCT00367887
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Enrollment
246 participants

Conditions and interventions

Conditions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years to 65 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 2006 (Type not available)
Primary completion
Jul 2008 (Actual)
Completion
Jul 2008 (Actual)
Last update posted
Feb 11, 2013

2006 – 2008

United States locations

U.S. sites
34
U.S. states
16
U.S. cities
29
Facility City State ZIP Site status
Pfizer Investigational Site Anaheim California 92801 —
Pfizer Investigational Site La Jolla California 92037 —
Pfizer Investigational Site La Jolla California 92067 —
Pfizer Investigational Site Los Angeles California 90033 —
Pfizer Investigational Site Pasadena California 91105 —
Pfizer Investigational Site San Diego California 92123 —
Pfizer Investigational Site San Diego California 92161 —
Pfizer Investigational Site San Francisco California 94115 —
Pfizer Investigational Site San Francisco California 94121 —
Pfizer Investigational Site Washington D.C. District of Columbia 20010 —
Pfizer Investigational Site Gainesville Florida 32610 —
Pfizer Investigational Site Miami Florida 33136 —
Pfizer Investigational Site Atlanta Georgia 30309 —
Pfizer Investigational Site Louisville Kentucky 40202 —
Pfizer Investigational Site Boston Massachusetts 02215 —
Pfizer Investigational Site Worcester Massachusetts 01655 —
Pfizer Investigational Site Detroit Michigan 48202 —
Pfizer Investigational Site Plymouth Minnesota 55446 —
Pfizer Investigational Site Saint Paul Minnesota 55117 —
Pfizer Investigational Site St Louis Missouri 63104 —
Pfizer Investigational Site Albuquerque New Mexico 87131 —
Pfizer Investigational Site New York New York 10021 —
Pfizer Investigational Site New York New York 10032 —
Pfizer Investigational Site The Bronx New York 10461 —
Pfizer Investigational Site The Bronx New York 10468 —
Pfizer Investigational Site Chapel Hill North Carolina 27599-7209 —
Pfizer Investigational Site Durham North Carolina 27710 —
Pfizer Investigational Site Cincinnati Ohio 45219 —
Pfizer Investigational Site Cleveland Ohio 44195 —
Pfizer Investigational Site Philadelphia Pennsylvania 19141 —
Pfizer Investigational Site Houston Texas 77030 —
Pfizer Investigational Site Annandale Virginia 22003 —
Pfizer Investigational Site Fairfax Virginia 22031 —
Pfizer Investigational Site Richmond Virginia 23249 —

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 NCT00367887, 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 11, 2013 · Synced Oct 17, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00367887 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →