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Completed Phase 2 Interventional

Safety, Tolerability, and Antiviral Activity of ANA598 Administered in Combination With Pegylated Interferon and Ribavirin for the Treatment of Genotype-1 Chronic HCV Infection

ClinicalTrials.gov ID: NCT00978497

Public ClinicalTrials.gov record NCT00978497. 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 26, 2026, 4:56 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, Double-Blind, Placebo-Controlled, Ascending Multiple Dose Trial of the Safety, Efficacy, and Pharmacokinetics of ANA598 Administered With Pegylated Interferon and Ribavirin in Treatment-Naïve Genotype 1 Patients With Chronic Hepatitis C Infection

Study identification

NCT ID
NCT00978497
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Hoffmann-La Roche
Industry
Enrollment
97 participants

Conditions and interventions

Conditions

Interventions

  • placebo Drug
  • ANA598 Drug
  • Peginterferon Drug
  • Ribavirin Drug

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
Aug 31, 2009
Primary completion
Mar 31, 2010
Completion
Jul 31, 2011
Last update posted
Mar 30, 2017

2009 – 2011

United States locations

U.S. sites
20
U.S. states
11
U.S. cities
20
Facility City State ZIP Site status
United States, California 1 Anaheim California 92801
United States, California 4 Los Angeles California 90048
United States, California 2 San Clemente California 92673
United States, California 3 San Diego California 92120
United States, California 5 San Francisco California 33136
United States, Florida 2 Gainesville Florida 32601
United States, Florida 3 Miami Florida 33136
United States, Florida 1 Sarasota Florida 34209
United States, Maryland Lutherville Maryland 21093
United States, Massachusetts Boston Massachusetts 02215
United States, Michigan Detroit Michigan 48202
United States, New York New York New York 10021
United States, North Carolina Chapel Hill North Carolina 27514
United States, North Carolina Durham North Carolina 27705
United States, Ohio Cincinnati Ohio 45267
United States, Pennsylvania Philadelphia Pennsylvania 19104
United States, Texas 2 Houston Texas 77073
United States, Texas 1 San Antonio Texas 78215
United States, Virginia 1 Fairfax Virginia 22031
United States, Virginia 2 Falls Church Virginia 22042

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 NCT00978497, 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 Mar 30, 2017 · Synced Jun 26, 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 NCT00978497 live on ClinicalTrials.gov.

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