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Completed Phase 2 Interventional

Study of BMS-650032 With Peginterferon Alfa-2a Plus Ribavirin

ClinicalTrials.gov ID: NCT01030432

Public ClinicalTrials.gov record NCT01030432. 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 19, 2026, 12:36 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 2a/2b Study of BMS-650032 in Combination With Peginterferon Alfa-2a (Pegasys) and Ribavirin (Copegus) in Treatment-Naive Subjects With Genotypes 1 and 4 Chronic Hepatitis C Infection

Brief summary

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

The purpose of this study is to identify one or more doses of BMS-650032 that, when used in combination with pegylated-interferon alpha and ribavirin are safe and demonstrate sufficient activity against hepatitis C virus (Genotypes 1 and 4).

Study identification

NCT ID
NCT01030432
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Bristol-Myers Squibb
Industry
Enrollment
285 participants

Conditions and interventions

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
Feb 2010 (Type not available)
Primary completion
Oct 2012 (Actual)
Completion
Oct 2012 (Actual)
Last update posted
Oct 9, 2015

2010 – 2012

United States locations

U.S. sites
14
U.S. states
12
U.S. cities
14
Facility City State ZIP Site status
University Of Alabama At Birmingham Birmingham Alabama 35294-0006 —
Alabama Liver & Digestive Specialists (Alds) Montgomery Alabama 36116 —
Florida Hospital Transplant Center Orlando Florida 32804 —
Mercy Medical Center Baltimore Maryland 21202 —
The Research Institute Springfield Massachusetts 01105 —
Umass Memorial Medical Center Worcester Massachusetts 01655 —
James J Peters Vamc The Bronx New York 10468 —
University Of North Carolina, Chapel Hill Chapel Hill North Carolina 27599 —
Healthcare Research Consultants Tulsa Oklahoma 74135-2920 —
Oregon Health Science Univ Portland Oregon 97239 —
Hospital Of The University Of Pennsylvania Philadelphia Pennsylvania 19104 —
Gastro One Germantown Tennessee 38138 —
Metropolitan Research Fairfax Virginia 22031 —
Dean Clinic Madison Wisconsin 53715 —

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 26 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01030432, 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 9, 2015 · Synced Oct 19, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01030432 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →