Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

COMPLETED Phase 3

Study Comparing Daclatasvir (BMS-790052) With Telaprevir Combined With Peginterferon Alfa-2a and Ribavirin in Patients With Chronic Hepatitis C Virus Infection

NCT01492426 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of this study is to compare the effectiveness of BMS-790052 (Daclatasvir) and Telaprevir when given in combination with Peginterferon alfa-2a and Ribavirin in genotype 1b patients

Conditions Studied

Interventions

  • DRUG Ribavirin
  • DRUG Daclatasvir
  • DRUG Peginterferon alfa-2a
  • DRUG Telaprevir

Study Locations (20)

North Carolina

  • University Of North Carolina At Chapel Hill School Of Med — Chapel Hill
  • Carolinas Medical Center — Charlotte
  • Duke University Medical Center — Durham

California

  • Va Long Beach Healthcare System — Long Beach
  • Medical Associates Research Group — San Diego

Georgia

  • Atlanta Medical Center — Atlanta
  • Gastrointestinal Specialists Of Georgia — Marietta

Illinois

  • Northwestern University — Chicago
  • Rush University Medical Center — Chicago

Maryland

  • University Of Maryland — Baltimore
  • Johns Hopkins University — Lutherville

Alabama

  • The Kirklin Clinic — Birmingham

Arizona

  • Mayo Clinic Arizona — Phoenix

Connecticut

  • Yale University School Of Medicine — New Haven

Trial Details

FieldValue
Enrollment Target 605 participants
Start Date 2012-01
Est. Completion 2014-03
Phase Phase 3

Sponsor

Bristol-Myers Squibb

504 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT01492426

The ClinicalTrials.gov registry entry for NCT01492426 describes a study currently listed as completed. It is categorized as Phase 3, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 605 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Bristol-Myers Squibb, which has 504 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Hepatitis C appearing as the primary indexed condition, and to 4 interventions — of which Ribavirin is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT01492426 reports 20 study locations spanning 14 distinct geographic areas — top geographies include North Carolina, California, Georgia. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT01492426 about?

NCT01492426 is a clinical study titled "Study Comparing Daclatasvir (BMS-790052) With Telaprevir Combined With Peginterferon Alfa-2a and Ribavirin in Patients With Chronic Hepatitis C Virus Infection". The purpose of this study is to compare the effectiveness of BMS-790052 (Daclatasvir) and Telaprevir when given in combination with Peginterferon alfa-2a and Ribavirin in genotype 1b patients

What is the current status of trial NCT01492426?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 605 participants. The study started on 2012-01. Estimated completion is 2014-03.

What conditions does trial NCT01492426 study?

This clinical trial studies the following conditions: Hepatitis C. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT01492426?

The interventions under investigation include: Ribavirin (DRUG), Daclatasvir (DRUG), Peginterferon alfa-2a (DRUG), Telaprevir (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT01492426?

This trial is sponsored by Bristol-Myers Squibb, which has 504 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT01492426 being conducted?

This trial has 20 study locations across Alabama, Arizona, California, Connecticut, Florida. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial