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COMPLETED Phase 1

A Single Ascending Dose Study of BMS-791325 in HCV Infected Subjects

NCT00664625 · View on ClinicalTrials.gov ↗

Study Summary

The primary purpose of this study is to evaluate the safety profile and tolerability of single oral doses of BMS-791325 in subjects with chronic hepatitis C infection

Conditions Studied

Interventions

  • DRUG Placebo
  • DRUG BMS-791325

Study Locations (6)

California

  • Advanced Clinical Res Inst — Anaheim
  • West Coast Clinical Trials, Llc — Cypress

Missouri

  • Washington University School Of Medicine — St Louis

Pennsylvania

  • University Of Pennsylvania — Philadelphia

Texas

  • Alamo Medical Research — San Antonio

Buenos Aires

  • Local Institution — Buenos Aires

Trial Details

FieldValue
Enrollment Target 24 participants
Start Date 2008-05
Est. Completion 2009-06
Phase Phase 1

Sponsor

Bristol-Myers Squibb

504 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT00664625

The ClinicalTrials.gov registry entry for NCT00664625 describes a study currently listed as completed. It is categorized as Phase 1, 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 24 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 Chronic Hepatitis C appearing as the primary indexed condition, and to 2 interventions — of which Placebo 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: NCT00664625 reports 6 study locations spanning 5 distinct geographic areas — top geographies include California, Missouri, Pennsylvania. 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 NCT00664625 about?

NCT00664625 is a clinical study titled "A Single Ascending Dose Study of BMS-791325 in HCV Infected Subjects". The primary purpose of this study is to evaluate the safety profile and tolerability of single oral doses of BMS-791325 in subjects with chronic hepatitis C infection

What is the current status of trial NCT00664625?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 24 participants. The study started on 2008-05. Estimated completion is 2009-06.

What conditions does trial NCT00664625 study?

This clinical trial studies the following conditions: Chronic 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 NCT00664625?

The interventions under investigation include: Placebo (DRUG), BMS-791325 (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT00664625?

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 NCT00664625 being conducted?

This trial has 6 study locations across California, Missouri, Pennsylvania, Texas, Buenos Aires. 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