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Phase III Daclatasvir and Sofosbuvir for Genotype 3 Chronic HCV
NCT02032901 · View on ClinicalTrials.gov ↗
Study Summary
To study the combination of Daclatasvir and Sofosbuvir for the treatment of hepatitis C virus (HCV) Genotype 3 infection
Conditions Studied
Interventions
- DRUG Sofosbuvir
- DRUG Daclatasvir
Study Locations (20)
California
- Scripps Clinic — La Jolla
- Peter J Ruane MD Inc — Los Angeles
- National Research Institute — Los Angeles
- Anthony M. Mills MD Inc — Los Angeles
- Huntington Medical Research Institutes — Pasadena
- Precision Research Institute, LLC — San Diego
- Medical Associates Research Group — San Diego
- Quest Clinical Research — San Francisco
Florida
- Midland Florida Clinical Research Center, LLC — DeLand
- University of Florida Hepatology Research — Gainesville
Georgia
- Atlanta Gastroenterology Associates — Atlanta
- Gastrointestinal Specialists Of Georgia — Marietta
Maryland
- Mercy Medical Center, Inc. — Baltimore
- Digestive Disease Associates, P.A. — Baltimore
New York
- North Shore University Hospital — Manhasset
- Premier Medical Group Of The Hudson Valley, Pc — Poughkeepsie
Illinois
- Dupage Medical Group — Downers Grove
Missouri
- Kansas City Research Institute — Kansas City
New Mexico
- Southwest Care Center — Santa Fe
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 173 participants |
| Start Date | 2014-01 |
| Est. Completion | 2014-12 |
| Phase | Phase 3 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02032901
The ClinicalTrials.gov registry entry for NCT02032901 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 173 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 2 interventions — of which Sofosbuvir 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: NCT02032901 reports 20 study locations spanning 9 distinct geographic areas — top geographies include California, Florida, 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 NCT02032901 about?
NCT02032901 is a clinical study titled "Phase III Daclatasvir and Sofosbuvir for Genotype 3 Chronic HCV". To study the combination of Daclatasvir and Sofosbuvir for the treatment of hepatitis C virus (HCV) Genotype 3 infection
What is the current status of trial NCT02032901?
This trial is currently completed. It is a Phase 3 study. The enrollment target is 173 participants. The study started on 2014-01. Estimated completion is 2014-12.
What conditions does trial NCT02032901 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 NCT02032901?
The interventions under investigation include: Sofosbuvir (DRUG), Daclatasvir (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT02032901?
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 NCT02032901 being conducted?
This trial has 20 study locations across California, Florida, Georgia, Illinois, Maryland. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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