Safety and Efficacy of Daclatasvir (BMS-790052) Plus Standard of Care (Pegylated-interferon Alpha and Ribavirin)
Completed · Phase 2 · Has a placebo group
Conditions studied: Hepatitis C Infection
In brief
The purpose of this study is to identify 1 or more doses of daclatasvir, which when used in combination with pegylated interferon alpha and ribavirin, are safe and demonstrate sufficient anti-hepatitis C virus activity.
Key facts
- Study ID
- NCT00874770
- Run by
- Bristol-Myers Squibb
- People needed
- 74
- Starts
- 2009-06-01
- Expected to finish
- 2011-01-01
- Last updated by the study team
- 2015-10-23
Who can join
Age: 18 and older, up to 70. Sex: any. Healthy volunteers: not accepted.
Where it is running
- Alabama Liver & Digestive Specialists (Alds) — Montgomery, Alabama, United States
- University Of Colorado Denver & Hospital — Aurora, Colorado, United States
- Yale University School Of Medicine — New Haven, Connecticut, United States
- Mercy Medical Center — Baltimore, Maryland, United States
- Llc Dba The Research Institute — Springfield, Massachusetts, United States
- Veterans Affairs Medical Center — The Bronx, New York, United States
- Carolinas Center For Liver Disease — Statesville, North Carolina, United States
- Options Health Research, Llc — Tulsa, Oklahoma, United States
- Healthcare Research Consultants — Tulsa, Oklahoma, United States
- North Texas Research Institute — Arlington, Texas, United States
- Metropolitan Research — Fairfax, Virginia, United States
- Local Institution — Créteil, France
- Local Institution — Paris, France
- Local Institution — Vandœuvre-lès-Nancy, France
Full record on ClinicalTrials.gov
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