Ph IIA Study (SOC +/- NS5B)

PHASE2CompletedINTERVENTIONAL
Enrollment

39

Participants

Timeline

Start Date

October 31, 2010

Primary Completion Date

June 30, 2011

Study Completion Date

November 30, 2012

Conditions
Hepatitis C Virus
Interventions
DRUG

BMS-791325

Tablets, Oral, 75 mg, twice daily, 4-48 weeks depending on response

DRUG

BMS-791325

Tablets, Oral, 150 mg, twice daily, 4-48 weeks depending on response

DRUG

Placebo

Tablets, Oral, 0 mg, twice daily, 4-48 weeks depending on response

DRUG

Peg-interferon alfa-2a

Syringe, Subcutaneous Injection, 180 µg, once weekly, 4-48 weeks depending on response

DRUG

Ribavirin

Tablets, Oral, 1000 or 1200 mg based on weight, twice daily, 4-48 weeks depending on response

Trial Locations (10)

21202

Mercy Medical Center, Baltimore

21229

Digestive Disease Associates, P.A., Baltimore

22031

Metropolitan Research, Fairfax

28207

Charlotte Gastroenterology & Hepatology, Pllc, Charlotte

60153

Loyola University Medical Center, Maywood

74104

Options Health Research, Llc, Tulsa

76012

The North Texas Research Institute, Arlington

78215

Alamo Medical Research, San Antonio

92801

Advanced Clinical Research Institute, Anaheim

01107

Claudia T. Martorell, Md, Llc, Springfield

Sponsors
All Listed Sponsors
lead

Bristol-Myers Squibb

INDUSTRY