A Single Ascending Dose Study of BMS-650032 in HCV Infected Subjects

PHASE1/PHASE2CompletedINTERVENTIONAL
Enrollment

24

Participants

Timeline

Start Date

January 31, 2008

Primary Completion Date

July 31, 2008

Study Completion Date

July 31, 2008

Conditions
Chronic Hepatitis C
Interventions
DRUG

BMS-650032 or Placebo

Oral, Once daily, Single Dose

Trial Locations (5)

21225

Parexel International Corporation, Baltimore

32809

Orlando Clinical Research Center, Orlando

55905

Mayo Clinic, Rochester

78215

Alamo Medical Research, San Antonio

90630

West Coast Clinical Trials, Llc, Cypress

Sponsors
All Listed Sponsors
lead

Bristol-Myers Squibb

INDUSTRY