Adaptive Phase I HCV Study With Nucleoside Analogue, in Combination With Interferon and Ribavirin

PHASE1/PHASE2CompletedINTERVENTIONAL
Enrollment

75

Participants

Timeline

Start Date

October 31, 2006

Primary Completion Date

September 30, 2008

Study Completion Date

September 30, 2008

Conditions
Healthy VolunteersHepatitis C Virus
Interventions
DRUG

RO5024048

Trial Locations (9)

19104

Hospital of the University of Pennsylvania, Philadelphia

27710

Duke Clinical Research Institute, Durham

32610

University of Florida, Gainesville

32803

Orlando Immunology Center, Orlando

52242

University of Iowa, Iowa City

80045

University of Colorado Health Sciences Center, Aurora

94115

Quest Clinical Research, San Francisco

Unknown

Auckland Clinical Studies Limited, Grafton

00909

Fundacion de Investigacion de Diego, Santurce

Sponsors

Lead Sponsor

All Listed Sponsors
collaborator

Hoffmann-La Roche

INDUSTRY

lead

Pharmasset

INDUSTRY

NCT00382798 - Adaptive Phase I HCV Study With Nucleoside Analogue, in Combination With Interferon and Ribavirin | Biotech Hunter | Biotech Hunter