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A Study to Evaluate the Safety and Efficacy of Celgosivir and Peginterferon Alfa-2b, With or Without Ribavirin, in Patients With Chronic Hepatitis C Genotype 1 Infection

Phase 2
Completed
Conditions
Hepatitis C, Chronic
Registration Number
NCT00217139
Lead Sponsor
BioWest Therapeutics Inc
Brief Summary

The objective of the study is to evaluate the safety and efficacy of celgosivir plus peginterferon alfa-2b, with or without ribavirin, for 12 weeks in patients with chronic hepatitis C genotype 1 infection.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
60
Inclusion Criteria
  • 18-65 years of age, inclusive
  • primary diagnosis of chronic HCV infection
  • non-responders to previous pegylated interferon-based therapy
Exclusion Criteria
  • patients naive to interferon-based therapy for chronic HCV infection

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Safety analysis
HCV viral load
Secondary Outcome Measures
NameTimeMethod
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