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Omega Interferon Alone or in Combination With Ribavirin in Subjects With Hepatitis C

Hepatitis C Clinical Trial

Official title:
Phase 2 Study of Omega Interferon Alone or in Combination With Ribavirin in Subjects With Hepatitis C

Clinical Trial Summary

This study is designed to compare the safety, tolerability and antiviral effects of omega interferon administered alone to omega interferon administered with ribavirin in the treatment of subjects with chronic Hepatitis C virus (HCV) infection.

Clinical Trial Description

Omega interferon is administered subcutaneously daily for up to 48 weeks. ;

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00097045
Study type Interventional
Source Intarcia Therapeutics
Contact
Status Completed
Phase Phase 2
Start date November 2004
Completion date December 2006
View Details
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