Efficacy and Safety of MP-424/Peginterferon Alfa-2b/Ribavirin Combination in Treatment-Naïve Patients With Chronic Hepatitis C
Phase 3
Completed
NCT00780416
| Condition | Hepatitis C |
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| Phase | Phase 3 |
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| Sponsor | Tanabe Pharma Corporation |
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| Status | Completed |
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| Enrollment | 189 participants |
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| Interventions | MP-424, Ribavirin, Peginterferon Alfa-2b, Ribavirin, Peginterferon Alfa-2b |
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| Start date | Nov, 2008 |
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| Completion date | Aug, 2010 |
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| Results posted | Aug 20, 2012 |
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Summary
This study will evaluate the efficacy and safety of MP-424 with Peginterferon Alfa-2b (PEG-IFN) and Ribavirin (RBV) in treatment-naïve patients with (Genotype 1) hepatitis C.
The Percentage of Subjects Achieving Undetectable Hepatitis C Virus (HCV) Ribonucleic Acid (RNA) at 24 Weeks After Completion of Drug Administration (SVR, Sustained Viral Response)
After 24 weeks of follow-up · percentage of subjects achieving SVR
| TRV/PEG/RBV | 73.0 percentage of subjects achieving SVR |
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| PEG/RBV | 49.2 percentage of subjects achieving SVR |
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Open in BENITIONS
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