JPRN-UMIN000006952
Completed
Phase 3
A randomised comparison of safety and efficacy of triple therapy for 12 weeks, followed by 12 or 36 additional weeks of peginterferon alfa 2b and ribavirin in HCV patients - Study of 12 or 36 additional weeks of peginterferon alfa 2b and ribavirin
Hiroshima liver study group0 sites230 target enrollmentDecember 26, 2011
Overview
- Phase
- Phase 3
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- Hiroshima liver study group
- Enrollment
- 230
- Status
- Completed
- Last Updated
- 2 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- Not provided
Exclusion Criteria
- •1\)Transient response to prior treatment 2\)Patients receiving shosaiko\-to 3\)Autoimmune hepatitis 4\)History of hypersensitivity to PEG\-IFN alpha\-2b and telaprevir 5\)History of hypersensitivity to biological products such as vaccine 6\)Decompenstated liver cirrhosis 7\)HCC, malignat tumor 8\)With or with a history of severe psychosis such as severe depression, suicidal ideation or attempt, etc. 9\)Pregnant or lactating women and women who may be pregnant 10\)Judged by investigator not to be appropriate for inclusion in this study
Outcomes
Primary Outcomes
Not specified
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