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Efficacy and Safety of MP-424, Peginterferon Alfa-2b and Ribavirin in Relapser Genotype 2 Hepatitis C Infected Patients

Phase 3
Completed
Conditions
Chronic Hepatitis C
Interventions
Registration Number
NCT01466192
Lead Sponsor
Mitsubishi Tanabe Pharma Corporation
Brief Summary

This study will evaluate the efficacy and safety of MP-424 with Peginterferon Alfa-2b and Ribavirin (RBV) in patients with genotype 2 hepatitis C, who relapsed after previous treatment.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
108
Inclusion Criteria
  • Genotype 2, chronic hepatitis C
  • Relapsers (patient who relapsed after previous treatment)
  • Able and willing to follow contraception requirements
Exclusion Criteria
  • Cirrhosis of the liver or hepatic failure
  • Hepatitis B surface antigen-positive or HIV antibodies-positive
  • History of, or concurrent hepatocellular carcinoma
  • History of, or concurrent depression, schizophrenia,; or suicide attempt in the past
  • Pregnant, lactating, or suspected pregnant patients, or male patients whose female partner is pregnant

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
MP-424Ribavirin-
MP-424Peginterferon alfa-2b-
Primary Outcome Measures
NameTimeMethod
Undetectable HCV RNA at 24 Weeks After Completion of Drug Administration (SVR, Sustained Viral Response)After 24 weeks of follow-up
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Toranomon Hospital

🇯🇵

Minato-ku, Tokyo, Japan

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