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A Randomized Trial of 24-Week Versus 48-Week Courses of Peginterferon Plus Ribavirin for Patients With Genotype 1 Hepatitis C and IL28B CC Polymorphism

Phase 3
Conditions
Chronic Hepatitis C
Interventions
Registration Number
NCT01441804
Lead Sponsor
Third Affiliated Hospital, Sun Yat-Sen University
Brief Summary

Patients with HCV genotype 1 and IL28B CC Polymorphism who have a rapid virological response to treatment are randomised to either 24 or 48 weeks HCV treatment. Our hypothesis is that there is no important difference in effect between the two treatment effect.

Detailed Description

Not available

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
200
Inclusion Criteria
  • Age > 18 years
  • Serum Hepatitis C RNA > 10,000IU/mL
  • Hepatitis C virus genotype 1
  • IL28B CC polymorphism
Exclusion Criteria
  • Previous treatment for chronic Hepatitis C

  • clinical or biological evidence of acute hepatitis, including serum ALT or AST > 300U/ml

  • HIV antibody positive, hepatitis b surface antigen positive or known diagnosis of other chronic liver disease

  • Contraindications to PR-based treatment:

    • Uncontrolled psychiatric illness
    • Active substance dependency
    • Known autoimmune disorder
    • Untreated thyroid disease
    • Uncontrolled seizure disorder
    • Pregnancy, lactation or inability to maintain contraception
    • Chronic kidney disease w/ estimated GFR< 60
    • ANC<1.5/nl, Hb<12g/dl, or platelets<75/nl
  • Clinical or biochemical evidence of decompensated liver disease including:

    • History of encephalopathy
    • Ascites
    • Variceal bleeding
    • Bilirubin > 3g/dl or INR > 1.5
    • Life threatening disorder with expected median survival less than 5 years
    • Inability to comply with drug regimens or testing schedule required for study

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
24-Week treatment groupPeginterferon alfa2aGenotype 1 chronic hepatitis C patients with IL28B CC Polymorphism and rapid virological response(undetectable HCV RNA at weeks 4) in this group will be treated with Peginterferon alfa-2a plus ribavirin for an additional 20 weeks
48-Week treatment groupPeginterferon alfa2aGenotype 1 chronic hepatitis C patients with IL28B CC Polymorphism and rapid virological response(undetectable HCV RNA at weeks 4) in this group will be treated with Peginterferon alfa-2a plus ribavirin for an additional 44 weeks
24-Week treatment groupRibavirinGenotype 1 chronic hepatitis C patients with IL28B CC Polymorphism and rapid virological response(undetectable HCV RNA at weeks 4) in this group will be treated with Peginterferon alfa-2a plus ribavirin for an additional 20 weeks
48-Week treatment groupRibavirinGenotype 1 chronic hepatitis C patients with IL28B CC Polymorphism and rapid virological response(undetectable HCV RNA at weeks 4) in this group will be treated with Peginterferon alfa-2a plus ribavirin for an additional 44 weeks
Primary Outcome Measures
NameTimeMethod
Sustained virological response (SVR)24 weeks after the end of treatment

Undetectable HCVRNA in serum(\<15IU/ml) 24 weeks after the end of treatment

Secondary Outcome Measures
NameTimeMethod
Sick leave in patients treated for 24 or 48 weeks treatment48 weeks
Change in health related quality as measured by short from 36 (SF-36) from baseline to 24 weeks after the end of treatmentbaseline, 24 weeks after the end of treatment

Trial Locations

Locations (4)

Zhongshan second people's hospital

🇨🇳

Zhongshan, Guangdong, China

The Third Affliated Hospital of Sun Yat-sen University

🇨🇳

Guangzhou, Guangdong, China

Panyu People's Hospital

🇨🇳

Guangzhou, Guangdong, China

The Eighth People's Hospital of Guangzhou

🇨🇳

Guangzhou, Guangdong, China

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