A Randomized Trial of 24-Week Versus 48-Week Courses of Peginterferon Plus Ribavirin for HCV Genotype-6 Patients
Primary Purpose
Chronic Hepatitis C
Status
Completed
Phase
Phase 3
Locations
China
Study Type
Interventional
Intervention
Peginterferon alfa2a
Ribavirin
Peginterferon alfa2a
Ribavirin
Sponsored by
About this trial
This is an interventional treatment trial for Chronic Hepatitis C
Eligibility Criteria
Inclusion Criteria:
- HCV RNA is positive
- Genotype 6
- Treatment naive
- Raised ALT
Exclusion Criteria:
- Active substance abuse
- Poorly controlled psychiatric disease
- HBsAg positive
- Anti-HIV positive
- Suffering from other significant concurrent medical conditions including chronic liver diseases
Sites / Locations
- The Eighth People's Hospital of Guangzhou
- The Third Affliated Hospital of Sun Yat-sen University
- Panyu People's Hospital
- Zhongshan second people's hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
24-Week treatment group
48-Week treatment group
Arm Description
Genotype 6 chronic hepatitis C patients with 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
Genotype 6 chronic hepatitis C patients with 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
Outcomes
Primary Outcome Measures
Sustained virological response (SVR)
Undetectable HCVRNA in serum(<15IU/ml) 24 weeks after the end of treatment
Secondary Outcome Measures
Change in health related quality as measured by short from 36 (SF-36) from baseline to 24 weeks after the end of treatment
Sick leave in patients treated for 24 or 48 weeks treatment
Full Information
NCT ID
NCT01263860
First Posted
December 20, 2010
Last Updated
November 14, 2014
Sponsor
Third Affiliated Hospital, Sun Yat-Sen University
1. Study Identification
Unique Protocol Identification Number
NCT01263860
Brief Title
A Randomized Trial of 24-Week Versus 48-Week Courses of Peginterferon Plus Ribavirin for HCV Genotype-6 Patients
Official Title
A Randomized Trial of 24-Week Versus 48-Week Courses of Peginterferon Plus
Study Type
Interventional
2. Study Status
Record Verification Date
November 2014
Overall Recruitment Status
Completed
Study Start Date
December 2010 (undefined)
Primary Completion Date
June 2014 (Actual)
Study Completion Date
June 2014 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Third Affiliated Hospital, Sun Yat-Sen University
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Patients with HCV genotype 6 infection 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
High rate of infection of Hepatitis C Virus(HCV) Genotype 6 was recently confirmed in Southern China. Recent study implied chronic hepatitis C genotype 6 responds better to the 48-week treatment with pegylated interferon and ribavirin than genotype 1. Approximately 75.7% obtain sustained virological response (HCV RNA undetectable 24 weeks after treatment) to this approach. However, the treatment is associated with many and sometimes serious side effects. In addition, the treatment is costly also in economical terms. Shorter treatment for chronic hepatitis C genotype 6 is necessary to be assessed.
In this randomised,open label,multicenter phase 3 trial with active controls patients are treated with pegylated interferon alfa 2a (180ug/week)and ribavirin(800-1200mg based on weight)for 4 weeks. Those who are HCV RNA negative at week 4 (<50 IU; Cobas Amplicor Monitor Test, Roche Diagnostic) are defined as rapid virological responders and randomised to either an additional 20 or 44 weeks combination treatment. Patients who are HCV RNA positive are all treated for 44 more weeks. The endpoint is sustained virological response defined as undetectable HCV RNA 24 weeks after end of treatment.
Our hypothesis is that there is no important difference in the effect in the two groups.
This is a non-inferiority trial. The smallest difference considered to be clinically important is 15%. Thus to state "non-inferiority" the 95% confidence interval of the observed difference between the groups shall not overlap 10%. Both intention to treat and and per protocol analyses will be published. Conclusion will be conservative and based on the analysis who detect the biggest difference.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Hepatitis C
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
242 (Actual)
8. Arms, Groups, and Interventions
Arm Title
24-Week treatment group
Arm Type
Experimental
Arm Description
Genotype 6 chronic hepatitis C patients with 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
Arm Title
48-Week treatment group
Arm Type
Active Comparator
Arm Description
Genotype 6 chronic hepatitis C patients with 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
Intervention Type
Drug
Intervention Name(s)
Peginterferon alfa2a
Intervention Description
patients receive a dose of 180 µg of PEGASYS once a week for 24 weeks
Intervention Type
Drug
Intervention Name(s)
Ribavirin
Intervention Description
patients receive a dose 800 to 1200 mg of ribavirin once a day(according to weight) for 24 weeks
Intervention Type
Drug
Intervention Name(s)
Peginterferon alfa2a
Intervention Description
patients receive a dose of 180 µg of PEGASYS once a week for 48 weeks
Intervention Type
Drug
Intervention Name(s)
Ribavirin
Intervention Description
patients receive a dose 800 to 1200 mg of ribavirin once a day(according to weight) for 48 weeks
Primary Outcome Measure Information:
Title
Sustained virological response (SVR)
Description
Undetectable HCVRNA in serum(<15IU/ml) 24 weeks after the end of treatment
Time Frame
24 weeks after the end of treatment
Secondary Outcome Measure Information:
Title
Change in health related quality as measured by short from 36 (SF-36) from baseline to 24 weeks after the end of treatment
Time Frame
24 weeks after the end of treatment
Title
Sick leave in patients treated for 24 or 48 weeks treatment
Time Frame
48 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
HCV RNA is positive
Genotype 6
Treatment naive
Raised ALT
Exclusion Criteria:
Active substance abuse
Poorly controlled psychiatric disease
HBsAg positive
Anti-HIV positive
Suffering from other significant concurrent medical conditions including chronic liver diseases
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Gao Zhiliang, Doctor
Organizational Affiliation
The Third Affliated Hospital of Sun Yat-sen University
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Zhao Zhixin, Doctor
Organizational Affiliation
The Third Affliated Hospital of Sun Yat-sen University
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Zhang Xiaohong, Doctor
Organizational Affiliation
The Third Affliated Hospital of Sun Yat-sen University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Xu Min, Doctor
Organizational Affiliation
The Eighth People's Hospital of Guangzhou
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Wei min, Doctor
Organizational Affiliation
Zhongshan second people's hospital
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Huang mingshou, Bachelor
Organizational Affiliation
Panyu People's Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
The Eighth People's Hospital of Guangzhou
City
Guangzhou
State/Province
Guangdong
ZIP/Postal Code
510060
Country
China
Facility Name
The Third Affliated Hospital of Sun Yat-sen University
City
Guangzhou
State/Province
Guangdong
ZIP/Postal Code
510630
Country
China
Facility Name
Panyu People's Hospital
City
Guangzhou
State/Province
Guangdong
Country
China
Facility Name
Zhongshan second people's hospital
City
Zhongshan
State/Province
Guangdong
Country
China
12. IPD Sharing Statement
Citations:
PubMed Identifier
26509605
Citation
Cai Q, Zhang X, Lin C, Shao X, Guan Y, Deng H, Wei M, Huang M, Ren Z, Lu L, Mei Y, Xu M, Zhu J, Shi H, Lin G, Liu Y, Hu F, Luo Q, Lan Y, Guo F, Zhao Z, Gao Z. 24 versus 48 Weeks of Peginterferon Plus Ribavirin in Hepatitis C Virus Genotype 6 Chronically Infected Patients with a Rapid Virological Response: A Non-Inferiority Randomized Controlled Trial. PLoS One. 2015 Oct 28;10(10):e0140853. doi: 10.1371/journal.pone.0140853. eCollection 2015.
Results Reference
derived
Learn more about this trial
A Randomized Trial of 24-Week Versus 48-Week Courses of Peginterferon Plus Ribavirin for HCV Genotype-6 Patients
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