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14 vs 24 Weeks HCV Treatment to Genotype 2/3 Patients With Rapid Virological Response

Primary Purpose

Hepatitis C Virus Infection

Status
Completed
Phase
Phase 3
Locations
Norway
Study Type
Interventional
Intervention
Pegylated Interferon alfa 2b and ribavirin
Sponsored by
Ullevaal University Hospital
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Hepatitis C Virus Infection focused on measuring Interferon, Pegylated interferon, Pegylated interferon alfa 2b, Hepatitis C, Genotype 2, Genotype 3, Rapid virological response, Short treatment, 14 weeks treatment, health related quality of life, sick leave, Injecting drug use

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)MaleDoes not accept healthy volunteers

Inclusion Criteria: HCV RNA positive Genotype 2 or 3 Treatment naive Raised ALT - Exclusion Criteria: Active substance abuse Poorly controlled psychiatric disease Decompensated cirrhosis HBsAg positive Anti-HIV positive Suffering from other significant concurrent medical conditions including chronic liver diseases -

Sites / Locations

  • Ullevaal University Hospital

Outcomes

Primary Outcome Measures

Sustained virological response (SVR) =HCV RNA negativity (<20 IU/ml) six months after end of treatment.

Secondary Outcome Measures

Change in health related quality as measured by short from 36 (SF-36) from baseline to 6 months after end of treatment.
Sick leave in patients treated for 14 or 24 weeks treatment

Full Information

First Posted
March 27, 2006
Last Updated
July 3, 2011
Sponsor
Ullevaal University Hospital
Collaborators
Schering-Plough
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1. Study Identification

Unique Protocol Identification Number
NCT00308048
Brief Title
14 vs 24 Weeks HCV Treatment to Genotype 2/3 Patients With Rapid Virological Response
Official Title
14 vs 24 Weeks HCV Treatment to Genotype 2/3 Patients With Rapid Virological Response
Study Type
Interventional

2. Study Status

Record Verification Date
March 2006
Overall Recruitment Status
Completed
Study Start Date
March 2004 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
September 2006 (undefined)

3. Sponsor/Collaborators

Name of the Sponsor
Ullevaal University Hospital
Collaborators
Schering-Plough

4. Oversight

5. Study Description

Brief Summary
Patients with HCV genotype 2 or 3 infection who have a rapid virological response to treatment are randomised to either 14 or 24 weeks HCV treatment. Our hypothesis is that there is no important difference in effect between the two treatment effect.
Detailed Description
Patients with HCV genotype 2 or 3 infection are currently recommended 6 months treatment with pegylated interferon alfa (2a or 2b) and ribavirin.Approximately 80% obtain sustained virological response (HCV RNA undetectable 6 months 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 econimical terms. Increasing the treatment duration beyond 6 months does not increase the response rate. Shorter treatment has only been assessed in small trials, but the results have been encouraging. In this randomised, open label,multicenter phase 3 trial with acitive controls patients are treated with pegylated interferon alfa 2a (PegIntron (R), Schering Plough NJ)(1,5 mcg/kg)and ribavirin (Rebetol (R), Schering Plough, NJ) (800-1400mg 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 10 or 20 weeks combination treatment. Patients who are HCV RNA positive are all treated for 20 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 10%. 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
Hepatitis C Virus Infection
Keywords
Interferon, Pegylated interferon, Pegylated interferon alfa 2b, Hepatitis C, Genotype 2, Genotype 3, Rapid virological response, Short treatment, 14 weeks treatment, health related quality of life, sick leave, Injecting drug use

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
435 (false)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
Pegylated Interferon alfa 2b and ribavirin
Primary Outcome Measure Information:
Title
Sustained virological response (SVR) =HCV RNA negativity (<20 IU/ml) six months after end of treatment.
Secondary Outcome Measure Information:
Title
Change in health related quality as measured by short from 36 (SF-36) from baseline to 6 months after end of treatment.
Title
Sick leave in patients treated for 14 or 24 weeks treatment

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: HCV RNA positive Genotype 2 or 3 Treatment naive Raised ALT - Exclusion Criteria: Active substance abuse Poorly controlled psychiatric disease Decompensated cirrhosis 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
Olav Dalgard, MD PhD
Organizational Affiliation
Ullevaal University Hospital, Oslo, Norway
Official's Role
Principal Investigator
Facility Information:
Facility Name
Ullevaal University Hospital
City
Oslo
ZIP/Postal Code
0407
Country
Norway

12. IPD Sharing Statement

Citations:
PubMed Identifier
15558712
Citation
Dalgard O, Bjoro K, Hellum KB, Myrvang B, Ritland S, Skaug K, Raknerud N, Bell H. Treatment with pegylated interferon and ribavarin in HCV infection with genotype 2 or 3 for 14 weeks: a pilot study. Hepatology. 2004 Dec;40(6):1260-5. doi: 10.1002/hep.20467.
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14 vs 24 Weeks HCV Treatment to Genotype 2/3 Patients With Rapid Virological Response

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