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Interferon Gamma With Peg-Interferon Alpha 2a and Ribavirin in Non Responders Patients With Chronic Hepatitis C

Primary Purpose

Hepatitis C, Chronic

Status
Completed
Phase
Phase 2
Locations
France
Study Type
Interventional
Intervention
Peg-interferon alpha 2a (drug)
Ribavirin (drug)
Interferon gamma (drug)
Sponsored by
French National Agency for Research on AIDS and Viral Hepatitis
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Hepatitis C, Chronic focused on measuring Hepatitis C, Chronic, Interferon Alfa-2a, Ribavirin, Interferon-gamma, Recombinant

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Positive anti-HCV antibodies Positive HCV RNA (quantitative method) Previous treatment with Peg-interferon alpha 2b 1.0 to 1.5 micro g/kg (during at least 12 weeks) with ribavirin (at least 800 mg/day during at least 12 weeks),stopped since at least 3 months Without lower dosage during previous treatment Non responder to the previous treatment with Peg-interferon alpha 2b and ribavirin, with detectable HCV RNA at W24 or decrease of less than 2 log10 copies/ml at W12 or decrease greater than 2 log10 but detectable HCV RNA Metavir over F2 on the most recent biopsy ALT increase over normal value twice during last 6 months Exclusion Criteria: HIV infection Psychiatric pathology Alcool consummation Cirrhosis Pregnancy or plan of pregnancy Breastfeeding

Sites / Locations

  • Hopital Haut Leveque Service d'Hepato-Gastro-Enterologie
  • Hôpital du Haut-Levêque

Outcomes

Primary Outcome Measures

Virological response as defined by an HCV RNA measure non detectable at W28 with qualitative PCR (centralized measure)

Secondary Outcome Measures

Virological response at W72
Biochemical response at W72 (ALT below normal value)
Quality of life
Immunologic response (CD4 and CD8 HCV specific)
Safety

Full Information

First Posted
September 7, 2005
Last Updated
August 29, 2007
Sponsor
French National Agency for Research on AIDS and Viral Hepatitis
Collaborators
InterMune, Hoffmann-La Roche
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1. Study Identification

Unique Protocol Identification Number
NCT00148863
Brief Title
Interferon Gamma With Peg-Interferon Alpha 2a and Ribavirin in Non Responders Patients With Chronic Hepatitis C
Official Title
Pilot Study on Interferon Gamma in Association With Peg-Interferon Alpha 2a and Ribavirin Among Patients With a Chronic Hepatitis C and Non Responders to the Association of Peg-Interferon Alpha 2b or 2a and Ribavirin ANRS HC16 Gammatri
Study Type
Interventional

2. Study Status

Record Verification Date
August 2007
Overall Recruitment Status
Completed
Study Start Date
June 2004 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
August 2007 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
French National Agency for Research on AIDS and Viral Hepatitis
Collaborators
InterMune, Hoffmann-La Roche

4. Oversight

5. Study Description

Brief Summary
Viral hepatitis C is treated with peg-interferon alpha 2a/2b and ribavirin. There is no treatment recommended for non responders patients. This study will evaluate the efficacy, after a second treatment with peg-interferon alpha 2a and ribavirin for 12 Weeks of the addition of interferon gamma in non responders patients
Detailed Description
Viral hepatitis C is treated with peg-interferon alpha 2a/2b and ribavirin for 24 Weeks. In many patients, there is no efficacy of this treatment on hepatitis C, and there is no treatment recommended for them. Interferon gamma has anti-infectious and anti-fibrosis activity. This study will evaluate the effect, after a second treatment with peg-interferon alpha 2a and ribavirin for 12 Weeks, of the addition of interferon gamma in non responders patients. 65 patients will be included in order to include 27 patients who are non responders after 12 weeks of a second treatment and are eligible to receive interferon gamma. Patients will then receive peg-interferon alpha 2a (180 micro g once a week, by injection), ribavirin (1,000 to 1,200 mg per day, according to weight) and interferon gamma (100 micro g thrice a week, by injection) during 8 months

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hepatitis C, Chronic
Keywords
Hepatitis C, Chronic, Interferon Alfa-2a, Ribavirin, Interferon-gamma, Recombinant

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
65 (false)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
Peg-interferon alpha 2a (drug)
Intervention Type
Drug
Intervention Name(s)
Ribavirin (drug)
Intervention Type
Drug
Intervention Name(s)
Interferon gamma (drug)
Primary Outcome Measure Information:
Title
Virological response as defined by an HCV RNA measure non detectable at W28 with qualitative PCR (centralized measure)
Secondary Outcome Measure Information:
Title
Virological response at W72
Title
Biochemical response at W72 (ALT below normal value)
Title
Quality of life
Title
Immunologic response (CD4 and CD8 HCV specific)
Title
Safety

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Positive anti-HCV antibodies Positive HCV RNA (quantitative method) Previous treatment with Peg-interferon alpha 2b 1.0 to 1.5 micro g/kg (during at least 12 weeks) with ribavirin (at least 800 mg/day during at least 12 weeks),stopped since at least 3 months Without lower dosage during previous treatment Non responder to the previous treatment with Peg-interferon alpha 2b and ribavirin, with detectable HCV RNA at W24 or decrease of less than 2 log10 copies/ml at W12 or decrease greater than 2 log10 but detectable HCV RNA Metavir over F2 on the most recent biopsy ALT increase over normal value twice during last 6 months Exclusion Criteria: HIV infection Psychiatric pathology Alcool consummation Cirrhosis Pregnancy or plan of pregnancy Breastfeeding
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Patrice Couzigou, MD, PhD
Organizational Affiliation
Hôpital du Haut-Lévêque, Pessac, France
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Geneviève Chêne, MD, PhD
Organizational Affiliation
INSERM U593, Bordeaux, France
Official's Role
Study Director
Facility Information:
Facility Name
Hopital Haut Leveque Service d'Hepato-Gastro-Enterologie
City
Pessac
ZIP/Postal Code
33604
Country
France
Facility Name
Hôpital du Haut-Levêque
City
Pessac
ZIP/Postal Code
33604
Country
France

12. IPD Sharing Statement

Citations:
PubMed Identifier
23190183
Citation
Couzigou P, Perusat S, Bourliere M, Trimoulet P, Poynard T, Leroy V, Marcellin P, Foucher J, Bronowicki JP, Chene G; ANRS HC16 GAMMATRI Trial Group. Interferon-gamma with peginterferon alpha-2a and ribavirin in nonresponder patients with chronic hepatitis C (ANRS HC16 GAMMATRI). J Gastroenterol Hepatol. 2013 Feb;28(2):329-34. doi: 10.1111/jgh.12060.
Results Reference
derived

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Interferon Gamma With Peg-Interferon Alpha 2a and Ribavirin in Non Responders Patients With Chronic Hepatitis C

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