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Chronic Hepatitis C Treatment by Pegylated Interferon and Ribavirin in Naive Egyptian Patients (ANRS 1211)

Primary Purpose

Chronic Hepatitis C

Status
Completed
Phase
Phase 3
Locations
Egypt
Study Type
Interventional
Intervention
pegylated interferon alpha2a
ribavirin
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 Chronic Hepatitis C focused on measuring Chronic Hepatitis C, Genotype 4, Pegylated Interferon, Ribavirin, Egypt

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: HCV antibodies using a third generation test HCV RNA positive by PCR Liver biopsy in the past 18 months with METAVIR score over A2 and over or equal to F1, or over or equal A1 and over F2 ALT over 1.5 time the normal range in the 24 weeks prior to inclusion (Week-28; W-2); Patients never treated with ribavirin, IFNalpha or PEG-IFNalpha Normal albumin Prothrombin time over or equal to 60 percent Normal bilirubin Alpha-foeto-protein under or equal to 3 times the normal range for the laboratory HBs antigen negative Two negative Kato test (for S.mansoni) three days apart Hemoglobin over or equal 11g/dl, Leucocytes over or equal 3000/mm3 Neutrophils over or equal 1500/mm3 Platelets over or equal 100 000/mm3 Blood creatinin over or equal 150 micromol/l Normal TSH Anti-nuclear antibodies under 1/160 Fasting blood sugar between 70-115mg/dl (if glucose intolerance or diabetes: HbA1C <= 8,5%) Normal ophthalmologic examination in patients with history of blood pressure and/or diabetes Effective contraception during the treatment period No breastfeeding during the study period. Signed informed consent Exclusion Criteria: Co-infection with hepatitis B (positive HBs antigen) Hemochromatosis Alpha-1 anti-trypsin deficiency Wilson disease Alcoholism-related liver disease Gilbert disease Alcohol intake over 50g/day for males and 40 g/day for females Ongoing intravenous drug use Aggravated liver cirrhosis (history or presence of ascitis, oesophageal varicosis, liver encephalopathy) Hepatocellular carcinoma Psychiatric disease: history of severe nervous breakdown or severe psychiatric diseases such as major psychosis, suicidal ideas, suicide attempts… Epilepsy Auto-immune disease Heart disease in the six months preceding enrolment - patients with significant changes at EKG Uncontrolled diabetes Chronic respiratory insufficiency with hypoxemia <10 kPa Medical or surgical condition, non-stabilised, with life expectancy lower than two years. Pregnancy or breastfeeding

Sites / Locations

  • Ismail Sallam hospital
  • National Hepatology and Tropical Medicine Research Institute

Outcomes

Primary Outcome Measures

- Disappearance of HCV RNA by qualitative PCR 24 weeks after the end of treatment

Secondary Outcome Measures

Evaluation of HCV RNA at 12 and 24 weeks
changes in HCV RNA load during treatment
Normalization of ALT during treatment and 24 weeks after the end of treatment
Study of side effects
Histological changes 24 weeks after the end of treatment (decrease by at least 1 point of the Metavir score)

Full Information

First Posted
September 8, 2005
Last Updated
April 23, 2007
Sponsor
French National Agency for Research on AIDS and Viral Hepatitis
Collaborators
Hoffmann-La Roche
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1. Study Identification

Unique Protocol Identification Number
NCT00158496
Brief Title
Chronic Hepatitis C Treatment by Pegylated Interferon and Ribavirin in Naive Egyptian Patients (ANRS 1211)
Official Title
Clinical Trial of the Efficacy of the Combination of Pegylated Interferon (PEG-IFNα-2a) Plus Ribavirin in Egyptian Patients With Untreated Chronic Hepatitis C
Study Type
Interventional

2. Study Status

Record Verification Date
April 2007
Overall Recruitment Status
Completed
Study Start Date
August 2002 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
January 2005 (Actual)

3. Sponsor/Collaborators

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

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Chronic hepatitis C is a liver disease related to a virus: hepatitis C virus (HCV). The type of HCV present in Egypt (genotype 4), has the reputation to respond poorly to Interferon treatment at the chronic stage. Pegylated Interferon is a new form of Interferon that stays in the body for longer time and allows the patient to take less injection per week. It has proved to be more effective than standard Interferon. The combination of two drugs, Interferon and Ribavirin, is considered to be the best treatment available for chronic hepatitis C.
Detailed Description
Egypt is the country with the highest HCV prevalence worldwide, and the number of infected Egyptians is estimated around 8 million. The HCV genotype circulating in Egypt is genotype 4. This genotype has the reputation, based on the few available data, to respond poorly to treatment. This study will estimate the safety and efficacy of the combination of peg-IFNα-2a plus Ribavirin, in Egyptian patients with chronic hepatitis C. This treatment has been chosen based on its better expected efficacy compared to pegylated interferon alone. The primary objective of the study is to assess the efficacy and tolerance of the combination of pegylated interferon (peg-IFNα-2a) plus ribavirin in Egyptian patients with chronic hepatitis C and with no prior treatment for HCV. Methods: Open trial. Follow-up duration: 72 weeks. Enrolment duration: 18 months. Total trial duration: 3 years and a half, including trial analysis (carried out in the 6 months following the follow-up completion of the last patient). Total number of patients: 100. Precision around the expected efficacy rate (40% in intention-to-treat analysis): 9.6%. Treatment strategy: Peg-IFNα-2a 180microg/week for 48 weeks, Ribavirin at least 11 mg/kg/day for 48 weeks Main inclusion criteria: HCV RNA positive by PCR; METAVIR score : >A2 and >= F1 or >= A1 and > F2; ALAT over 1.5*N; no prior treatment with IFNalpha, PEG-IFNalpha and ribavirin Main exclusion criteria : Liver disease other than hepatitis C; advanced liver disease; negative HCV RNA. Patient from a cohort follow-up conducted in a village in rural Egypt with High HCV prevalence (Menoufia governorate) will be proposed to participate in the trial. Pre-enrolment investigations, liver biopsy, and patients follow-up will be carried out at a local hospital. Blood test analyses will be carried out under the responsibility of Hepatitis Virology Reference Laboratory at the National Hepatology and Tropical Medicine Institute, Cairo; trial monitoring will be carried out by the Department of Community Medicine of Ain Shams; methodological assistance from the "Unite des Maladies Emergentes" at Pasteur Institute and INSERM U444, Paris. Treatment for patients with HCV RNA by qualitative PCR still positive after 24 weeks of the combination Peg-IFNα-2a with ribavirin, will be stopped.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Hepatitis C
Keywords
Chronic Hepatitis C, Genotype 4, Pegylated Interferon, Ribavirin, Egypt

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
100 (false)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
pegylated interferon alpha2a
Intervention Type
Drug
Intervention Name(s)
ribavirin
Primary Outcome Measure Information:
Title
- Disappearance of HCV RNA by qualitative PCR 24 weeks after the end of treatment
Secondary Outcome Measure Information:
Title
Evaluation of HCV RNA at 12 and 24 weeks
Title
changes in HCV RNA load during treatment
Title
Normalization of ALT during treatment and 24 weeks after the end of treatment
Title
Study of side effects
Title
Histological changes 24 weeks after the end of treatment (decrease by at least 1 point of the Metavir score)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: HCV antibodies using a third generation test HCV RNA positive by PCR Liver biopsy in the past 18 months with METAVIR score over A2 and over or equal to F1, or over or equal A1 and over F2 ALT over 1.5 time the normal range in the 24 weeks prior to inclusion (Week-28; W-2); Patients never treated with ribavirin, IFNalpha or PEG-IFNalpha Normal albumin Prothrombin time over or equal to 60 percent Normal bilirubin Alpha-foeto-protein under or equal to 3 times the normal range for the laboratory HBs antigen negative Two negative Kato test (for S.mansoni) three days apart Hemoglobin over or equal 11g/dl, Leucocytes over or equal 3000/mm3 Neutrophils over or equal 1500/mm3 Platelets over or equal 100 000/mm3 Blood creatinin over or equal 150 micromol/l Normal TSH Anti-nuclear antibodies under 1/160 Fasting blood sugar between 70-115mg/dl (if glucose intolerance or diabetes: HbA1C <= 8,5%) Normal ophthalmologic examination in patients with history of blood pressure and/or diabetes Effective contraception during the treatment period No breastfeeding during the study period. Signed informed consent Exclusion Criteria: Co-infection with hepatitis B (positive HBs antigen) Hemochromatosis Alpha-1 anti-trypsin deficiency Wilson disease Alcoholism-related liver disease Gilbert disease Alcohol intake over 50g/day for males and 40 g/day for females Ongoing intravenous drug use Aggravated liver cirrhosis (history or presence of ascitis, oesophageal varicosis, liver encephalopathy) Hepatocellular carcinoma Psychiatric disease: history of severe nervous breakdown or severe psychiatric diseases such as major psychosis, suicidal ideas, suicide attempts… Epilepsy Auto-immune disease Heart disease in the six months preceding enrolment - patients with significant changes at EKG Uncontrolled diabetes Chronic respiratory insufficiency with hypoxemia <10 kPa Medical or surgical condition, non-stabilised, with life expectancy lower than two years. Pregnancy or breastfeeding
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Arnaud Fontanet
Organizational Affiliation
Institut Pasteur de Paris
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Mostafa K Mohamed
Organizational Affiliation
National Hepatology and Tropical Medicine Research Institute
Official's Role
Principal Investigator
Facility Information:
Facility Name
Ismail Sallam hospital
City
Zawiat Razin
State/Province
Menoufia
Country
Egypt
Facility Name
National Hepatology and Tropical Medicine Research Institute
City
Cairo
Country
Egypt

12. IPD Sharing Statement

Citations:
PubMed Identifier
16956918
Citation
Marzouk D, Sass J, Bakr I, El Hosseiny M, Abdel-Hamid M, Rekacewicz C, Chaturvedi N, Mohamed MK, Fontanet A. Metabolic and cardiovascular risk profiles and hepatitis C virus infection in rural Egypt. Gut. 2007 Aug;56(8):1105-10. doi: 10.1136/gut.2006.091983. Epub 2006 Sep 6.
Results Reference
background
PubMed Identifier
16847958
Citation
Mohamed MK, Bakr I, El-Hoseiny M, Arafa N, Hassan A, Ismail S, Anwar M, Attala M, Rekacewicz C, Zalata K, Abdel-Hamid M, Esmat G, Fontanet A. HCV-related morbidity in a rural community of Egypt. J Med Virol. 2006 Sep;78(9):1185-9. doi: 10.1002/jmv.20679.
Results Reference
background
PubMed Identifier
16434426
Citation
Bakr I, Rekacewicz C, El Hosseiny M, Ismail S, El Daly M, El-Kafrawy S, Esmat G, Hamid MA, Mohamed MK, Fontanet A. Higher clearance of hepatitis C virus infection in females compared with males. Gut. 2006 Aug;55(8):1183-7. doi: 10.1136/gut.2005.078147. Epub 2006 Jan 24.
Results Reference
background
PubMed Identifier
16019104
Citation
Arafa N, El Hoseiny M, Rekacewicz C, Bakr I, El-Kafrawy S, El Daly M, Aoun S, Marzouk D, Mohamed MK, Fontanet A. Changing pattern of hepatitis C virus spread in rural areas of Egypt. J Hepatol. 2005 Sep;43(3):418-24. doi: 10.1016/j.jhep.2005.03.021.
Results Reference
background
Links:
URL
http://www.anrs.fr
Description
Sponsor web page - information in french and english

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Chronic Hepatitis C Treatment by Pegylated Interferon and Ribavirin in Naive Egyptian Patients (ANRS 1211)

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