Pegasys® Plus Ribavirin in Thalassemic Patients With Hepatitis C Virus Infection
Primary Purpose
Hepatitis C, Thalassemia
Status
Completed
Phase
Phase 4
Locations
Iran, Islamic Republic of
Study Type
Interventional
Intervention
PEGASYS® (Peginterferon Alfa-2a (40KD)) Plus COPEGUS® (Ribavirin)
Sponsored by
About this trial
This is an interventional treatment trial for Hepatitis C focused on measuring Hepatitis C, Thalassemia, Pegasys, Ribavirin
Eligibility Criteria
Inclusion Criteria:
- HCV RNA positive
- Age older than 12 years
Exclusion Criteria:
- Ongoing pregnancy or breast feeding
- History (Hx) of Hepatocellular Carcinoma (HCC)
- Hx of alcoholic liver disease
- Hx of bleeding from esophageal varices
- Hx of hemochromatosis
- Hx of autoimmune hepatitis
- Hx of Suicidal attempt
- Hx of cerebrovascular dis
- Hx of severe retinopathy
- Hx of severe psoriasis
- Hx of scleroderma
- Hx of metabolic liver disease
- Hx of Systemic Lupus Erythematosus (SLE)
Sites / Locations
- Baqiyatallah Research Center for Gastroenterology and Liver Diseases
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
1
Arm Description
Thalassemic Patients with HCV
Outcomes
Primary Outcome Measures
Early Virologic Response
End of Treatment Response
Sustained Virologic Response
Rapid Virologic Response
Secondary Outcome Measures
Tolerability of drugs for whole therapy period
Biochemical response (ALT)
Laboratory Parameters
Full Information
NCT ID
NCT00707850
First Posted
June 26, 2008
Last Updated
August 30, 2010
Sponsor
Baqiyatallah Medical Sciences University
Collaborators
Baqiyatallah Research Center for Gastroenterology and Liver Diseases, Tehran Hepatitis Center, Guilan University of Medical Sciences, Tabriz Research Center for Gastroenterology and Liver Diseases
1. Study Identification
Unique Protocol Identification Number
NCT00707850
Brief Title
Pegasys® Plus Ribavirin in Thalassemic Patients With Hepatitis C Virus Infection
Official Title
A Study on PEGASYS® (Peginterferon Alfa-2a (40KD)) Plus COPEGUS® (Ribavirin) in Iranian Thalassemic Patients With Chronic Hepatitis C Infection
Study Type
Interventional
2. Study Status
Record Verification Date
September 2009
Overall Recruitment Status
Completed
Study Start Date
May 2007 (undefined)
Primary Completion Date
September 2009 (Actual)
Study Completion Date
September 2009 (Actual)
3. Sponsor/Collaborators
Name of the Sponsor
Baqiyatallah Medical Sciences University
Collaborators
Baqiyatallah Research Center for Gastroenterology and Liver Diseases, Tehran Hepatitis Center, Guilan University of Medical Sciences, Tabriz Research Center for Gastroenterology and Liver Diseases
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Antiviral treatment of HCV in thalassemia has raised concerns of ribavirin-induced hemolysis and increased iron loading. Blood Transfusion in Thalassemic patients are a known high risk for acquiring hepatitis C. The investigators are trying the PEGASYS (Peginterferon alpha-2a(40 KD)) plus Ribavirin in Thalassemic patients with HCV.
Detailed Description
Patients with Thalassemia receive chronic blood transfusions and have an increased prevalence of chronic Hepatitis C virus (HCV) infection, particularly if transfused before HCV serological testing became available. The investigators enrolled 300 patients into the study. The patients received PEGASYS (Peginterferon alpha-2a(40 KD)) 180 microgram per week plus COPEGUS (Ribavirin) 1000 milligram for weight less than or equal 75 kg and 1200 milligram for more than 75 kg for 48 weeks. Follow up period is 6 months after treatment. The patients are visited every 4 weeks with biochemistry lab tests. The patients are checked with quantitative HCV RNA (Ribonucleic Acid) on the third months after initiation of the treatment to assess early virologic response and at the end of the study for complete response rate and on the six month after treatment completion for sustained response rate. The patients with undetectable HCV RNA are considered as responders.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hepatitis C, Thalassemia
Keywords
Hepatitis C, Thalassemia, Pegasys, Ribavirin
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
300 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
1
Arm Type
Experimental
Arm Description
Thalassemic Patients with HCV
Intervention Type
Drug
Intervention Name(s)
PEGASYS® (Peginterferon Alfa-2a (40KD)) Plus COPEGUS® (Ribavirin)
Other Intervention Name(s)
Peginterferon Alfa-2a (40KD) plus COPEGUS
Intervention Description
PEGASYS: 180 microgram per week (Injection) Plus Ribavirin: [=<75 kg: 1000 mg; >75 kg: 1200 mg per day (PO)]
Primary Outcome Measure Information:
Title
Early Virologic Response
Time Frame
After 12 weeks of Treatment
Title
End of Treatment Response
Time Frame
48 Weeks
Title
Sustained Virologic Response
Time Frame
24 weeks after Treatment
Title
Rapid Virologic Response
Time Frame
One month after Treatment
Secondary Outcome Measure Information:
Title
Tolerability of drugs for whole therapy period
Time Frame
During Treatment
Title
Biochemical response (ALT)
Time Frame
End of Treatment AND 24 weeks after Treatment
Title
Laboratory Parameters
Time Frame
During Treatment AND End of treatment
10. Eligibility
Sex
All
Minimum Age & Unit of Time
12 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
HCV RNA positive
Age older than 12 years
Exclusion Criteria:
Ongoing pregnancy or breast feeding
History (Hx) of Hepatocellular Carcinoma (HCC)
Hx of alcoholic liver disease
Hx of bleeding from esophageal varices
Hx of hemochromatosis
Hx of autoimmune hepatitis
Hx of Suicidal attempt
Hx of cerebrovascular dis
Hx of severe retinopathy
Hx of severe psoriasis
Hx of scleroderma
Hx of metabolic liver disease
Hx of Systemic Lupus Erythematosus (SLE)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Seyed-Moayed Alavian, Professor
Organizational Affiliation
Baqiyatallah Research Center for Gastroenterology and Liver Disea
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Seyyed Mohammad Miri, M.D.
Organizational Affiliation
Baqiyatallah Research Center for Gastroenterology and Liver Disea
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Pegah Karimi, M.D.
Organizational Affiliation
Baqiyatallah Research Center for Gastroenterology and Liver Diseases
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Maryam Keshvari, M.D.
Organizational Affiliation
Iranian blood Transfusion Research Center
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Bita Behnava, M.D.
Organizational Affiliation
Baqiyatallah Research Center for Gastroenterology and Liver Diseases
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Mohammad Hossein Somi, M.D.
Organizational Affiliation
Research Center for Gastroenterology and Hepatology, Tabriz University of Medical Sciences, Tabriz
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Fariborz Mansour-Ghanaei, M.D.
Organizational Affiliation
Gastroenterology and Liver Diseases, Gastrointestinal and Liver Diseases Research Center (GLDRC), Guilan University of Medical Sciences, Rasht, Iran
Official's Role
Principal Investigator
Facility Information:
Facility Name
Baqiyatallah Research Center for Gastroenterology and Liver Diseases
City
Tehran
ZIP/Postal Code
14155-3651
Country
Iran, Islamic Republic of
12. IPD Sharing Statement
Citations:
PubMed Identifier
18556414
Citation
Harmatz P, Jonas MM, Kwiatkowski JL, Wright EC, Fischer R, Vichinsky E, Giardina PJ, Neufeld EJ, Porter J, Olivieri N; Thalassemia Clinical Research Network. Safety and efficacy of pegylated interferon alpha-2a and ribavirin for the treatment of hepatitis C in patients with thalassemia. Haematologica. 2008 Aug;93(8):1247-51. doi: 10.3324/haematol.12352. Epub 2008 Jun 12.
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Pegasys® Plus Ribavirin in Thalassemic Patients With Hepatitis C Virus Infection
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