Combination Therapy With Pegylated Interferon and Ribavirin in Patients With Chronic Hepatitis C Genotype 2 or 3 Infection Who Previously Have Relapsed After Therapy With Pegylated Interferon and Ribavirin

Chronic Hepatitis C Clinical Trial

— RelapC  

Official title:

An Open-label Multicenter Study Evaluating the Efficacy and Safety of 24 or 48 Weeks Pegylated Interferon Alfa-2a 40 kD (PEGASYS) Combination Therapy With Ribavirin (Copegus) in Patients With Chronic Hepatitis C Genotype 2 or 3 Infection Who Previously Have Relapsed After a Minimum of 12 Weeks and a Maximum of 24 Weeks of Therapy With Pegylated Interferon and Ribavirin

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT00641654
• Other study ID #: EudractCT 2006-003409-18
• Status: Terminated
• Phase: Phase 4
• First received: March 17, 2008
• Last updated: August 29, 2012
• Start date: January 2007
• Est. completion date: December 2009

Study information

• Verified date: March 2012
• Source: Göteborg University
• Contact: n/a
• Is FDA regulated: No
• Health authority: Sweden: Medical Products Agency
• Study type: Interventional

Clinical Trial Summary

To evaluate the efficacy of pegylated interferon alfa-2a 40 kD (PEGASYS) combination therapy with ribavirin (Copegus)given for 24 or 48 weeks in patients with chronic hepatitis C (CHC) virus infection genotype 2 or 3 who responded during (i.e. had HCV-RNA <50 IU/mL at the end of previous therapy), but relapsed after (i.e. had detectable HCV-RNA after the end of prior treatment) previous therapy with pegylated interferon and ribavirin given for at least 12 weeks and at most 24 weeks.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 75
• Est. completion date: December 2009
• Est. primary completion date: December 2009
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Male and female patients = 18 years of age

• Serologic evidence of chronic hepatitis C infection by an anti-HCV antibody test

• Serum HCV-RNA = 15 IU/mL. HCV genotype 2 or/and 3 infection confirmed within the past 6 months preceding the initiation of test drug dosing. The HCV genotype must have been reconfirmed after the termination of the previous treatment period

• Previous relapse (i.e. HCV-RNA < 50 IU/mL at end of previous therapy) after one treatment period with pegylated interferon alfa-2a or alfa-2b combination therapy with ribavirin for at least 12 weeks and at most 24 weeks

• A minimum of 24 weeks must have elapsed since the last dose of pegylated interferon or ribavirin in the previous treatment period before the patients can be included in this study

• Compensated liver disease (Child-Pugh Grade A clinical classification)

• Patients with suspected cirrhosis or transition to cirrhosis must have an abdominal ultrasound, CT scan, or MRI scan without evidence of hepatocellular carcinoma and a serum AFP < 100 ng/mL within 2 months of randomization

• Negative urine or blood pregnancy test (for women of childbearing potential) documented within the 24-hour period prior to the first dose of study drug

• All fertile males and females receiving ribavirin must be using effective contraception during treatment and during the 6 months after treatment end

• Having a liver biopsy obtained within 5 years of this study is encouraged, but optional in accordance with local treatment traditions.

Exclusion Criteria:

• Women with ongoing pregnancy or breast feeding

• Previous non-response during treatment (as defined as having detectable HCV RNA = 50 IU/ml at the end of previous treatment) with pegylated interferon alfa-2a or alfa-2b combination therapy with ribavirin for at least 12 weeks and at most 24 weeks

• Less than 24 weeks have elapsed since the last dose of pegylated interferon or ribavirin in the previous treatment period prior to inclusion in this study.

• Therapy with any systemic anti-viral

• anti-neoplastic

• immunomodulatory treatment (including supraphysiologic doses of steroids and radiation) = 6 months prior to the first dose of study drug

• Any investigational drug = 6 weeks prior to the first dose of study drug. HCV genotype 1, 4, 5 or 6 infection

• Positive test at screening for anti-HAV IgM Ab

• HBsAg

• anti-HBc IgM Ab

• anti-HIV Ab

• Evidence of a medical condition associated with chronic liver disease other than HCV (e.g., hemochromatosis, autoimmune hepatitis, metabolic liver disease, alcoholic liver disease, toxin exposures)

• History or other evidence of decompensated liver disease

• Neutrophil count < 1500 cells/mm3 or platelet count < 75,000 cells/mm3 at screening

• Serum creatinine level > 2 mg/dl (> 124 µmol/L) or creatinine clearance < 50 ml/minute at screening

• Severe psychiatric disease, especially depression, as judged by the treating physician

• History of a severe seizure disorder or current anticonvulsant use

• History of immunologically mediated disease

• severe chronic pulmonary disease associated with functional limitation

• severe cardiac disease

• major organ transplantation or other evidence of severe illness

• malignancy

• any other conditions which would make the patient, in the opinion of the investigator, unsuitable for the study

• Thyroid dysfunction not adequately controlled (TSH and T4 levels out of normal range)

• Evidence of severe retinopathy (e.g. CMV retinitis, macula degeneration) or

• clinically relevant ophthalmological disorder due to diabetes mellitus or

• hypertension

• Evidence of drug abuse (including excessive alcohol consumption) in accordance with local therapeutic traditions. (Patients receiving Methadone or Subutex therapy may be included in this study.)

• Inability or unwillingness to provide informed consent or abide by the requirements of the study

• Male partners of women who are pregnant

• Hemoglobin < 11.3 g/dL (< 7.0 mmol/L) in women or < 12.9 g/dL (< 8.0 mmol/L) in men at screening.

• Any patient with an increased baseline risk for anemia (e.g. thalassemia, spherocytosis, etc) or for whom anemia would be medically problematic

• Patients with documented or presumed coronary artery disease or cerebrovascular disease should not be enrolled if, in the judgment of the investigator, an acute decrease in hemoglobin by up to 4 g/dL (as may be seen with ribavirin therapy) would not be well-tolerated

Study Design

Allocation: Non-Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Chronic Hepatitis C
• Hepatitis
• Hepatitis A
• Hepatitis C
• Hepatitis C, Chronic
• Hepatitis, Chronic

Intervention

Drug:
• Pegylated interferon alfa-2a and ribavirin
Arm A: Pegylated interferon alfa-2a Injection, 180 µg sc x 1/w for 48 weeks Ribavirin Tablet 200 mg weight based 5 or 6 per day for 48 weeks
• Pegylated interferon alfa-2a and ribavirin
Arm B:Pegylated interferon alfa-2a Injection, 180 µg sc x 1/w for 48 weeks Ribavirin Tablet 200 mg weight based 5 or 6 per day for 48 weeks
• Pegylated interferon alfa-2a and ribavirin
Arm C:Pegylated interferon alfa-2a Injection, 180 µg sc x 1/w for 24 weeks Ribavirin Tablet 200 mg weight based 5 or 6 per day for 24 weeks

Locations

Country	Name	City	State
Sweden	Dept of Infectious Diseases, Sahlgrenska University Hospital	Goteborg

Sponsors (2)

Lead Sponsor	Collaborator
Göteborg University	Hoffmann-La Roche

Country where clinical trial is conducted

Sweden, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Sustained viral response (SVR) rate defined as percentage of patients with non-detectable HCV-RNA 24 weeks after completion of the 24 or 48 week treatment period.		24 weeks after completion of the 24 or 48 week treatment period.	No
Secondary	Sustained viral response (SVR)rate and percentage of patients with normal serum ALT levels and its association with prespecified factors e.g. viral load		24 weeks after complection of the 24 or 48 week treatment	Yes