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Interferon-gamma With Interferon Alpha and Ribavirin for Hepatitis C Non-responders

Interferon-gamma With Interferon Alpha and Ribavirin for Hepatitis C Patients Who Are Non-responders to Interferon Alpha Plus Ribavirin

Status
Completed
Phases
Phase 2Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00538811
Enrollment
40
Registered
2007-10-03
Start date
Unknown
Completion date
Unknown
Last updated
2010-10-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Genotype 3, Hepatitis C, Non-responders, Relapsers

Brief summary

When administered simultaneously, interferon-alpha 2b + interferon-gamma result in dramatic antiviral synergy.Ribavirin has shown to enhance interferon-gamma levels in patients with chronic hepatitis C treated with interferon-alpha. Enhancement of immune responses, especially those related to type-1 T helper cell activity, may contribute to better efficacy in combining ribavirin with IFN-alpha for treatment of chronic hepatitis C. The aim of the present study is to evaluate the efficacy and safety of a triple regimen, a combination treatment with Interferon gamma, Interferon alfa-2b plus Ribavirin in patients who have not previously responded to interferon alpha in combination of ribavirin.

Interventions

DRUGinterferon alpha-2b, ribavirin, interferon-gamma,
DRUGinterferon alpha-2b, ribavirin, amantadine

Sponsors

Aga Khan University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* Non-responders and relapsers to previous interferon and ribavirin therapy given for six months * HCV genotype 3 * Compensated liver disease * Hb ≥10 g/dl (females),≥11 g/dl (males) * Platelets count ≥ 100,000 / cubic mm * Neutrophils count ≥1,500/cubic mm * ≥18 years to ≤ 70 years. * At least one abnormal ALT value in the last year. * TSH level within normal limits. * Non pregnant adult females. * Absence of drug or alcohol abuse. * Informed consent given by the patient

Exclusion criteria

* Patient younger than 18 yrs and older than 70 yrs. * Hepatitis B or HIV co-infection. * Severe renal dysfunction or creatinine clearance less than 50 ml/min * Pregnant women or breast feeding women. * Suspected hypersensitivity to Interferon alpha, gamma or ribavirin. * Decompensated liver cirrhosis. * History or any other evidence of other causes of CLD other than hepatitis C infection ( like hemochromatosis,, autoimmune hepatitis, metabolic liver disease, alcoholic liver disease, toxin exposure, Wilson's disease,Drug induced liver disease) * Active malignant disease. * Any known pre-existing medical condition that could interfere with subject's participation or completion of study such as psychiatric condition, seizures disorder requiring medications, co existing heart diseases, lung diseases, poorly controlled diabetes, auto immune diseases, gout) * History of interferon and/or ribavirin intolerance

Countries

Pakistan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026