Drug intelligence / Profile preview

peginterferon + ribavirin

Development stage
Unknown
Lead developer
Roche
Modality
Cytokines & Interferons → Recombinant Proteins and Enzymes, Small Molecules
Administration
Subcutaneous, Oral
01

Overview

A combination therapy comprising a pegylated interferon (either peginterferon alfa-2a or peginterferon alfa-2b) and the nucleoside analog ribavirin. This regimen was the standard of care for chronic hepatitis C virus (HCV) infection for over a decade prior to the introduction of direct-acting antivirals (DAAs). Peginterferon is a cytokine that binds to the Type I interferon receptor (IFNAR1/2), activating the JAK-STAT signaling pathway to induce an antiviral state in host cells and modulate the immune response. Ribavirin is a synthetic guanosine analog that exerts antiviral effects through multiple mechanisms, including inhibition of the viral RNA-dependent RNA polymerase (NS5B), inhibition of host inosine-5'-monophosphate dehydrogenase (IMPDH), and induction of lethal mutagenesis in the viral genome. The specific context of the Azienda Ospedaliera di Padova refers to a Phase 4 observational study evaluating the real-world efficacy, safety, and cost-effectiveness of these regimens in treatment-naive patients.

Other names
Peg-IFN + RBVpeginterferon alfa-2a + ribavirinpeginterferon alfa-2b + ribavirin
02

Targets

NS5B (Hepatitis C virus non-structural protein 5B (NS5B) RNA-dependent RNA polymerase)IFNAR (Immune system modulation via type I interferon receptor)IFNAR2 (Interferon alpha/beta receptor subunit 2)IMPDH (Inosine-5'-monophosphate dehydrogenase 1)nsp16 (Non-structural protein 16/Non-structural protein 10 complex)nsp14 (SARS-CoV-2 non-structural protein 14)IFNAR1 (Interferon alpha/beta receptor 1)

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