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ribavirin + interferon alpha-2a
- Development stage
- Unknown
- Lead developer
- Roche
- Modality
- Orthosteric Ligands → Classical Binding Small Molecules → Small Molecules, DNA Intercalators/Alkylators → Nucleic Acid-Directed Small Molecules → Small Molecules, Metabolically Activated Prodrugs → Prodrugs/Conditional Activator Small Molecules → Small Molecules, Cytokines & Interferons → Recombinant Proteins and Enzymes
- Administration
- Oral, Subcutaneous
01
Overview
This drug is a combination therapy consisting of ribavirin, a synthetic guanosine nucleoside antiviral agent, and interferon alpha-2a (often in its pegylated form as peginterferon alfa-2a), a recombinant cytokine. The combination is primarily used for the treatment of chronic hepatitis C virus (HCV) infection. Ribavirin inhibits viral RNA synthesis and mRNA capping by acting as a nucleoside analog after intracellular phosphorylation. Interferon alpha-2a binds to type 1 interferon receptors on host cells, activating the JAK/STAT pathway and inducing an innate antiviral response through upregulation of multiple genes involved in immune defense. This dual mechanism targets both viral replication directly (ribavirin) and enhances host immune response against HCV (interferon). The combination was considered first-line therapy before the advent of direct acting antivirals but remains notable for its broad-spectrum antiviral activity[1][4][5][6].
- Other names
- ribavirin and interferon alpha-2aribavirin plus interferon alpha-2aribavirin + peginterferon alfa-2a
02
Targets
RdRp (Coronavirus RNA-dependent RNA polymerase)IFNAR2 (Interferon alpha/beta receptor subunit 2)IFNAR (Immune system modulation via type I interferon receptor)vCE (Viral mRNA capping enzyme)IMPDH (Inosine-5'-monophosphate dehydrogenase 1)
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