Drug intelligence / Profile preview

pegylated interferon alfa-2a + ribavirin

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

Overview

This combination therapy consists of pegylated interferon alfa-2a and ribavirin, which served as the standard of care for chronic hepatitis C virus (HCV) infection prior to the widespread adoption of all-oral direct-acting antiviral (DAA) regimens. Pegylated interferon alfa-2a is a conjugate of recombinant interferon alfa-2a with a 40 kDa branched polyethylene glycol chain, which enhances its pharmacokinetic profile by significantly extending its half-life. It works by binding to the interferon alpha/beta receptors, triggering a signaling cascade that induces an antiviral state in host cells. Ribavirin is a synthetic guanosine analog that exerts broad-spectrum antiviral effects through multiple mechanisms, including the inhibition of inosine-5'-monophosphate dehydrogenase (IMPDH), interference with viral RNA polymerase, and the induction of lethal mutagenesis in the viral genome. In the context of the PROGRESSIVE-C study conducted by Parc de Salut Mar, this regimen was evaluated for its efficacy and safety in patients with HCV-related cirrhosis, specifically focusing on its impact on portal hypertension and gastroesophageal varices.

Brand names
PegasysCopegusRebetolRibasphere
Other names
PEG-IFN + RBVPeginterferon alfa-2a plus ribavirinPegylated interferon alfa-2a and ribavirin
02

Targets

IFNAR (Immune system modulation via type I interferon receptor)IMPDH (Inosine-5'-monophosphate dehydrogenase 1)NS5B (Hepatitis C virus non-structural protein 5B (NS5B) RNA-dependent RNA polymerase)IFNAR2 (Interferon alpha/beta receptor subunit 2)

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