Drug intelligence / Profile preview

INX-08189 + peginterferon alfa-2a + ribavirin

Development stage
Unknown
Lead developer
Bristol Myers Squibb
Modality
Recombinant Proteins and Enzymes, Small Molecules
Administration
Oral, Subcutaneous
01

Overview

INX-08189 + peginterferon alfa-2a + ribavirin is a triple combination therapy developed for the treatment of **chronic hepatitis C virus (HCV) infection**.\ - **INX-08189** is an orally administered phosphoramidate prodrug of 6-O-methyl-2'-C-methyl guanosine, acting as a potent inhibitor of HCV replication by targeting the viral RNA-dependent RNA polymerase NS5b, thereby blocking viral RNA synthesis[1][3][5].\ - **Peginterferon alfa-2a** is a pegylated recombinant interferon that induces antiviral, immunomodulatory, and antiproliferative effects through the stimulation of the host's immune response and upregulation of interferon-stimulated genes[2][4].\ - **Ribavirin** is a nucleoside analogue that interferes with viral RNA synthesis, leading to lethal mutagenesis and inhibition of viral replication[2][4].\ The combination shows synergy and increased efficacy compared to dual therapy in HCV, especially genotype 1b, with notable improvements in sustained virological response rates and a favorable safety profile[1][2][3][4][6].

Other names
6-O-methyl-2'-C-methyl guanosine phosphoramidate prodrugpegylated interferon alfa-2aribavirin
02

Targets

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

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