Drug intelligence / Profile preview

valopicitabine + peginterferon alfa-2b

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

Overview

A combination investigational therapy for chronic hepatitis C virus (HCV) infection, specifically genotype 1, composed of valopicitabine (NM283), an oral small molecule prodrug of 2'-C-methylcytidine that inhibits HCV RNA polymerase (NS5B), and peginterferon alfa-2b, a recombinant, pegylated interferon that stimulates the innate antiviral immune response via activation of the type 1 interferon receptor and subsequent JAK/STAT signaling. The combination was developed as an alternative for patients not responding to standard therapies, aiming to improve sustained virological response rates in both treatment-naive and treatment-experienced populations. Clinical trials showed marked reductions in viral load and a notable percentage of patients achieving undetectable HCV RNA, though some trials suggested efficacy was not superior to standard of care and ribavirin was absent in combination arms[1][3][5].

Brand names
PEG-Intron
Other names
valopicitabine + pegylated interferonNM283 + peginterferon alfa-2b
02

Targets

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

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