Drug intelligence / Profile preview

VCH-916

Development stage
Phase 1
Lead developer
Vertex
Modality
Small Molecules
Administration
Oral
01

Overview

VCH-916 is a novel non-nucleoside inhibitor of the hepatitis C virus (HCV) NS5B RNA-dependent RNA polymerase. It acts as an allosteric inhibitor targeting the NS5B polymerase and has demonstrated sub-micromolar inhibitory activity against HCV replicons of genotypes 1a and 1b. The compound was developed for oral administration and exhibits high bioavailability with favorable absorption, distribution, metabolism, and excretion (ADME) properties. Preclinical studies showed extensive plasma protein binding (>98%) and low potential for drug-drug interactions via CYP inhibition or induction. Clinical development reached Phase 1 trials in patients with chronic hepatitis C infection to evaluate safety, tolerability, pharmacokinetics, and antiviral efficacy[1][2][4][7].

Other names
potassium 5-(cyclohex-1-en-1-yl)-3-(N-(4-methoxycyclohexyl)-4-methylcyclohexanecarboxamido)thiophene-2-carboxylate2-Thiophenecarboxylic acid, 5-(1-cyclohexen-1-yl)-3-[N-(4-methoxycyclohexyl)-4-methylcyclohexanecarboxamido]CAS Number 1200133-34-1
02

Targets

NS5B (Hepatitis C virus non-structural protein 5B (NS5B) RNA-dependent RNA polymerase)

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