Drug intelligence / Profile preview

sofosbuvir + velpatasvir + voxilaprevir + ribavirin

Development stage
Phase 4
Lead developer
Gilead Sciences
Modality
Small Molecules
Administration
Oral
01

Overview

A four-drug combination regimen consisting of **sofosbuvir**, **velpatasvir**, **voxilaprevir**, and **ribavirin**, developed together for the treatment of chronic hepatitis C virus (HCV) infection, especially in patients who have previously failed direct-acting antiviral therapies. - Sofosbuvir is a nucleotide analog HCV NS5B polymerase inhibitor, blocking viral RNA synthesis. - Velpatasvir inhibits HCV NS5A, a viral protein that impacts RNA replication and assembly. - Voxilaprevir is an HCV NS3/4A protease inhibitor, preventing viral polyprotein processing. - Ribavirin is a nucleoside analog with broad-spectrum antiviral activity; its precise mechanism in HCV is not fully defined but is thought to involve inhibition of viral RNA synthesis and immune modulation. This combination has been studied for salvage therapy in patients with chronic HCV infection, including those with and without cirrhosis[3].

02

Targets

NS3/4A (Hepatitis C virus nonstructural protein 3/4A serine protease)NS5A (Hepatitis C virus nonstructural protein 5A (genotype 1b))NS5B (Hepatitis C virus non-structural protein 5B (NS5B) RNA-dependent RNA polymerase)IMPDH (Inosine-5'-monophosphate dehydrogenase 1)

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