Drug intelligence / Profile preview

samatasvir + simeprevir + ribavirin

Development stage
Unknown
Lead developer
Merck
Modality
Small Molecules
Administration
Oral
01

Overview

A combination therapy of **samatasvir** (IDX719), **simeprevir** (TMC435), and **ribavirin** is an investigational, all-oral, direct-acting antiviral regimen studied for the treatment of chronic hepatitis C virus (HCV) infection. - **Samatasvir** is an NS5A inhibitor targeting HCV replication complex. - **Simeprevir** is an NS3/4A protease inhibitor that blocks viral protein processing, preventing HCV maturation[2][4][5]. - **Ribavirin** is a nucleoside analog with broad-spectrum antiviral activity, generally used in combination with other agents to enhance efficacy. This combination was evaluated in clinical trials (not approved for marketing) for safety, tolerability, efficacy, and pharmacokinetics in treatment-naïve adults with HCV genotypes 1b, 4, and 6, sometimes with additional antivirals. The regimen aimed to provide potent, interferon-free treatment for chronic HCV infection with the goal of achieving a sustained virologic response[3][6][8].

Other names
samatasvir + simeprevir + RBV
02

Targets

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

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