Drug intelligence / Profile preview

paritaprevir + ritonavir + ombitasvir + dasabuvir + ribavirin

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

Overview

This drug is a fixed-dose combination of four direct acting antivirals—paritaprevir, ritonavir, ombitasvir, and dasabuvir—used with or without ribavirin for the treatment of chronic hepatitis C virus (HCV) infection, particularly genotype 1. Paritaprevir is an HCV NS3/4A protease inhibitor that blocks viral replication by inhibiting polyprotein cleavage. Ritonavir acts as a pharmacokinetic booster by inhibiting CYP3A-mediated metabolism to increase paritaprevir levels but has no direct anti-HCV activity. Ombitasvir is an HCV NS5A inhibitor that interferes with viral RNA replication and virion assembly. Dasabuvir is a non-nucleoside NS5B polymerase inhibitor that impedes HCV RNA-dependent RNA polymerase activity required for viral replication. Ribavirin is a nucleoside analog antiviral used in combination to enhance efficacy in certain patient populations[1][2][6][8]. The regimen was developed by AbbVie and marketed as Viekira Pak or Viekira Pak-RBV.

Brand names
Viekira Pak-RBV
Other names
PrOD regimen3D regimenparitaprevir/ritonavir/ombitasvir plus dasabuvir with ribavirin
02

Targets

NS5B (Hepatitis C virus non-structural protein 5B (NS5B) RNA-dependent RNA polymerase)NS5A (Hepatitis C virus nonstructural protein 5A (genotype 1b))CYP3A7 (Cytochrome P450 3A7)IMPDH (Inosine-5'-monophosphate dehydrogenase 1)NS3/4A (Hepatitis C virus nonstructural protein 3/4A serine protease)

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