Drug intelligence / Profile preview

samatasvir + omeprazole

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

Overview

Samatasvir + omeprazole is an investigational drug combination consisting of samatasvir, a hepatitis C virus (HCV) non-structural protein 5A (NS5A) inhibitor, and omeprazole, a proton pump inhibitor (PPI) commonly used to reduce gastric acid secretion. Samatasvir acts by inhibiting the replication of HCV through targeting the NS5A protein, a key regulator in the hepatitis C viral life cycle[2][6][10]. Omeprazole decreases stomach acid to manage gastrointestinal symptoms and, in this context, is generally studied for potential drug-drug interactions with samatasvir given its effect on gastric pH, which can impact the absorption of some antiviral agents[2][10]. Clinical studies have assessed the safety, pharmacokinetics, and possible interactions between these two drugs, particularly focusing on whether omeprazole affects the absorption or efficacy of samatasvir[2][10].

Brand names
PriLOSECPriLOSEC OTCFIRST OmeprazoleZegerid
02

Targets

ATP4A (Potassium–transporting ATPase alpha chain 1)NS5A (Hepatitis C virus nonstructural protein 5A (genotype 1b))

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