Title : Drug-Drug Interactions with the NS3/4A Protease Inhibitor Simeprevir.

Pub. Date : 2016 Feb

PMID : 26353895






3 Functional Relationships(s)
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1 Simeprevir is metabolized by the cytochrome P450 (CYP) system, primarily CYP3A, and is a substrate for several drug transporters, including the organic anion transporting polypeptides (OATPs). Simeprevir cytochrome P450 family 3 subfamily A member 4 Homo sapiens
2 It is susceptible to metabolic drug-drug interactions with drugs that are moderate or strong CYP3A inhibitors (e.g. ritonavir and erythromycin) or CYP3A inducers (e.g. rifampin and efavirenz); coadministration of these drugs may increase or decrease plasma concentrations of simeprevir, respectively, and should be avoided. Simeprevir cytochrome P450 family 3 subfamily A member 4 Homo sapiens
3 Clinical studies have shown that simeprevir is a mild inhibitor of CYP1A2 and intestinal CYP3A but does not inhibit hepatic CYP3A. Simeprevir cytochrome P450 family 3 subfamily A member 4 Homo sapiens