Literature DB >> 27872071

Results of a Doravirine-Atorvastatin Drug-Drug Interaction Study.

Sauzanne Khalilieh1, Ka Lai Yee2, Rosa I Sanchez2, Ilias Triantafyllou2, Li Fan2, Noha Maklad2, Heather Jordan3, Maureen Martell4, Marian Iwamoto2.   

Abstract

Doravirine is a novel, highly potent, nonnucleoside reverse transcriptase inhibitor that is administered once daily and that is in development for the treatment of HIV-1 infection. In vitro and clinical data suggest that doravirine is unlikely to cause significant drug-drug interactions via major drug-metabolizing enzymes or transporters. As a common HIV-1 infection comorbidity, hypercholesterolemia is often treated with statins, including the commonly prescribed atorvastatin. Atorvastatin is subject to drug-drug interactions with cytochrome P450 3A4 (CYP3A4) inhibitors. Increased exposure due to CYP3A4 inhibition may lead to serious adverse events (AEs), including rhabdomyolysis. Furthermore, atorvastatin is a substrate for breast cancer resistance protein (BCRP), of which doravirine may be a weak inhibitor; this may increase atorvastatin exposure. The potential of doravirine to affect atorvastatin pharmacokinetics was investigated in a two-period, fixed-sequence study in healthy individuals. In period 1, a single dose of atorvastatin at 20 mg was administered followed by a 72-h washout. In period 2, doravirine at 100 mg was administered once daily for 8 days, with a single dose of atorvastatin at 20 mg concomitantly being administered on day 5. Sixteen subjects were enrolled, and 14 completed the trial; 2 discontinued due to AEs unrelated to the treatment. The atorvastatin area under the curve from time zero to infinity was similar with and without doravirine (geometric mean ratio [GMR] for doravirine-atorvastatin/atorvastatin, 0.98; 90% confidence interval [CI], 0.90 to 1.06), while the maximum concentration decreased by 33% (GMR for doravirine-atorvastatin/atorvastatin, 0.67; 90% CI, 0.52 to 0.85). These changes were deemed not to be clinically meaningful. Both of the study drugs were generally well tolerated. Doravirine had no clinically relevant effect on atorvastatin pharmacokinetics in healthy subjects, providing support for the coadministration of doravirine and atorvastatin.
Copyright © 2017 American Society for Microbiology.

Entities:  

Keywords:  CYP3A4; atorvastatin; doravirine; human immunodeficiency virus; hypercholesterolemia; pharmacokinetics

Mesh:

Substances:

Year:  2017        PMID: 27872071      PMCID: PMC5278756          DOI: 10.1128/AAC.01364-16

Source DB:  PubMed          Journal:  Antimicrob Agents Chemother        ISSN: 0066-4804            Impact factor:   5.191


  23 in total

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5.  The Effect of Single and Multiple Doses of Rifampin on the Pharmacokinetics of Doravirine in Healthy Subjects.

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6.  Doravirine and the Potential for CYP3A-Mediated Drug-Drug Interactions.

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7.  [Interaction between atorvastatin and voriconazole in rat plasma: a HPLC-MS/MS-based study].

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8.  Prediction of Cyclosporin-Mediated Drug Interaction Using Physiologically Based Pharmacokinetic Model Characterizing Interplay of Drug Transporters and Enzymes.

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Review 9.  Clinical Pharmacokinetics and Drug Interactions of Doravirine.

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