Voxilaprevir + Voriconazole = Unknown or no reaction

Effect on Concentration

Voxilaprevir
Increase
Applies within class?
No
Voriconazole
Unknown
Applies within class?
No

Pharmacologic Effects

Effect
N/A
Applies within class?
No
Effect
N/A
Applies within class?
No

Interaction History

N/A

Last Updated 22-Nov-2022

Summary

The authors concluded that potent inhibition of CYP 3A resulted in a modest increase in GS-9857 concentrations, but that co-administration of GS-9857 with potent inhibitors of CYP 3A, including voriconazole, can be undertaken without dose modification.

Sources

Study Design

This was an open label, single and multiple dose four cohort study in 98 healthy volunteers. Participants were administered a single dose of GS-9857 100 mg alone or in combination with inhibitors or inducers of drug transporters or CYP isoenzymes. These drugs included rifampin 600 mg x 1 dose fasted, or rifampin 600 mg daily for seven days fed. Geometric means ratios and 90% Confidence Intervals for GS-9857 were estimated and compared to pre-specified lack of PK alteration boundaries 70% - 143%. Safety was assessed by routine laboratory and clinical monitoring. Five subjects discontinued the study drug during the study period.

Study Results

GS-9857 concentrations were modestly increased by multiple doses of voriconazole (AUC 1.8 fold, Cmax unchanged).

Study Conclusions

References

Kirby BJ, J Taylor, Stamm LM, Q Song, Y Li, A Mathias. Evaluation of pan genotypic hcv ns3/4a protease inhibitor gs-9857 as the object of transporter and cytochrome p450 mediated drug-drug interactions. 17th International Workshop On Clinical Pharmacology Of Hiv And Hepatitis Therapy. Washington, DC, USA. ; 2016.