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Randomized Controlled Trial
. 2023 Nov;16(11):2276-2288.
doi: 10.1111/cts.13627. Epub 2023 Sep 25.

Pharmacokinetics, safety, and tolerability of inhaled remdesivir in healthy participants

Affiliations
Randomized Controlled Trial

Pharmacokinetics, safety, and tolerability of inhaled remdesivir in healthy participants

Rita Humeniuk et al. Clin Transl Sci. 2023 Nov.

Abstract

Intravenous remdesivir (RDV) is US Food and Drug Administration-approved for hospitalized and nonhospitalized individuals with coronavirus disease 2019. RDV undergoes intracellular metabolic activation to form the active triphosphate, GS-443902, and other metabolites. Alternative administration routes, including localized pulmonary delivery, can lower systemic exposure and maximize exposure at the site of action. This study evaluated the pharmacokinetics (PK) and safety of inhaled RDV in healthy adults. This phase Ia, randomized, placebo-controlled study evaluated inhaled RDV in healthy participants randomized 4:1 to receive RDV or placebo as single doses (4 cohorts) or multiple once-daily doses (3 cohorts). Doses in cohorts 1-6 were administered as an aerosolized solution for inhalation through a sealed facemask; doses in cohort 7 were administered as an aerosolized solution for inhalation through a mouthpiece. Safety was assessed throughout the study. Seventy-two participants were enrolled (inhaled RDV, n = 58 and placebo, n = 14). Following single RDV doses, RDV, GS-704277, and GS-441524 plasma PK parameters indicated dose-proportional increases in area under the concentration-time curve (AUC) extrapolated to infinite time, AUC from time zero to last quantifiable concentration, and maximum observed concentration. Analyte plasma concentrations after multiple RDV doses were consistent with those for single-dose RDV. Analyte plasma exposures were lower when RDV was administered with a mouthpiece versus a sealed facemask. The most common adverse events included nausea, dizziness, and cough. Single- and multiple-dose inhaled RDV exhibited linear and dose-proportional plasma PK. Administration of RDV via inhalation was generally safe and well-tolerated.

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Conflict of interest statement

R.H., S.C., S.E., O.A., D.X., A.S., S.D., J.L., A.O., H.W., S.G., R.P., and M.D. are employees and stockholders of Gilead Sciences, Inc. K.J. is a former employee and stockholder of Gilead Sciences, Inc. and a current employee of Corcept Therapeutics. M.J. is an employee of ICON plc. A.dZ. is a former employee and stockholder of Gilead Sciences, Inc. and a current employee of Atea Pharmaceuticals.

Figures

FIGURE 1
FIGURE 1
Mean (SD) plasma concentration versus time for (a) RDV, (b) GS‐704277, and (c) GS‐441524 for single‐dose RDV and (d) RDV, (e) GS‐704277, and (f) GS‐441524 for multiple‐dose RDV administered via inhalation. FM, facemask; LLOQ, lower limit of quantification; MP, mouthpiece; RDV, remdesivir. Error bars denote standard deviations. aTime from start of nebulization.

References

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