Key result
Administration of edoxaban 60 mg with a high-fat meal resulted in modest, clinically insignificant increases in pharmacokinetic parameters (6% to 22%) compared to the fasted state.
Why the study?
Does a standard high-fat meal affect the pharmacokinetics of a single 60 mg dose of edoxaban in healthy male volunteers?
RCT (n=32)
Open-label
Crossover
Does a standard high-fat meal affect the pharmacokinetics of a single 60 mg dose of edoxaban in healthy male volunteers?
Edoxaban can be administered without regard to food, as a high-fat meal produces only modest, clinically insignificant increases in its pharmacokinetic parameters.
Answers are grounded in this paper and cite their sources.
Edoxaban may be taken without regard to meals; confirms food-independent pharmacokinetics in this RCT.
The primary objective of this study was to assess the effect of a standard high-fat meal on the single-dose (60 mg) pharmacokinetics (PK) of edoxaban in healthy Japanese and Caucasian male volunteers matched by body mass index. This was an open-label, randomized, 2-period crossover study. All 32 enrolled volunteers completed the study per protocol. Both serial blood and urine samples were collected, and edoxaban concentrations were analyzed by a validated liquid chromatography/tandem mass spectrometry method. Activated partial thromboplastin and prothrombin times were obtained as measures of pharmacodynamic effect. The point estimates of the geometric mean ratios (fed/fasted) for AUC(0-t), AUC(0-∞), and C(max) demonstrated modest increases ranging from 6% to 22% across PK parameters for both race cohorts. The disposition was similar in both Japanese and Caucasian matched volunteers with slightly higher AUC values (ranging from 7%-9%) in Caucasians. There were no serious adverse events during the study. All drug-related adverse events were mild and self-limited, and none were bleeding related. Both Japanese and Caucasian volunteers demonstrated a modest but clinically insignificant food effect. It was concluded that edoxaban can be administered without regard to food.
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Mendell et al. (2010) conducted an RCT in Healthy volunteers (n=32). Edoxaban (fed state) vs. Fasted state was evaluated on Pharmacokinetics (AUC(0-t), AUC(0-∞), and C(max)) (6% to 22% increase). Administration of edoxaban 60 mg with a high-fat meal resulted in modest, clinically insignificant increases in pharmacokinetic parameters (6% to 22%) compared to the fasted state.
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