Pharmacokinetics and metabolism of idebenone in healthy male subjects

Bodmer, Michael ; Vankan, Pierre ; Dreier, Manfred ; Kutz, Klaus ; Drewe, Jürgen

In: European Journal of Clinical Pharmacology, 2009, vol. 65, no. 5, p. 493-501

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    Summary
    Purpose: Idebenone is a synthetic analogue of ubiquinone that may be beneficial in the treatment of Friedreich's ataxia. Since in previous pharmacokinetic trials only lower doses were studied, it was the aim of this study to evaluate the pharmacokinetics of idebenone in higher doses of up to 2,250mg/day. Methods: In this open, randomized trial, 25 healthy male subjects received first either a single oral dose of 150mg or 750mg of idebenone, then the same dose given at 8-h intervals for 14days. Results: Idebenone and its metabolites appeared in the plasma quickly. Over 99% of parent idebenone was metabolized, indicating a high first-pass effect. Cmax and AUC0−t values for parent idebenone and its metabolites increased in a dose-proportional manner. There was virtually no accumulation of parent drug or metabolites following multiple dosing. Conclusions: Idebenone exhibited dose-dependent pharmacokinetics in daily doses up to 2,250mg. In 6/14 subjects, adverse events of mild to moderate severity were observed