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Safety, pharmacokinetics, pharmacodynamics, and bioavailability of GSK2018682, a sphingosine‐1‐phosphate receptor modulator, in healthy volunteers
Author(s) -
Xu Jianfeng,
Gray Frank,
Henderson Alex,
Hicks Kirsty,
Yang Jiansong,
Thompson Paul,
Oliver Johann
Publication year - 2014
Publication title -
clinical pharmacology in drug development
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.711
H-Index - 22
eISSN - 2160-7648
pISSN - 2160-763X
DOI - 10.1002/cpdd.98
Subject(s) - pharmacokinetics , medicine , bradycardia , pharmacodynamics , tolerability , bioavailability , pharmacology , heart rate , crossover study , adverse effect , placebo , anesthesia , blood pressure , alternative medicine , pathology
Abstract The tolerability, pharmacokinetics, and pharmacodynamics of single (SD) and repeat (RD) doses of GSK2018682, a selective S1P1 receptor modulator, were evaluated in healthy volunteers. The bioavailability (BA) of different formulations and effects of food were also evaluated. SD of up to 24 mg and RD of up to 6 mg/day for 28 days were reasonably tolerated, despite higher incidences of gastrointestinal and cardiovascular adverse events compared to placebo. There was a linear relationship between dose and systemic exposure with a dose‐independent half‐life (t 1/2 ) between 44.9 and 63.3 hours. GSK2018682 induced acute, transient and non‐symptomatic decreases in heart rate and blood pressure. Dose‐dependent reduction in absolute lymphocyte count (ALC), and all tested subsets, was observed to various degrees, up to a nadir of over 70% reduction from baseline. There was no difference in major pharmacokinetic parameters among three formulations of GSK2018682 and between fasted and fed subjects. However, there was a reduction in the extent of bradycardia following dosing in the fed state. Additionally, exercise induced robust increase in heart rate in subjects who had bradycardia following RD of GSK2018682 up to 6 mg, suggesting possible physiological methods of reducing the extent of S1P mediated bradycardia and subsequent AV‐block.