Agrawal N G, Porras A G, Matthews C Z, Woolf E J, Miller J L, Mukhopadhyay S, Neu D C, Gottesdiener K M
Department of Drug Metabolism, Merck Research Laboratories, West Point, Pennsylvania 19486, USA.
J Clin Pharmacol. 2001 Oct;41(10):1106-10. doi: 10.1177/00912700122012715.
To assess dose proportionality of etoricoxib across the anticipated clinical dose range, a single panel of 12 healthy subjects was administered single oral doses of etoricoxib of 5, 10, 20, 40, and 120 mg in an open, two-part, five-period crossover study. Plasma samples were collected aftereach dose and analyzed for etoricoxib concentrations. The pharmacokinetics of etoricoxib appear to be linear over the entire dose range examined, from 5 to 120 mg. Etoricoxib was found to be well tolerated across the 5 to 120 mg dose range.
为评估依托考昔在预期临床剂量范围内的剂量比例关系,在一项开放、两部分、五周期交叉研究中,对一组12名健康受试者单次口服5、10、20、40和120 mg依托考昔。每次给药后采集血浆样本并分析依托考昔浓度。在5至120 mg的整个检查剂量范围内,依托考昔的药代动力学似乎呈线性。发现在5至120 mg剂量范围内依托考昔耐受性良好。