Idorsia Pharmaceuticals Ltd, Clinical Pharmacology, Allschwil Switzerland.
Idorsia Pharmaceuticals Ltd, Clinical Science, Allschwil, Switzerland.
Biomed Pharmacother. 2021 Jan;133:110955. doi: 10.1016/j.biopha.2020.110955. Epub 2020 Nov 12.
BACKGROUND/AIMS: The aim of this single-center, double-blind study was to investigate the effect of a 4-week once daily administration of 200 mg almorexant on tear film break-up time, spermatogenesis, hormone levels, and pancreatic elastase in stool in healthy male subjects.
Almorexant 200 mg or matching placebo was administered in the evening for 4 weeks once daily to 56 healthy male subjects. Changes in ophthalmological variables, sperm composition, hormone levels, and pancreatic elastase levels in stool were evaluated periodically up to 8 weeks after discontinuation of drug administration. Blood samples for pharmacokinetic measurements were taken after 4 weeks to confirm compliance to study drug intake.
The results of this study revealed no treatment effects of almorexant, neither on tear film break-up time nor on other ophthalmological variables investigated during this study. Furthermore, spermatogenesis, hormones of the hypothalamic-pituitary-adrenal and -gonadal axes, and endocrine pancreatic secretion were shown to be not affected by a 4-week once daily administration of almorexant.
Almorexant was well tolerated and had no effect on the spectrum of pharmacodynamic variables assessed. Ophthalmology and testicular findings detected in preclinical studies were not observed in this clinical study. Therefore, these preclinical findings appear not to be relevant for humans and do not prevent from conducting larger clinical trials with either healthy subjects or patients.
背景/目的:本单中心、双盲研究的目的是探讨 4 周每日一次给予 200mg 阿莫雷克斯坦对健康男性受试者泪膜破裂时间、精子发生、激素水平和粪便中胰腺弹性蛋白酶的影响。
56 名健康男性受试者每晚睡前接受 200mg 阿莫雷克斯坦或匹配安慰剂治疗,每日一次,持续 4 周。停药后 8 周内定期评估眼科变量、精子成分、激素水平和粪便中胰腺弹性蛋白酶水平的变化。在第 4 周后采集血样进行药代动力学测量,以确认研究药物摄入的依从性。
这项研究的结果表明,阿莫雷克斯坦既没有影响泪膜破裂时间,也没有影响本研究中其他眼科变量。此外,精子发生、下丘脑-垂体-性腺和性腺轴的激素以及内分泌胰腺分泌均不受 4 周每日一次给予阿莫雷克斯坦的影响。
阿莫雷克斯坦耐受性良好,对评估的药效学变量谱没有影响。在临床前研究中检测到的眼科和睾丸发现未在本临床研究中观察到。因此,这些临床前发现似乎与人类无关,不会妨碍对健康受试者或患者进行更大规模的临床试验。