Department of Clinical Pharmacology, Idorsia Pharmaceuticals Ltd, Allschwil, Switzerland.
Parexel International GmbH, Berlin, Germany.
Eur Neuropsychopharmacol. 2021 Oct;51:90-104. doi: 10.1016/j.euroneuro.2021.05.005. Epub 2021 Jun 5.
Daridorexant (ACT-541468) is a new dual orexin receptor antagonist being evaluated for the treatment of insomnia, which is a common comorbidity of depression and anxiety. Therefore, daridorexant is likely to be administered concomitantly with agents (e.g., citalopram) used to treat these disorders. In this single-centre, single-blind, randomized, placebo-controlled, sequential design Phase 1 study with the inclusion of two double-blind crossover parts, the pharmacokinetic (PK; blood sampling at regular intervals) and pharmacodynamic (PD; battery of objective and subjective PD tests performed at regular intervals) interactions between daridorexant (50 mg) and citalopram (20 mg, single dose and at steady state) as well as the safety/tolerability in healthy subjects were investigated. There were no relevant effects of citalopram (single dose/steady state) on daridorexant exposure and vice versa. PD variables measured after morning administration of daridorexant alone showed effects consistent with a sleep-promoting compound. Only co-administration of daridorexant with citalopram at steady state led to relevant changes in objective (unstable tracking) and subjective (visual analogue scale alertness and Karolinska Sleepiness Scale) PD endpoints compared to daridorexant alone. No serious or severe adverse events were reported, while no clinically relevant treatment-emergent effects on ECG parameters, clinical laboratory, or vital signs were observed. In conclusion, the co-administration of daridorexant and citalopram lead to only minor changes in PK parameters, while performance of PD assessments following co-administration were mainly driven by the expected central nervous system effects of daridorexant. Doses up to 50 mg daridorexant can be safely co-administered with citalopram.
达理多雷克斯ant(ACT-541468)是一种新的双重食欲素受体拮抗剂,正在评估用于治疗失眠,失眠是抑郁和焦虑的常见合并症。因此,达理多雷克斯ant 可能与用于治疗这些疾病的药物(例如西酞普兰)同时给药。在这项包括两个双盲交叉部分的单中心、单盲、随机、安慰剂对照、序贯设计的 1 期研究中,研究了达理多雷克斯ant(50mg)和西酞普兰(20mg,单次剂量和稳态)之间的药代动力学(PK;定期采血)和药效学(PD;定期进行一系列客观和主观 PD 测试)相互作用以及健康受试者的安全性/耐受性。西酞普兰(单次剂量/稳态)对达理多雷克斯ant 暴露没有相关影响,反之亦然。单独给予达理多雷克斯ant 后早晨测量的 PD 变量显示出与促进睡眠化合物一致的作用。只有达理多雷克斯ant 与西酞普兰在稳态时联合给药,与单独给予达理多雷克斯ant 相比,才会导致客观(不稳定跟踪)和主观(视觉模拟量表警觉性和 Karolinska 睡眠量表)PD 终点的相关变化。未报告严重或严重不良事件,也未观察到心电图参数、临床实验室或生命体征的临床相关治疗后出现的影响。总之,达理多雷克斯ant 和西酞普兰联合给药仅导致 PK 参数的微小变化,而联合给药后进行 PD 评估主要是由达理多雷克斯ant 的预期中枢神经系统作用驱动的。高达 50mg 的达理多雷克斯ant 可以与西酞普兰安全联合给药。