Cipriano Alessandra, Kapil Ram P, Zhou Mingyan, Shet Manjunath S, Harris Stephen C, Apseloff Glen, Whiteside Garth T
Imbrium Therapeutics, Stamford, CT, United States.
Ohio Clinical Trials, Inc., Columbus, OH, United States.
Front Pharmacol. 2024 Aug 19;15:1432902. doi: 10.3389/fphar.2024.1432902. eCollection 2024.
Sunobinop is a novel, potent, selective partial agonist at nociceptin/orphanin FQ peptide (NOP) receptors. The primary objective of this randomized, double-blind, placebo-controlled study was to assess the next-day residual effects of an evening dose of sunobinop in healthy participants. Participants were randomized into 1 of 5 treatment sequences. Treatment consisted of 1 dose each of sunobinop 0.2, 0.6, 2, and 6 mg suspension and placebo suspension. Key pharmacodynamic (PD) measures included the digit symbol substitution test (DSST), Karolinska sleepiness scale (KSS), and body sway. The randomized safety population consisted of 25 participants. The DSST, KSS, and body sway showed dose-dependent effects following the administration of sunobinop, with no significant differences versus placebo at sunobinop doses <2 mg. At sunobinop 2 mg, PD effects were relatively small in magnitude and inconsistent. The last timepoint where significant differences between sunobinop 2 mg and placebo on the DSST, KSS, and body sway were observed was at 12 h, 16.5 h, and 13.5 h postdose, respectively. Sunobinop 6 mg resulted in larger and consistent PD effects, with significant differences from placebo at all timepoints up to 16.5-18 h postdose. Somnolence was the most frequently reported adverse event (AE), and all AEs were mild-to-moderate. No deaths occurred during the study or discontinuations due to an AE. Overall, a nighttime oral dose of sunobinop up to 2 mg was safe and generally well tolerated in healthy participants with limited next-day residual effects that were consistent with other sedative/hypnotic drugs.
苏诺比诺是一种新型、强效、选择性的孤啡肽/孤啡肽FQ肽(NOP)受体部分激动剂。这项随机、双盲、安慰剂对照研究的主要目的是评估健康参与者晚间服用苏诺比诺后的次日残留效应。参与者被随机分为5种治疗顺序中的1种。治疗包括分别服用0.2、0.6、2和6毫克苏诺比诺悬浮液及安慰剂悬浮液各1剂。关键药效学(PD)指标包括数字符号替换测验(DSST)、卡罗林斯卡嗜睡量表(KSS)和身体摇摆。随机安全人群包括25名参与者。服用苏诺比诺后,DSST、KSS和身体摇摆显示出剂量依赖性效应,苏诺比诺剂量<2毫克时与安慰剂无显著差异。苏诺比诺2毫克时,PD效应相对较小且不一致。在DSST、KSS和身体摇摆方面,观察到苏诺比诺2毫克与安慰剂有显著差异的最后时间点分别为给药后12小时、16.5小时和13.5小时。苏诺比诺6毫克产生了更大且一致的PD效应,给药后至16.5 - 18小时的所有时间点与安慰剂均有显著差异。嗜睡是最常报告的不良事件(AE),所有AE均为轻度至中度。研究期间未发生死亡,也没有因AE而停药的情况。总体而言,健康参与者夜间口服高达2毫克的苏诺比诺是安全的,且一般耐受性良好,次日残留效应有限,这与其他镇静/催眠药物一致。