Neuroscience CEDD Discovery Medicine, GlaxoSmithKline, Verona, Italy.
Sleep. 2012 Aug 1;35(8):1097-104. doi: 10.5665/sleep.1996.
To assess the acute effects of SB-649868 in male subjects with Primary Insomnia with regard to (1) objective and subjective sleep parameters, (2) safety and tolerability, (3) next-day residual effects.
Multicenter, randomized, double-blind, placebo-controlled crossover study using a complete set of Williams orthogonal Latin Squares
9 sleep centers in Germany
52 male subjects with a diagnosis of primary insomnia (difficulty in sleep initiation and maintenance) confirmed by polysomnography
SB-649868 (10, 30, 60 mg) and placebo administered after dinner 90 minutes before bedtime
Sleep effects assessed by polysomnography during 2 consecutive nights and by sleep questionnaires completed by subjects after each night at the sleep laboratory. Safety and tolerability were assessed by adverse events collection, electrocardiogram (ECG), vital signs, laboratory tests. Next-day residual effects were assessed by Digit Symbol Substitution Test, and modified Verbal Learning Memory Test administered at "lights on" after night 2. SB-649868 significantly reduced latency to persistent sleep, wake after sleep onset (WASO), and increased total sleep time (TST) compared to placebo. A dose-dependent effect was observed. A dose-dependent increase in absolute and percent REM sleep and reduction in REM sleep latency was observed mainly at the 60-mg dose. SB-649868 was well tolerated with inconsistent next day residual effects. SB-649868 sleep effects were correlated with SB-649868 circulating levels.
The data demonstrate the sleep-promoting properties of the orexin antagonist SB-649868 in male patients with insomnia.
评估 SB-649868 在原发性失眠男性患者中的急性影响,具体涉及(1)客观和主观睡眠参数、(2)安全性和耐受性、(3)次日残留效应。
采用完整的威廉姆斯正交拉丁方,进行多中心、随机、双盲、安慰剂对照交叉研究。
德国 9 个睡眠中心
52 名男性原发性失眠患者(入睡和维持睡眠困难),经多导睡眠图(PSG)确诊
SB-649868(10、30、60mg)和安慰剂,于睡前 90 分钟晚餐后给药
通过连续 2 晚的多导睡眠图评估睡眠效果,并通过每位受试者在睡眠实验室后每夜填写的睡眠问卷进行评估。通过不良事件收集、心电图(ECG)、生命体征、实验室检查评估安全性和耐受性。次日残留效应通过数字符号替换测试和改良词语学习记忆测试进行评估,在第 2 夜“开灯”后进行。与安慰剂相比,SB-649868 显著缩短了入睡潜伏期、睡眠起始后觉醒(WASO)时间,并增加了总睡眠时间(TST)。观察到剂量依赖性效应。主要在 60mg 剂量下观察到 REM 睡眠时间的绝对和百分比增加以及 REM 睡眠潜伏期缩短。SB-649868 耐受性良好,次日残留效应不一致。SB-649868 的睡眠效应与 SB-649868 的循环水平相关。
数据表明,食欲素拮抗剂 SB-649868 具有促进睡眠的特性,可改善男性失眠患者的睡眠。