首页> 外文期刊>The journal of clinical psychiatry >Triple-bead mixed amphetamine salts (SPD465), a novel, enhanced extended-release amphetamine formulation for the treatment of adults with ADHD: a randomized, double-blind, multicenter, placebo-controlled study.
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Triple-bead mixed amphetamine salts (SPD465), a novel, enhanced extended-release amphetamine formulation for the treatment of adults with ADHD: a randomized, double-blind, multicenter, placebo-controlled study.

机译:三珠混合苯丙胺盐(SPD465),一种新型,增强型缓释苯丙胺制剂,用于治疗ADHD成人:一项随机,双盲,多中心,安慰剂对照研究。

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INTRODUCTION: The efficacy and safety of triple-bead mixed amphetamine salts (MAS), an oral, once-daily, enhanced extended-release amphetamine formulation designed for a duration of action up to 16 hours, were evaluated in adults with attention-deficit/hyperactivity disorder (ADHD). METHOD: In this phase 3, 7-week, randomized, double-blind, multicenter, placebo-controlled, parallel-group, dose-optimization study of 272 adults with ADHD (DSM-IV-TR criteria), subjects (aged 18 to 55 years) were randomly assigned to triple-bead MAS (starting dose 12.5 mg) or placebo. The primary outcome measure was change in ADHD Rating Scale-IV (ADHD-RS-IV). Secondary outcome measures included Clinical Global Impressions (CGI) scale, Time-Sensitive ADHD Symptom Scale (TASS) (measuring extended duration), Brown Attention-Deficit Disorder Scale (BADDS) (measuring executive function), Adult ADHD Impact Module (AIM-A) (measuring quality of life [QOL]), and ADHD-RS-IV hyperactivity-impulsivity and inattentiveness subscales. Adverse events (AEs), vital signs, electrocardiograms (ECGs), and laboratory data were collected. The trial was conducted from January 2005 to June 2005. RESULTS: Triple-bead MAS resulted in significantly greater improvement versus placebo in mean ADHD-RS-IV total score change (p < .0001), CGI-Improvement (p < .0001), TASS total score at 13-16 hours postdose (p = .002), BADDS total score (p < .0001), all AIM-A domains (p < or = .01), and ADHD-RS-IV subscales (p < .01), demonstrating extended duration of efficacy and improvements in executive function and QOL. The most common treatment-emergent AEs included insomnia, dry mouth, decreased appetite and weight, and headache. Most treatment-emergent AEs were mild or moderate in severity. CONCLUSIONS: Triple-bead MAS was significantly more effective than placebo in treating adult ADHD. The extended duration of action up to 16 hours and significant improvements in executive function and QOL address unique treatment needs of adults with ADHD. Treatment-emergent AEs with triple-bead MAS were consistent with amphetamine treatment.
机译:简介:对于成人注意力缺陷/成人,评估了三珠混合苯丙胺盐(MAS)的有效性和安全性,这是一种口服,每天一次的增强释放型苯丙胺制剂,设计作用时间长达16小时。多动症(ADHD)。方法:在这个为期3、7周的随机,双盲,多中心,安慰剂对照,平行组剂量优化研究中,该研究对272名ADHD(DSM-IV-TR标准)的成年人(18岁至55岁)随机分配给三珠MAS(起始剂量12.5 mg)或安慰剂。主要结果指标是ADHD评分量表IV(ADHD-RS-IV)的变化。次要结局指标包括临床总体印象(CGI)量表,时间敏感性ADHD症状量表(TASS)(测量持续时间),布朗注意缺陷障碍量表(BADDS)(测量执行功能),成人ADHD影响模块(AIM-A )(测量生活质量[QOL]),以及ADHD-RS-IV多动症-冲动和注意力不集中分量表。收集不良事件(AE),生命体征,心电图(ECG)和实验室数据。该试验于2005年1月至2005年6月进行。结果:与安慰剂相比,三珠MAS的平均ADHD-RS-IV总得分变化(p <.0001),CGI改善(p <.0001)的改善明显大于安慰剂。 ,给药后13-16小时的TASS总分(p = .002),BADDS总分(p <.0001),所有AIM-A域(p <或= .01)和ADHD-RS-IV子量表(p <.01),表明疗效持续时间延长,执行功能和QOL改善。最常见的治疗性不良事件包括失眠,口干,食欲和体重下降以及头痛。大多数出现治疗的AEs的严重程度为轻度或中度。结论:三珠MAS治疗成人多动症的疗效明显优于安慰剂。延长的动作时间长达16小时,执行功能和QOL的显着改善满足了ADHD成人的独特治疗需求。出现三珠MAS的治疗性不良事件与苯丙胺治疗一致。

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