Department of Psychiatry and NYU Langone Medical Center, New York, New York, USA.
Department of Child and Adolescent Psychiatry, NYU Langone Medical Center, New York, New York, USA.
J Child Adolesc Psychopharmacol. 2020 Sep;30(7):427-438. doi: 10.1089/cap.2020.0012. Epub 2020 May 19.
In two studies of adult attention-deficit/hyperactivity disorder (ADHD), SHP465 mixed amphetamine salts (MAS) extended-release significantly reduced ADHD-Rating Scale, 4th Edition total score (ADHD-RS-IV-TS) versus placebo (PBO). This report describes analyses of SHP465 MAS treatment response and remission rates from those studies. Adults with Diagnostic and Statistical Manual of Mental Disorders, 4th Edition, Text Revision-defined ADHD were randomized to SHP465 MAS (12.5-75 mg) or PBO in a 7-week dose-optimization study and to SHP465 MAS (25, 50, or 75 mg) or PBO in a 6-week fixed-dose study. Response was examined using three definitions (definition 1: ≥30% ADHD-RS-IV-TS reduction + Clinical Global Impressions-Improvement [CGI-I] rating of 1 or 2; definition 2: ≥50% ADHD-RS-IV-TS reduction + CGI-I rating of 1 or 2; definition 3: ADHD-RS-IV-TS ≤18). Remission was defined as ADHD-RS-IV-TS ≤12. The Kaplan-Meier analyses assessed time to response or remission. The intent-to-treat populations included 136 SHP465 MAS and 132 PBO participants in the dose-optimization study and 302 SHP465 MAS and 103 PBO participants in the fixed-dose study. Percentages of participants meeting response criteria (SHP465 MAS vs. PBO) at the final treatment week in the dose-optimization and fixed-dose studies, respectively, were 66.0% versus 31.6% and 72.7% versus 28.3% (definition 1); 47.9% versus 27.6% and 60.6% versus 16.7% (definition 2); and 54.3% versus 30.3% and 52.6% versus 18.3% (definition 3). The remission criterion (SHP465 MAS vs. PBO) at the final treatment week was met by 37.2% versus 19.7% of participants in the dose-optimization study and 39.7% versus 10.0% of participants in the fixed-dose study. Times to response and remission favored SHP465 MAS over PBO in both studies (all nominal log-rank < 0.0001). These analyses indicate that SHP465 MAS was associated with greater response and remission rates than PBO in adults with ADHD, with times to response and remission also nominally favoring SHP465 MAS.
在两项成人注意力缺陷/多动障碍(ADHD)的研究中,SHP465 混合安非他命盐(MAS)缓释剂与安慰剂(PBO)相比,显著降低了 ADHD 评定量表第四版总分(ADHD-RS-IV-TS)。本报告描述了来自这些研究的 SHP465 MAS 治疗反应和缓解率的分析。
符合精神障碍诊断与统计手册,第四版,文字修订版定义的 ADHD 的成年人被随机分配至 SHP465 MAS(12.5-75mg)或 PBO 进行为期 7 周的剂量优化研究,以及 SHP465 MAS(25、50 或 75mg)或 PBO 进行为期 6 周的固定剂量研究。使用三种定义来检查反应(定义 1:ADHD-RS-IV-TS 减少≥30%+临床总体印象改善[CGI-I]评分为 1 或 2;定义 2:ADHD-RS-IV-TS 减少≥50%+CGI-I 评分为 1 或 2;定义 3:ADHD-RS-IV-TS≤18)。缓解定义为 ADHD-RS-IV-TS≤12。Kaplan-Meier 分析评估了反应或缓解的时间。意向治疗人群包括剂量优化研究中的 136 名 SHP465 MAS 和 132 名 PBO 参与者,以及固定剂量研究中的 302 名 SHP465 MAS 和 103 名 PBO 参与者。在剂量优化和固定剂量研究的最后治疗周,分别达到反应标准(SHP465 MAS 与 PBO)的参与者比例为 66.0%比 31.6%和 72.7%比 28.3%(定义 1);47.9%比 27.6%和 60.6%比 16.7%(定义 2);以及 54.3%比 30.3%和 52.6%比 18.3%(定义 3)。在最后治疗周达到缓解标准(SHP465 MAS 与 PBO)的参与者比例分别为剂量优化研究中的 37.2%和 19.7%,固定剂量研究中的 39.7%和 10.0%。在两项研究中,与 PBO 相比,SHP465 MAS 达到反应和缓解的时间都更长(所有名义对数秩检验 < 0.0001)。
这些分析表明,与 PBO 相比,SHP465 MAS 与成人 ADHD 的更高反应和缓解率相关,与反应和缓解的时间也名义上有利于 SHP465 MAS。