AVIDA, Newport Beach, CA, USA.
Center for Psychiatry and Behavioral Medicine Inc., Las Vegas, NV, USA.
J Atten Disord. 2020 Feb;24(3):373-383. doi: 10.1177/1087054716672335. Epub 2016 Oct 17.
The aim of this study is to assess the onset and duration of efficacy of multilayer-release methylphenidate (PRC-063) over 16 hr compared with placebo in adults with ADHD using the simulated adult workplace environment. After dose-optimization with PRC-063, participants entered a double-blind, placebo-controlled, crossover phase. Primary outcome measure was the Permanent Product Measure of Performance (PERMP) total score measured pre-dose and from 1 to 16 hr post-dose. Of the 59 randomized participants, 45 participants completed the study. While receiving PRC-063, adults had greater mean PERMP total scores across all time points compared with placebo (268.7 ± 11.24 vs. 255.6 ± 10.87; = .0064). Common adverse events were decreased appetite, headache, and insomnia. There was no significant impact on overall sleep quality ( = .9542). PRC-063 significantly improved PERMP scores with an onset within 1 hr post-dose, and maintained improvement throughout the 16 hr post-dose study period compared with placebo in adults with ADHD.
本研究旨在评估与安慰剂相比,在模拟成人工作环境中,多层层析释放哌甲酯(PRC-063)在 ADHD 成人患者中 16 小时内的疗效起始时间和持续时间。在经过 PRC-063 的剂量优化后,参与者进入了双盲、安慰剂对照、交叉阶段。主要的疗效评估指标是在给药前和给药后 1 至 16 小时内测量的永久性绩效测量(PERMP)总分。在随机的 59 名参与者中,有 45 名完成了研究。在接受 PRC-063 治疗时,与安慰剂相比,成年人在所有时间点的 PERMP 总分都有显著提高(268.7±11.24 与 255.6±10.87;=.0064)。常见的不良反应包括食欲减退、头痛和失眠。但对整体睡眠质量没有显著影响(=.9542)。PRC-063 显著改善了 PERMP 评分,其起效时间在给药后 1 小时内,与安慰剂相比,在 ADHD 成人患者中,在 16 小时的给药后研究期间内维持了改善。