首页> 美国卫生研究院文献>Springer Open Choice >Long-Term (1 Year) Safety and Efficacy of Methylphenidate Modified-Release Long-Acting Formulation (MPH-LA) in Adults with Attention-Deficit Hyperactivity Disorder: A 26-Week Flexible-Dose Open-Label Extension to a 40-Week Double-Blind Randomised Placebo-Controlled Core Study
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Long-Term (1 Year) Safety and Efficacy of Methylphenidate Modified-Release Long-Acting Formulation (MPH-LA) in Adults with Attention-Deficit Hyperactivity Disorder: A 26-Week Flexible-Dose Open-Label Extension to a 40-Week Double-Blind Randomised Placebo-Controlled Core Study

机译:患有注意力缺陷多动障碍的成年人的哌醋甲酯修饰释放长效制剂(MPH-LA)的长期(1年)安全性和有效性:26周灵活剂量开放标签扩展到40-周双盲随机安慰剂对照核心研究

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摘要

IntroductionPreviously, in a 40-week, randomised, double-blind, placebo-controlled core study comprising three phases (9-week dose confirmation, 5-week open-labeldose optimisation and 6-month maintenance of effect) in adults with attention-deficit/hyperactivity disorder (ADHD), methylphenidate modified-release long-acting formulation (MPH-LA) at 40–80 mg/day controlled ADHD symptoms as well as decreased functional impairment with a good tolerability profile (). Here, we report the long-term efficacy and safety from a 26-week, open-label extension phase of the same study ().
机译:引言此前,在一项注意力缺乏的成年人中,一项为期40周,随机,双盲,安慰剂对照的核心研究包括三个阶段(9周剂量确认,5周开放标签剂量优化和6个月维持疗效) /多动障碍(ADHD),哌醋甲酯缓释长效剂(MPH-LA)以40-80 mg / day的剂量控制ADHD症状,并降低功能障碍,具有良好的耐受性()。在这里,我们报告了同一项研究的26周开放标签扩展期的长期疗效和安全性()。

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