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首页> 外文期刊>Journal of psychiatric research >Efficacy and tolerability of the novel triple reuptake inhibitor amitifadine in the treatment of patients with major depressive disorder: A randomized, double-blind, placebo-controlled trial
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Efficacy and tolerability of the novel triple reuptake inhibitor amitifadine in the treatment of patients with major depressive disorder: A randomized, double-blind, placebo-controlled trial

机译:新型三重摄取抑制剂阿米替丁对重度抑郁症患者的疗效和耐受性:一项随机,双盲,安慰剂对照试验

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Amitifadine (EB-1010, formerly DOV 21,947) is a serotonin-preferring triple reuptake inhibitor with a relative potency to inhibit serotonin, norepinephrine, and dopamine uptake of ~1:2:8, respectively. This 6-week, multicenter, randomized, double-blind, parallel, placebo-controlled study evaluated the efficacy and tolerability of amitifadine in 63 patients with major depressive disorder. Eligible patients (17-item Hamilton Depression Rating Scale [HAMD-17] ≥ 22 at baseline) were randomized to amitifadine 25 mg twice daily (BID) for 2 weeks, then 50 mg BID for 4 weeks or placebo. Mean baseline scores in the modified intent-to-treat population (n = 56) were 31.4 for the Montgomery-?sberg Depression Rating Scale (MADRS), 29.6 for the HAMD-17, and 25.4 for the Derogatis Interview for Sexual Functioning - Self Report (DISF-SR). At the end of the 6-week double-blind treatment, estimated least squares mean change from baseline (mixed-model repeated measures [MMRM]) in MADRS total score was statistically significantly superior for amitifadine compared to placebo (18.2 vs. 22.0; p = 0.028), with an overall statistical effect size of -0.601 (Cohen's d). Amitifadine also was statistically significantly superior to placebo (p = 0.03) for the Clinical Global Impression of Change - Improvement. An anhedonia factor score grouping of MADRS Items 1 (apparent sadness), 2 (reported sadness), 6 (concentration difficulties), 7 (lassitude), and 8 (inability to feel) demonstrated a statistically significant difference in favor of amitifadine compared to placebo (p = 0.049). No differences were observed between treatments in DISF-SR scores. Amitifadine was well-tolerated. Two patients on each treatment discontinued the study early due to adverse events; however, no serious adverse events were reported. This initial clinical trial in patients with severe major depression demonstrated significant antidepressant activity with amitifadine, including attenuating symptoms of anhedonia, and a tolerability profile that was comparable to placebo. The efficacy and tolerability of amitifadine for major depressive disorder are being investigated in additional clinical trials.
机译:Amitifadine(EB-1010,前身为DOV 21,947)是5-羟色胺优先的三重再摄取抑制剂,相对抑制5-羟色胺,去甲肾上腺素和多巴胺摄取的效价分别约为1:2:8。这项为期6周的多中心,随机,双盲,平行,安慰剂对照研究评估了Amitifadine在63例重度抑郁症患者中的疗效和耐受性。符合条件的患者(基线时有17个项的汉密尔顿抑郁量表[HAMD-17]≥22)随机分为阿米替丁25毫克每天两次(BID),持续2周,然后50毫克BID,持续4周或安慰剂。改良的意向性治疗人群(n = 56)的平均基线评分为31.4(蒙哥马利-西斯伯格抑郁量表),HAMD-17的29.6和Derogatis面试的性功能-自我25.4。报告(DISF-SR)。在为期6周的双盲治疗结束时,与安慰剂相比,阿米替丁的MADRS总评分与基线的最低最小均方差(混合模型重复测量[MMRM])在统计学上明显优于安慰剂组(分别为18.2和22.0; P = 0.028),总体统计效果大小为-0.601(Cohen d)。在临床上对变化的整体印象-改善方面,阿米替丁在统计学上也显着优于安慰剂(p = 0.03)。 MADRS项目1(明显的悲伤),2(报告的悲伤),6(注意力不集中),7(疲倦)和8(无法感觉)的无感因素得分分组显示,与安慰剂相比,阿米替丁具有统计学意义上的显着差异(p = 0.049)。在DISF-SR评分之间未观察到差异。阿米替丁的耐受性良好。每次治疗中有两名患者因不良事件而中止了研究。但是,没有严重的不良反应的报道。这项针对严重重度抑郁症患者的初始临床试验表明,阿米替丁具有显着的抗抑郁活性,包括减轻了快感不足的症状,其耐受性与安慰剂相当。阿米替丁对重度抑郁症的疗效和耐受性正在其他临床试验中进行研究。

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