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首页> 外文期刊>Brain and Behavior >Adjunctive brexpiprazole in patients with major depressive disorder and anxiety symptoms: an exploratory study
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Adjunctive brexpiprazole in patients with major depressive disorder and anxiety symptoms: an exploratory study

机译:患有严重抑郁症和焦虑症患者的辅助性brexpiprazole:一项探索性研究

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Abstract Background Major depressive disorder (MDD) with concurrent anxiety symptoms may signal a difficult-to-treat patient. Brexpiprazole is a serotonin?¢????dopamine activity modulator: a partial agonist at 5-HT 1A and dopamine D 2 receptors at similar potency, and an antagonist at 5-HT 2A and noradrenaline alpha 1B/2C receptors. The objective of this Phase IIIb study was to explore effectiveness, safety, and tolerability of brexpiprazole adjunctive to antidepressant (ADT) monotherapy in patients with MDD and anxiety symptoms (NCT02013531). Methods Patients with MDD, Hamilton Anxiety Rating Scale (HAM-A) total score ?¢???¥ 20, and inadequate response to current ADT received open-label brexpiprazole 1?¢????3 mg day ?¢????1 (target dose 2 mg day ?¢????1 ) + ADT for 6 weeks. Efficacy endpoints included change from baseline at Week 6 in Montgomery?¢????????sberg Depression Rating Scale (MADRS) total score, HAM-A total score, and Sheehan Disability Scale (SDS). Safety and tolerability assessments included adverse events (AEs). Results Of 37 participants enrolled, 32 (86.5%) completed the study. Baseline mean ( SD ) MADRS total score was 30.1 (5.1); mean HAM-A total score was 26.9 (5.0). Improvements from baseline were observed at Week 6 for least squares mean change in MADRS total score (?¢????19.6, p < .0001 vs. baseline), HAM-A total score (?¢????17.8, p < .0001) and mean ( SD ) SDS mean score [?¢????3.6 (2.6)]. Brexpiprazole was well tolerated. The most frequent treatment-emergent AEs were increased appetite (13.5%) and diarrhea, dry mouth, and dizziness (all 10.8%). Conclusions These open-label results support the anxiolytic effects of adjunctive brexpiprazole in the treatment of patients with MDD.
机译:摘要背景伴有焦虑症状的重度抑郁症(MDD)可能预示着难以治疗的患者。布雷哌拉唑是5-羟色胺β-多巴胺活性调节剂:在5-HT 1A和多巴胺D 2受体处具有相似效力的部分激动剂,在5-HT 2A和去甲肾上腺素α1B / 2C受体处具有拮抗剂。这项IIIb期研究的目的是探讨在患有MDD和焦虑症的患者中使用抗抑郁药(ADT)辅助治疗的brexpiprazole的有效性,安全性和耐受性(NCT02013531)。方法MDD,汉密尔顿焦虑量表(HAM-A)总分≥20且对当前ADT反应不足的患者接受开放标签的brexpiprazole 1 mg每天3 mg。 ≥1(目标剂量为每天2mg,≥1)+ ADT持续6周。功效终点包括蒙哥马利沙伯抑郁量表(MADRS)总分,HAM-A总分和希恩残疾量表(SDS)在第6周时自基线的变化。安全性和耐受性评估包括不良事件(AE)。结果共有37位参与者参加,其中32位(86.5%)完成了研究。基线平均(SD)MADRS总分是30.1(5.1);平均HAM-A总分是26.9(5.0)。在第6周观察到MADRS总得分的最小二乘均方差(相对于基线,均方差为19.6,p <.0001),HAM-A总得分(均方根为17.8,p <.0001)和SDS平均值(SD)平均值[3.6(2.6)]。 Brexpiprazole的耐受性良好。出现治疗最频繁的不良事件是食欲增加(13.5%)和腹泻,口干,头晕(所有发生率为10.8%)。结论这些开放性研究结果支持辅助性布立哌唑在MDD患者中的抗焦虑作用。

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