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阿立哌唑辅助治疗重度抑郁症患者:一项随机、双盲、安慰剂对照的3期研究。

Adjunctive Cariprazine for the Treatment of Patients With Major Depressive Disorder: A Randomized, Double-Blind, Placebo-Controlled Phase 3 Study.

作者信息

Sachs Gary S, Yeung Paul P, Rekeda Ludmyla, Khan Arifulla, Adams Julie L, Fava Maurizio

机构信息

Department of Psychiatry, Harvard Medical School, and Massachusetts General Hospital, Boston (Sachs, Fava); Signant Health, Blue Bell, Penn. (Sachs); AbbVie, Madison, N.J. (Yeung, Rekeda, Adams); Northwest Clinical Research Center, Bellevue, Wash. (Khan).

出版信息

Am J Psychiatry. 2023 Mar 1;180(3):241-251. doi: 10.1176/appi.ajp.20220504. Epub 2023 Feb 15.

Abstract

OBJECTIVE

The purpose of this study was to investigate the efficacy of cariprazine, a dopamine D-preferring D/D and serotonin 5-HT receptor partial agonist, as adjunctive therapy for patients with major depressive disorder and nonresponse to at least one antidepressant monotherapy.

METHODS

In this double-blind placebo-controlled study, adults with major depressive disorder and inadequate response to antidepressants alone were randomized in a 1:1:1 ratio to placebo, cariprazine at 1.5 mg/day, or cariprazine at 3.0 mg/day. The primary outcome was change from baseline to week 6 in total score on the Montgomery-Åsberg Depression Rating Scale (MADRS). Least-squares mean differences were estimated in the modified intent-to-treat (mITT) population using a mixed-effects model for repeated measures with adjustment for multiple comparisons.

RESULTS

The mITT population comprised 751 patients (placebo: N=249; cariprazine 1.5 mg/day: N=250; cariprazine 3.0 mg/day: N=252). At week 6, the mean reduction from baseline in MADRS total score was significantly greater with cariprazine 1.5 mg/day than with placebo (-14.1 vs. -11.5) but not with cariprazine 3.0 mg/day (-13.1). Significant differences between the cariprazine 1.5 mg/day and placebo groups were also observed at weeks 2 and 4. Meeting the MADRS response criteria was significantly more likely among patients receiving cariprazine 1.5 mg/day than placebo (44.0% vs. 34.9%); remission rates were not significantly different among groups. Common treatment-emergent adverse events (≥5% in either cariprazine group and twice the placebo rate) were akathisia and nausea.

CONCLUSIONS

Adjunctive cariprazine at 1.5 mg/day demonstrated efficacy in reducing depressive symptoms in adults with major depressive disorder and inadequate response to antidepressants alone. Cariprazine was generally well tolerated, with a safety profile that was consistent with previous findings.

摘要

目的

本研究旨在探讨卡利拉嗪(一种优先作用于多巴胺D3/D2受体和5-羟色胺5-HT受体的部分激动剂)作为辅助治疗对重度抑郁症且对至少一种抗抑郁单药治疗无反应的患者的疗效。

方法

在这项双盲安慰剂对照研究中,患有重度抑郁症且仅使用抗抑郁药反应不佳的成年人按1:1:1的比例随机分为安慰剂组、1.5毫克/天卡利拉嗪组或3.0毫克/天卡利拉嗪组。主要结局是蒙哥马利-阿斯伯格抑郁评定量表(MADRS)总分从基线到第6周的变化。使用重复测量的混合效应模型并对多重比较进行调整,在改良意向性治疗(mITT)人群中估计最小二乘均值差异。

结果

mITT人群包括751名患者(安慰剂组:N = 249;1.5毫克/天卡利拉嗪组:N = 250;3.0毫克/天卡利拉嗪组:N = 252)。在第6周时,1.5毫克/天卡利拉嗪组MADRS总分较基线的平均降低幅度显著大于安慰剂组(-14.1对-11.5),但3.0毫克/天卡利拉嗪组则不然(-13.1)。在第2周和第4周时,1.5毫克/天卡利拉嗪组与安慰剂组之间也观察到显著差异。接受1.5毫克/天卡利拉嗪治疗的患者达到MADRS反应标准的可能性显著高于安慰剂组(44.0%对34.9%);各组之间的缓解率无显著差异。常见的治疗中出现的不良事件(在任一卡利拉嗪组中≥5%且为安慰剂组发生率的两倍)为静坐不能和恶心。

结论

1.5毫克/天的卡利拉嗪辅助治疗对重度抑郁症且仅使用抗抑郁药反应不佳的成年人具有减轻抑郁症状的疗效。卡利拉嗪总体耐受性良好,安全性与先前研究结果一致。

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