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卡利拉嗪治疗双相抑郁症的随机双盲安慰剂对照 3 期研究。

Cariprazine Treatment of Bipolar Depression: A Randomized Double-Blind Placebo-Controlled Phase 3 Study.

机构信息

Allergan, Madison, N.J. (Earley, Burgess, Rekeda, Dickinson); Gedeon Richter, Budapest, Hungary (Szatmári, Németh); the Mood Disorders Psychopharmacology Unit, University Health Network, Toronto (McIntyre); the Department of Psychiatry, Harvard Medical School, and the Bipolar Clinic and Research Program, Massachusetts General Hospital, Boston (Sachs); and the Department of Psychiatry, University of British Columbia, Vancouver (Yatham).

出版信息

Am J Psychiatry. 2019 Jun 1;176(6):439-448. doi: 10.1176/appi.ajp.2018.18070824. Epub 2019 Mar 8.

Abstract

OBJECTIVE

Cariprazine, a dopamine D/D and 5-HT receptor partial agonist, was found to be effective in treating bipolar I depression in a previous phase 2 study. This phase 3 study further assessed the efficacy, safety, and tolerability of cariprazine in bipolar I depression.

METHODS

In a double-blind placebo-controlled study, adult participants (18-65 years old) who met DSM-5 criteria for bipolar I disorder and a current depressive episode were randomly assigned to receive placebo (N=158) or cariprazine at 1.5 mg/day (N=157) or 3.0 mg/day (N=165). The primary and secondary efficacy parameters were changes from baseline to week 6 in Montgomery-Åsberg Depression Rating Scale (MADRS) score and Clinical Global Impressions severity (CGI-S) score, respectively. Least squares mean differences were estimated using a mixed model for repeated measures, and p values were adjusted for multiplicity.

RESULTS

Both dosages of cariprazine were significantly more effective than placebo in improving depressive symptoms (reducing MADRS total score); the least squares mean differences were -2.5 (95% CI=-4.6, -0.4) for cariprazine at 1.5 mg/day and -3.0 (95% CI=-5.1, -0.9) for cariprazine at 3.0 mg/day. Both cariprazine dosages were associated with lower CGI-S scores compared with placebo, but the differences did not reach statistical significance after adjustment for multiplicity (least squares mean difference, -0.2 [95% CI=-0.5, 0.0] for the 1.5 mg/day group and -0.3 [95% CI=-0.5, 0.0] for the 3.0 mg/day group). Common treatment-emergent adverse events (in at least 5% of participants in either cariprazine treatment group and twice the rate of the placebo group) were nausea, akathisia, dizziness, and sedation. Mean changes in weight and metabolic parameters were relatively small and comparable across groups.

CONCLUSIONS

Cariprazine, at both 1.5 mg/day and 3.0 mg/day, was effective, generally well tolerated, and relatively safe in reducing depressive symptoms in adults with bipolar I depression.

摘要

目的

卡利拉嗪是一种多巴胺 D/D 和 5-HT 受体部分激动剂,在之前的一项 2 期研究中已被证明对治疗双相 I 型抑郁症有效。这项 3 期研究进一步评估了卡利拉嗪在双相 I 型抑郁症中的疗效、安全性和耐受性。

方法

在一项双盲安慰剂对照研究中,符合 DSM-5 双相 I 障碍标准且当前处于抑郁发作的成年参与者(18-65 岁)被随机分配接受安慰剂(N=158)或卡利拉嗪 1.5mg/天(N=157)或 3.0mg/天(N=165)。主要和次要疗效参数分别为从基线到第 6 周时蒙哥马利-阿斯伯格抑郁评定量表(MADRS)评分和临床总体印象严重程度(CGI-S)评分的变化。使用重复测量混合模型估计最小二乘均数差异,p 值经多重性调整。

结果

卡利拉嗪两种剂量均明显优于安慰剂,可改善抑郁症状(降低 MADRS 总分);卡利拉嗪 1.5mg/天的最小二乘均数差异为-2.5(95%CI=-4.6,-0.4),卡利拉嗪 3.0mg/天的最小二乘均数差异为-3.0(95%CI=-5.1,-0.9)。与安慰剂相比,卡利拉嗪两种剂量均与 CGI-S 评分降低相关,但经多重性调整后差异无统计学意义(1.5mg/天组的最小二乘均数差异为-0.2[95%CI=-0.5,0.0],3.0mg/天组为-0.3[95%CI=-0.5,0.0])。常见的治疗相关不良事件(至少在卡利拉嗪治疗组中发生 5%的参与者,且发生率是安慰剂组的两倍)为恶心、静坐不能、头晕和镇静。体重和代谢参数的平均变化较小,且各组之间相当。

结论

卡利拉嗪 1.5mg/天和 3.0mg/天均有效,总体耐受性良好,在降低双相 I 型抑郁症成人的抑郁症状方面相对安全。

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