Yatham Lakshmi N, Vieta Eduard, McIntyre Roger S, Jain Rakesh, Patel Mehul, Earley Willie
University Hospital-Detwiller Pavilion 2883, 2255 Wesbrook Mall, Vancouver, BC, V6T 2A1, Canada.
Department of Psychiatry, University of British Columbia, Vancouver, British Columbia, Canada.
Prim Care Companion CNS Disord. 2020 Sep 17;22(5):20m02611. doi: 10.4088/PCC.20m02611.
Bipolar disorder is a complex mood disorder characterized by a chronic and subtle course of fluctuating manic/hypomanic and depressive symptoms. Cariprazine, a dopamine D₃-preferring D₃/D₂ receptor partial agonist with serotonin 5-HT1A receptor partial agonist and serotonin 5-HT2A antagonist properties, is approved to treat manic and depressive episodes of bipolar disorder. Post hoc analyses evaluated efficacy across symptoms in bipolar depression.
Pooled data were analyzed from 3 phase 2 or 3, randomized, double-blind, placebo-controlled studies of adults with bipolar disorder and a major depressive episode. Mean change from baseline to week 6 in Montgomery-Asberg Depression Rating Scale (MADRS) total score and individual item scores were analyzed in individual dose groups (1.5 mg/d, 3 mg/d) and overall cariprazine (1.5-3 mg/d). Pooled safety was evaluated via adverse events.
A significantly greater difference in mean change from baseline in MADRS total score was seen for each cariprazine dose group versus placebo (least squares mean difference vs placebo: 1.5-3 mg/d = -2.6, 1.5 mg/d = -2.8, 3 mg/d = -2.4) (P < .001 all). Significant differences versus placebo were seen on all individual MADRS items except inner tension for the overall cariprazine group (P < .05). Cariprazine was generally well tolerated.
Cariprazine demonstrated broad efficacy across symptoms of depression in bipolar disorder. In previous post hoc analyses, cariprazine also demonstrated broad efficacy across manic symptoms, suggesting that it is effective across the wide range of symptoms on the bipolar spectrum. A 1.5-mg/d starting dose and slow titration resulted in lower rates of some adverse events in the bipolar depression studies versus the mania studies.
ClinicalTrials.gov identifiers: NCT01396447, NCT02670538, NCT02670551.
双相情感障碍是一种复杂的心境障碍,其特征为慢性且细微的躁狂/轻躁狂和抑郁症状波动病程。卡立普嗪是一种对多巴胺D₃受体具有优先亲和力的D₃/D₂受体部分激动剂,同时具有5-羟色胺5-HT1A受体部分激动剂和5-羟色胺5-HT2A拮抗剂特性,已被批准用于治疗双相情感障碍的躁狂和抑郁发作。事后分析评估了双相抑郁各症状的疗效。
汇总分析了3项2期或3期随机、双盲、安慰剂对照研究的数据,这些研究针对患有双相情感障碍且伴有重度抑郁发作的成年人。分析了各个剂量组(1.5毫克/天、3毫克/天)和整个卡立普嗪组(1.5 - 3毫克/天)从基线到第6周蒙哥马利-艾斯伯格抑郁量表(MADRS)总分及各单项得分的平均变化。通过不良事件评估汇总安全性。
各卡立普嗪剂量组与安慰剂相比,MADRS总分从基线的平均变化差异显著更大(最小二乘均值差异与安慰剂相比:1.5 - 3毫克/天 = -2.6,1.5毫克/天 = -2.8,3毫克/天 = -2.4)(所有P <.001)。整个卡立普嗪组除内心紧张外,所有MADRS单项与安慰剂相比均有显著差异(P <.05)。卡立普嗪总体耐受性良好。
卡立普嗪在双相情感障碍的抑郁症状方面显示出广泛疗效。在先前的事后分析中,卡立普嗪在躁狂症状方面也显示出广泛疗效,这表明它在双相情感谱的广泛症状范围内均有效。与躁狂症研究相比,双相抑郁症研究中1.5毫克/天的起始剂量和缓慢滴定导致某些不良事件发生率较低。
ClinicalTrials.gov标识符:NCT01396447、NCT02670538、NCT02670551。