Eli Lilly and Company, Lilly Corporate Center, Indianapolis, IN, 46285, United States; Indiana University School of Medicine, Department of Psychiatry, Indianapolis, IN, 46202, United States.
Eli Lilly and Company, Lilly Corporate Center, Indianapolis, IN, 46285, United States.
J Affect Disord. 2014;167:215-23. doi: 10.1016/j.jad.2014.06.006. Epub 2014 Jun 14.
This phase 2 study examined the efficacy and tolerability of edivoxetine, a highly selective norepinephrine reuptake inhibitor, as an adjunctive treatment for patients with major depressive disorder (MDD) who have a partial response to selective serotonin reuptake inhibitor (SSRI) treatment.
Study design consisted of double-blind, 10-week therapy of adjunctive edivoxetine (6-18 mg once daily) or adjunctive placebo with SSRI. Inclusion/entry criteria included partial response to current SSRI by investigator opinion and a GRID 17-item Hamilton Rating Scale for Depression (HAMD17) total score ≥16. The primary efficacy measure was the Montgomery-Asberg Depression Rating Scale (MADRS). Safety measures included treatment-emergent adverse events (TEAE) and vital signs.
For the primary evaluable population (n=63 for adjunctive edivoxetine and n=68 for adjunctive placebo), the treatment groups did not differ significantly on the primary outcome of change from baseline to week 8 in the MADRS total score; the effect size of edivoxetine treatment was 0.26. Significant treatment differences, favoring adjunctive edivoxetine (p≤.05), were shown for improvements in role functioning and the functional impact of fatigue. For the adjunctive edivoxetine randomized group (N=111), the most frequent TEAEs were hyperhidrosis (7.2%), nausea (7.2%), erectile dysfunction (6.3%) and testicular pain (6.3%). Hemodynamic changes were observed in blood pressure and pulse rate between treatment groups.
Study was underpowered for an alpha 2-sided 0.05 significance level for the primary outcome.
For patients with MDD who had a partial response to SSRIs, adjunctive edivoxetine treatment was not statistically superior to adjunctive placebo on the primary outcome measure. However, pending further study, improved functioning and remission rate suggest a potential role for edivoxetine for patients with depression.
这项 2 期研究评估了高度选择性去甲肾上腺素再摄取抑制剂依度沙班作为辅助治疗对接受选择性 5-羟色胺再摄取抑制剂(SSRI)治疗部分缓解的重度抑郁症(MDD)患者的疗效和耐受性。
研究设计包括双盲、为期 10 周的依度沙班(每日一次,6-18mg)或 SSRI 辅助安慰剂治疗。纳入/入组标准包括研究者认为当前 SSRI 部分缓解和 GRID 17 项汉密尔顿抑郁量表(HAMD17)总分≥16。主要疗效指标为蒙哥马利-阿斯伯格抑郁评定量表(MADRS)。安全性指标包括治疗中出现的不良事件(TEAE)和生命体征。
对于主要可评估人群(依度沙班辅助治疗组 n=63,安慰剂辅助治疗组 n=68),MADRS 总分从基线到第 8 周的变化在主要结局上两组无显著差异;依度沙班治疗的效应量为 0.26。在角色功能和疲劳的功能影响方面,辅助依度沙班治疗有显著的治疗差异(p≤.05),这对患者有益。对于依度沙班辅助随机治疗组(N=111),最常见的 TEAEs 为多汗症(7.2%)、恶心(7.2%)、勃起功能障碍(6.3%)和睾丸疼痛(6.3%)。治疗组之间观察到血压和脉搏率的血液动力学变化。
对于主要结局,该研究的效力不足以达到双侧 0.05 的α水平。
对于接受 SSRI 治疗部分缓解的 MDD 患者,辅助依度沙班治疗在主要疗效指标上与辅助安慰剂相比无统计学优势。然而,在进一步研究之前,功能改善和缓解率提示依度沙班对抑郁症患者可能有潜在作用。