Adjunctive brexpiprazole in patients with major depressive disorder and anxiety symptoms: post hoc analyses of three placebo-controlled studies

被引:15
|
作者
Thase, Michael E. [1 ,2 ]
Weiller, Emmanuelle [3 ]
Zhang, Peter [4 ]
Weiss, Catherine [5 ]
McIntyre, Roger S. [6 ]
机构
[1] Univ Penn, Dept Psychiat, Perelman Sch Med, 3535 Market St,Suite 670, Philadelphia, PA 19104 USA
[2] Philadelphia Vet Affairs Med Ctr, Philadelphia, PA USA
[3] H Lundbeck & Co AS, Med Affairs, Copenhagen, Denmark
[4] Otsuka Pharmaceut Dev & Commercializat Inc, Biostat Dept, Princeton, NJ USA
[5] Otsuka Pharmaceut Dev & Commercializat Inc, Global Med Affairs, Princeton, NJ USA
[6] Univ Toronto, Univ Hlth Network, Mood Disorders Psychopharmacol Unit, Toronto, ON, Canada
关键词
depression; double-blind method; random allocation; antidepressants; antipsychotics; ANXIOUS DISTRESS SPECIFIER; RELEASE QUETIAPINE FUMARATE; INADEQUATE RESPONSE; ANTIDEPRESSANT THERAPY; RATING-SCALE; EFFICACY; PHASE-3; SAFETY; MG;
D O I
10.2147/NDT.S185815
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective: Episodes of major depressive disorder (MDD) characterized by high levels of anxiety symptoms are less likely to respond to some forms of antidepressant treatment (ADT). This report examines the effects of adjunctive brexpiprazole on depressive symptoms among patients with MDD and anxiety symptoms. Materials and methods: This was a post hoc analysis of 1,171 patients from the 6-week, randomized, double-blind phases of three studies in adults with MDD and inadequate response to ADTs (NCT01360645,NCT01360632,NCT02196506). Data were pooled for brexpiprazole 2-3 mg/day and for placebo (adjunct to ADT). Montgomery-Asberg Depression Rating Scale Total score changes were assessed in subgroups of patients with and without anxious distress (based on proxies for the Diagnosiie and Siaiisiical Manual of Menial Disorders, Fifth Edition criteria) and anxious depression (defined as a Hamilton Depression Rating Scale Anxiety/somatization factor score of >= 7) Safety was assessed by the incidence of treatment-emergent adverse: events (TEAEs). Results: Benefits were seen for adjunctive brexpiprazole (compared with adjunctive placebo) in both anxiety definition subgroups. For patients with anxious distress, the least squares mean difference (95% CI) at week 6 was -3.00 (-4.29, -1.71; P<0.0001) and, for those without anxious distress, was -1.38 (-2.71, -0.05; P=0.043). For patients with anxious depression, the difference was-2.19 (-3.60, -0.78; P=0.0023), compared with -2.34 (-3.58,-1.10; P=0.0002) for those without anxious depression. The most common TEAEs among patients with anxiety symptoms receiving ADT + brexpiprazole were akathisia, headache, restlessness, somnolence, and weight increase. There were no clinically meaningful differences in the rates of these TEAEs according to the presence or absence of anxiety symptoms. Conclusion: Adjunctive brexpiprazole 2-3 mg/day may be efficacious in reducing depressive symptoms, and was well tolerated, in patients with clinically relevant anxiety symptoms.
引用
收藏
页码:37 / 45
页数:9
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