跳至主要内容
临床试验/NCT03249376
NCT03249376已完成3 期

A Phase 3, Randomized, Double-Blind, Placebo-Controlled, Multi-Center Study to Assess the Efficacy and Safety of Lumateperone Monotherapy in the Treatment of Patients With Major Depressive Episodes Associated With Bipolar I or Bipolar II Disorder (Bipolar Depression) Conducted Globally

Intra-Cellular Therapies, Inc.1 个研究点 分布在 1 个国家目标入组 381 人开始时间: 2017年11月27日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
已完成
入组人数
381
试验地点
1
主要终点
Change From Baseline in Montgomery-Åsberg Depression Rating Scale (MADRS) Total Score

研究概览

简要总结

The study will evaluate the efficacy and safety of ITI-007 in a randomized, double-blind, parallel-group, placebo-controlled, multi-center study in patients diagnosed with Bipolar I or Bipolar II disorder having a major depressive episode.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • male or female subjects of any race, ages 18-75 inclusive, with a clinical diagnosis of Bipolar I or Bipolar II disorder
  • experiencing a current major depressive episode
  • able to provide written informed consent

排除标准

  • any female subject who is pregnant or breast-feeding
  • any subject judged to be medically inappropriate for study participation

研究组 & 干预措施

Lumateperone

Experimental

Lumateperone 42 mg (ITI-007 60 mg tosylate) administered once daily every evening for 6 weeks

干预措施: Lumateperone (Drug)

Placebo

Placebo Comparator

Placebo administered once daily every evening for 6 weeks

干预措施: Placebo (Other)

结局指标

主要结局

Change From Baseline in Montgomery-Åsberg Depression Rating Scale (MADRS) Total Score

时间窗: Baseline to Day 43

The Montgomery-Åsberg Depression Rating Scale (MADRS) is a clinician-rated 10 item scale to assess depressive symptoms. Each item is rated on a 7-point scale from 0-6. The total score ranges from 0 to 60 with a higher score indicating increased severity of depressive symptoms.

次要结局

  • Change From Baseline in Clinical Global Impression Scale, Bipolar Version (CGI-BP-S) Total Score(Baseline to Day 43)
  • Change From Baseline in Quality of Life Enjoyment and Satisfaction Questionnaire - Short Form (Q-LES-Q-SF) Percent Score(Baseline to Day 43)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

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