CTRI/2009/091/000647已完成3 期
A Randomized, 6-Week, Double-Blind, Placebo-Controlled, Fixed-Flexible Dose, Parallel-Group Study of Lurasidone for the Treatment of Bipolar I Depression
Dainippon Sumitomo Pharma America Inc0 个研究点目标入组 0 人开始时间: 待定最近更新:
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 发起方
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
入选标准
- •Subject is diagnosed with bipolar I disorder, most resent episode depressed
- •Subject must have a lifetime history of at least one bipolar manic or mixed episode
排除标准
- •History of nonresponse to an adequate (6-week) trial of three or more antidepressants (with or without mood stabilizers) during the current episode
- •Subject has been hospitalized for a manic or mixed episode within 60 days prior to randomization
- •Imminent risk of suicide or injury to self, others, or property
研究者
相似试验
进行中（未招募）
不适用
A Randomized, 6-Week, Double-Blind, Placebo-Controlled, Flexible-Dose, Parallel-Group Study of Lurasidone Adjunctive to Lithium or Divalproex for the Treatment of Bipolar I DepressioEUCTR2008-007482-23-DESunovion Pharmaceuticals Inc.340
进行中（未招募）
1 期
uradisone for the treatment of depression disorderEUCTR2012-004132-33-GBSunovion Pharmaceuticals Inc.209
进行中（未招募）
1 期
A 6-Week Study of Lurasidone Adjunctive to Lithium or Divalproex for the Treatment of Bipolar DepressioBipolar depressionMedDRA version: 14.1Level: LLTClassification code 10004936Term: Bipolar depressionSystem Organ Class: 10037175 - Psychiatric disordersEUCTR2008-007482-23-CZSunovion Pharmaceuticals, Inc.340
进行中（未招募）
1 期
A Randomized, 6-Week, Double-Blind, Placebo-Controlled, Flexible-Dose, Parallel-Group Study of Lurasidone Adjunctive to Lithium or Divalproex for the Treatment of Bipolar I DepressioBipolar depressionMedDRA version: 9.1Level: LLTClassification code 10004936Term: Bipolar depressionEUCTR2008-007482-23-FRDainippon Sumitomo Pharma America Inc.340
已完成
3 期
A study to evaluate the efficacy of Lurasidone Adjunctive to Lithium or Divalproex for the Treatment of Bipolar I Depression in Subjects Demonstrating Non-Response to Treatment with Lithium or Divalproex AloneCTRI/2011/06/001808Sunovion Pharmaceuticals Inc340