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临床试验/NCT00374920
NCT00374920已完成2 期

A Multicenter, Double Blind, Placebo-Controlled Study to Evaluate the Safety and Efficacy of MEM 1003 for the Treatment of Patients With Bipolar I Disorder Suffering Acute Manic or Mixed Episodes

Memory Pharmaceuticals21 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2006年9月最近更新:
适应症
相关药物

试验速览

阶段
2 期
状态
已完成
入组人数
60
试验地点
21
主要终点
Response rate at Day 21

研究概览

简要总结

The purpose of this study is to establish the potential of MEM 1003 as a safe and effective treatment for patients with an acute manic or mixed episode of bipolar disorder.

详细描述

Bipolar affective disorder is one of the most common, severe, and persistent mental illnesses. It is characterized by periods of deep, prolonged, and profound depressions that alternate with periods of excessively elevated and/or irritable mood (mania). The pathophysiology of bipolar disorder is complex, and can include an inheritable component, administration of antidepressant medications, behavioral sensitization processes, and neuronal calcium dysregulation that leads to apoptosis of critical brain circuitry that regulates emotion. Addressing the dysregulation in calcium levels in the central nervous system by administering compounds such as MEM 1003 may have the potential for altering the cyclical course or progression of bipolar disorder.

MEM 1003 is the (+)-enantiomer of a dihydropyridine that has been optimized for central nervous system activity. It inhibits L-type Ca2+ channels and within the anticipated human dosing range has more benign cardiovascular effects than other DHP L-Type calcium channel modulators.

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
Double

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • bipolar I disorder with acute manic or mixed episode, with or without psychotic features
  • YMRS score of at least 20
  • history of at least one previous manic or mixed episode requiring treatment in the last 10 years

排除标准

  • history of failing to respond to treatment with two or more adequate trials of approved anti-manic medications for the current episode
  • Axis I or Axis II disorder (other than bipolar I disorder) that requires treatment or has been the primary subject of treatment in the past 3 months
  • defined substance abuse or dependency within the 3 months
  • schizophrenia, schizoaffective disorder, delusional disorder, mental retardation or pervasive developmental disorder
  • suicidal or danger to others

结局指标

主要结局

Response rate at Day 21

次要结局

  • Change from baseline to Day 21 in other efficacy measures and safety

研究者

申办方类型
Industry

研究点 (21)

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