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Completed

NCT Number: NCT00374920

Safety and Efficacy of MEM 1003 Versus Placebo for the Treatment of Patients With Bipolar I Disorder

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.

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Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Little Rock, Arkansas, United States

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About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 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

Exclusion criteria

  • 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

Treatment and study plan

MEM 1003

Drug

Primary outcomes

  1. Response rate at Day 21

Secondary outcomes

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

Sponsors and collaborators

Lead sponsor

Memory Pharmaceuticals

Industry

Collaborators

  • Stanley Medical Research Institute

Registry information

Official study title

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

Important dates

Study start
2006
Primary completion
2006
Study completion
2007
First posted
Sep 12, 2006
Registry last updated
May 6, 2008

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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