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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Notify MeKey information
Conditions
Age range
18 year–65 year
Sex eligibility
All sexes
Study type
Interventional
Phase
Phase 2
Primary location
Little Rock, Arkansas, United States
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
Primary outcomes
-
Response rate at Day 21
Secondary outcomes
-
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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