Safety and Efficacy of MEM 1003 Versus Placebo for the Treatment of Patients With Bipolar I Disorder
Primary Purpose
Bipolar Disorder With Manic or Mixed Episodes
Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
MEM 1003
Sponsored by
About this trial
This is an interventional treatment trial for Bipolar Disorder With Manic or Mixed Episodes focused on measuring bipolar, mania, mixed
Eligibility Criteria
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
Sites / Locations
Outcomes
Primary Outcome Measures
Response rate at Day 21
Secondary Outcome Measures
Change from baseline to Day 21 in other efficacy measures and safety
Full Information
NCT ID
NCT00374920
First Posted
September 9, 2006
Last Updated
May 5, 2008
Sponsor
Memory Pharmaceuticals
Collaborators
Stanley Medical Research Institute
1. Study Identification
Unique Protocol Identification Number
NCT00374920
Brief Title
Safety and Efficacy of MEM 1003 Versus Placebo for the Treatment of Patients With Bipolar I Disorder
Official 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
Study Type
Interventional
2. Study Status
Record Verification Date
May 2008
Overall Recruitment Status
Completed
Study Start Date
September 2006 (undefined)
Primary Completion Date
December 2006 (Actual)
Study Completion Date
March 2007 (Actual)
3. Sponsor/Collaborators
Name of the Sponsor
Memory Pharmaceuticals
Collaborators
Stanley Medical Research Institute
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
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.
Detailed Description
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.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Bipolar Disorder With Manic or Mixed Episodes
Keywords
bipolar, mania, mixed
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
Double
Allocation
Randomized
Enrollment
60 (false)
8. Arms, Groups, and Interventions
Intervention Type
Drug
Intervention Name(s)
MEM 1003
Primary Outcome Measure Information:
Title
Response rate at Day 21
Secondary Outcome Measure Information:
Title
Change from baseline to Day 21 in other efficacy measures and safety
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Stephen R Murray, MD, PhD
Organizational Affiliation
Memory Pharmaceuticals Corp
Official's Role
Study Director
Facility Information:
City
Little Rock
State/Province
Arkansas
ZIP/Postal Code
72201
Country
United States
City
Garden Grove
State/Province
California
ZIP/Postal Code
92845
Country
United States
City
Riverside
State/Province
California
ZIP/Postal Code
92506
Country
United States
City
San Diego
State/Province
California
ZIP/Postal Code
92105
Country
United States
City
Torrance
State/Province
California
ZIP/Postal Code
90502
Country
United States
City
Bradenton
State/Province
Florida
ZIP/Postal Code
34208
Country
United States
City
Ft Lauderdale
State/Province
Florida
ZIP/Postal Code
33301
Country
United States
City
Lake Charles
State/Province
Louisiana
ZIP/Postal Code
70601
Country
United States
City
Shreveport
State/Province
Louisiana
ZIP/Postal Code
71101
Country
United States
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02114
Country
United States
City
Willingboro
State/Province
New Jersey
ZIP/Postal Code
08046
Country
United States
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19149
Country
United States
City
Austin
State/Province
Texas
ZIP/Postal Code
78729
Country
United States
City
Austin
State/Province
Texas
ZIP/Postal Code
78745
Country
United States
City
Austin
State/Province
Texas
ZIP/Postal Code
78756
Country
United States
City
Bellaire
State/Province
Texas
ZIP/Postal Code
77401
Country
United States
City
Dallas
State/Province
Texas
ZIP/Postal Code
75228
Country
United States
City
Houston
State/Province
Texas
ZIP/Postal Code
77008
Country
United States
City
Irving
State/Province
Texas
ZIP/Postal Code
75062
Country
United States
City
Kirkland
State/Province
Washington
ZIP/Postal Code
98033
Country
United States
City
Kirkland
State/Province
Washington
ZIP/Postal Code
98034
Country
United States
12. IPD Sharing Statement
Learn more about this trial
Safety and Efficacy of MEM 1003 Versus Placebo for the Treatment of Patients With Bipolar I Disorder
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