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Completed Phase 2 Interventional

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

ClinicalTrials.gov ID: NCT00374920

Public ClinicalTrials.gov record NCT00374920. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 26, 2026, 5:45 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

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

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

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.

Study identification

NCT ID
NCT00374920
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Memory Pharmaceuticals
Industry
Enrollment
60 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 65 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Sep 2006 (Type not available)
Primary completion
Dec 2006 (Actual)
Completion
Mar 2007 (Actual)
Last update posted
May 6, 2008

2006 – 2007

United States locations

U.S. sites
21
U.S. states
9
U.S. cities
18
Facility City State ZIP Site status
Not listed Little Rock Arkansas 72201 —
Not listed Garden Grove California 92845 —
Not listed Riverside California 92506 —
Not listed San Diego California 92105 —
Not listed Torrance California 90502 —
Not listed Bradenton Florida 34208 —
Not listed Fort Lauderdale Florida 33301 —
Not listed Lake Charles Louisiana 70601 —
Not listed Shreveport Louisiana 71101 —
Not listed Boston Massachusetts 02114 —
Not listed Willingboro New Jersey 08046 —
Not listed Philadelphia Pennsylvania 19149 —
Not listed Austin Texas 78729 —
Not listed Austin Texas 78745 —
Not listed Austin Texas 78756 —
Not listed Bellaire Texas 77401 —
Not listed Dallas Texas 75228 —
Not listed Houston Texas 77008 —
Not listed Irving Texas 75062 —
Not listed Kirkland Washington 98033 —
Not listed Kirkland Washington 98034 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00374920, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted May 6, 2008 · Synced Oct 26, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00374920 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →