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Completed Phase 2 Interventional Results available

A Study of CX157 (TriRima) for the Treatment of Depression

ClinicalTrials.gov ID: NCT00739908

Public ClinicalTrials.gov record NCT00739908. 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 Sep 10, 2026, 10:51 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 Randomized, Double-Blind, Placebo-Controlled Parallel-Group, Assessment of the Efficacy, Safety and Tolerability of CX157 (TriRima) 60mg Three Times a Day (TID) in Subjects With Major Depressive Disorder

Brief summary

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

The purpose of this study is to examine the efficacy of CX157 60 mg administered three times a day (180 mg daily dose) as compared to placebo in subjects with Major Depressive Disorder (MDD). Secondary objectives are to evaluate the safety and tolerability and steady state pharmacokinetic profile of CX157 in these subjects.

Study identification

NCT ID
NCT00739908
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
CeNeRx BioPharma Inc.
Industry
Enrollment
285 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years to 60 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
Aug 31, 2008
Primary completion
Jun 30, 2009
Completion
Jun 30, 2009
Last update posted
Jun 26, 2012

2008 – 2009

United States locations

U.S. sites
14
U.S. states
14
U.S. cities
14
Facility City State ZIP Site status
Birmingham Research Group Birmingham Alabama 35216
Southwestern Research, Inc. Beverly Hills California
The George Washington University Washington D.C. District of Columbia
Irving S. Kolin, M.D. Winter Park Florida 32789
Midwest Center for Neurobehavioral Medicine Oakbrook Terrace Illinois
Capital Clinical Research Associates Rockville Maryland
McLean Hospital Belmont Massachusetts
CRI Worldwide, LLC Clementon New Jersey
Fieve Clinical Services New York New York
Richard H. Weisler, M.D., P.A. Raleigh North Carolina
University of Pennsylvania School of Medicine Philadelphia Pennsylvania
FutureSearch Trials Austin Texas 78756
Summit Research Network (Seattle), LLC Seattle Washington
Northbrooke Research Center Brown Deer Wisconsin

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 NCT00739908, 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 Jun 26, 2012 · Synced Sep 10, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00739908 live on ClinicalTrials.gov.

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