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

Completed · Phase 2 · Has a placebo group

Conditions studied: Major Depressive Disorder

In brief

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.

Key facts

Study ID

NCT00739908

Run by

CeNeRx BioPharma Inc.

People needed

285

Starts

2008-09-01

Expected to finish

2009-07-01

Last updated by the study team

2012-06-27

Who can join

Age: 18 and older, up to 60. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Male or female = 18 years of age and <60 years
• Able to read, understand, converse in English
• Willing to comply with diet restrictions, concomitant medication restrictions, \& all study requirements
• Good general health as ascertained by:Medical history, Physical exam, Supine \& standing vital signs, Clinical lab evaluations, 12-lead Electrocardiogram (ECG)
• Diagnosis of MDD;
• A total score =>40 on the IDS-SR30 assessed via IVRS at Screening and Randomization

You may not qualify if…

• Subject's current MDD episode is >2 years
• History of Substance Use Disorder at Screening or 12 months prior (except for nicotine)
• Current diagnosis of Obsessive-Compulsive Disorder;
• Panic Disorder or Post-Traumatic Stress Disorder;
• Anorexia nervosa, Bulimia nervosa, or eating disorder not otherwise specified;
• Any Axis I Disorder clinically predominant to their MDD (within 6 mo);
• Presence of psychotic features with current depressive episode;
• Antisocial or Borderline Personality Disorder
• At risk for suicide
• Lack of response to >2 trials of adequate dose \& duration of antidepressants of different mechanistic classes
• Electroconvulsive therapy within 1 year of Screening
• Subject has taken any psychoactive drug within 2 weeks of Randomization
• History of cardiac abnormalities including abnormal vital sign measurements
• Clinically significant abnormal ECG at Screening
• History within past 2 years of: Significant head trauma;
• Surgical procedure involving brain or meninges; Encephalitis or meningitis;
• Degenerative CNS disorder (Alzheimer's or Parkinson's);
• Epilepsy;
• Mental retardation
• Clinically significant Liver Function Test (LFT) and other lab abnormalities
• A history of hypothyroidism and treatment with a stable dosage of thyroid replacement medication for <6 months prior to Screening
• A history of hyperthyroidism treated (medically or surgically) <6 months prior to Screening
• Participation in a clinical investigation of a psychotropic drug within 90 days prior to Screening OR used any other investigational drug within 60 days prior to Screening
• Presence of any medical history which includes:
• Hypersensitivity to CX157 or excipients, other MAO inhibitors, or other phenylethylamines;

Where it is running

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

Full record on ClinicalTrials.gov

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