Status:
COMPLETED
Efficacy, Safety and Tolerability of CX157 in Treatment Resistant Depression
Lead Sponsor:
CeNeRx BioPharma Inc.
Conditions:
Treatment Resistant Depression
Eligibility:
All Genders
20-65 years
Phase:
PHASE2
Brief Summary
The purpose of this study is to determine if CX157 is effective and safe in patients with treatment of treatment resistant depression over six weeks of treatment.
Detailed Description
The primary objective of this study is to examine the efficacy of CX157 Modified Release Tablet, 125 mg administered twice per day (BID) as compared to placebo in subjects with Treatment Resistant Dep...
Eligibility Criteria
Inclusion
- Male or female, 20 to 65 years of age
- Able to read, understand and converse in English and provide written, dated informed consent
- Diagnosed with Major Depressive Disorder (MDD)and Treatment Resistant Depression(TRD)
- Females on acceptable method of contraception
Exclusion
- Major depressive episode greater than five years
- A history of a Substance Use Disorder with the exception of nicotine dependence in the past 12 months
- Obsessive-Compulsive Disorder (OCD), Panic Disorder, Post-traumatic Stress Disorder (PTSD
- A history of schizophrenia or schizoaffective disorders
- A history of anorexia nervosa, bulimia nervosa, or eating disorder not otherwise specified, within the past five years
- A history of Antisocial Personality Disorder or Borderline Personality Disorder
- Recent suicidal behavior and is at risk of such behavior during the course of the study
- Electroconvulsive therapy (ECT) within the past five years
- Transcranial Magnetic Stimulation (TMS) for the treatment of the current episode of depression
- Vagus Nerve Stimulation (VNS) at any time
- Any psychoactive drugs within one to four weeks prior to the randomization visit depending on the type of drug
- Significant abnormality on the screening physical examination
- Significant cardiac abnormalities such as uncontrolled hypertension, recent myocardial infarction, Congestive heart failure (CHF), Angina pectoris
- A history within the past two years of significant head trauma, surgical procedure involving the brain,degenerative central nervous system disorder (e.g., Alzheimer's or Parkinson's Disease), epilepsy, mental retardation
- A history of hypothyroidism and has been on a stable dosage of thyroid replacement medication for less than six months
- A history of hyperthyroidism which was treated (medically or surgically) less than six months prior to screening
- Participation in an investigational study in the past one month
- A positive screening urine test for drugs of abuse
- Female subject who is pregnant or lactating
Key Trial Info
Start Date :
November 1 2010
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
May 1 2012
Estimated Enrollment :
360 Patients enrolled
Trial Details
Trial ID
NCT01246908
Start Date
November 1 2010
End Date
May 1 2012
Last Update
July 10 2012
Active Locations (30)
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1
Synergy Escondido
Escondido, California, United States, 92025
2
Synergy Clinical Research Center
National City, California, United States, 91950
3
Excell Research
Oceanside, California, United States, 92056
4
Pacific Clinical Research
Orange, California, United States, 92868