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Status:

COMPLETED

Safety and Effectiveness Study of BCI-540 Versus Placebo in the Treatment of Major Depressive Disorder With Concomitant Anxiety

Lead Sponsor:

BrainCells Inc.

Conditions:

Major Depressive Disorder

Anxiety

Eligibility:

All Genders

21-60 years

Phase:

PHASE2

Brief Summary

The purpose of this study is to determine whether BCI-540 80 mg given once daily (q.d.) or three times daily (t.i.d.) is effective in the treatment of major depression with concomitant anxiety.

Detailed Description

BCI-540 has been shown to be neurogenic in the Sponsor's in vitro neural stem cell analyses and in vivo animal models of depression and anxiety. These observations and the recent findings linking hipp...

Eligibility Criteria

Inclusion

  • The patient meets the DSM IV-TR criteria for Major Depressive Disorder (MDD) as determined by the Mini-International Neuropsychiatric Interview (MINI) and psychiatric evaluation.
  • The patient has a score of 20 or more on the HAM D17 scale, a score of 30 or more on the IDS-C30 and a score of 15 or more on the HAM-A scale at the Screening and Baseline visits.
  • The patient has a score of at least 2 on items 1 and 2 of the HAM-A scale at the Screening and Baseline visits.
  • The patient has a Clinical Global Impression of Severity (CGI S) rating of 4 or higher at the Screening and Baseline visits.
  • The patient has recurrent MDD.
  • The patient did not respond to at least one but no more than five adequate antidepressant trials during the current MDD episode.
  • The patient is living with another adult or has daily contact with an adult and contact information for the patient and this adult is available to the investigator.
  • Female patients of childbearing potential must be using a reliable, medically acceptable form of contraception for at least 30 days prior to the screening visit and must agree to continue such use throughout the duration of the study and for 30 days after the final dose of study drug.

Exclusion

  • The patient has a decrease of 20% or more in HAM D17 total score or HAM-A total score from the screening visit to the Baseline visit.
  • The patient represents significant risk of suicide in the opinion of the investigator at the screening or Baseline visit.
  • The patient has any other psychiatric Axis-I disorder (except GAD) as a principal diagnosis within 6 months of Screening.
  • The patient has a history of obsessive compulsive disorder, psychotic disorder, bipolar disorder, mental retardation.
  • The patient has a history of alcohol or substance (excluding nicotine or caffeine) abuse within 3 months of the screening visit, alcohol or substance dependence within 6 months of Screening.
  • The patient shows current evidence of substance abuse confirmed by results of a urine drug screen.
  • The patient has used an antidepressant medication (SSRI/SNRI or any other antidepressant medication, including MAOIs), within 1 week of Baseline(fluoxetine within 5 weeks).
  • The patient has a history of low RBC count, low hemoglobin, low WBC count, low platelets, or low reticulocyte counts of any aetiology other than that known to be related to blood loss, iron deficiency, or pregnancy.
  • The patient shows current evidence of macrocytosis, low RBC count, low haemoglobin, low WBC count, or low platelet count of any aetiology.
  • The patient will use drugs during the study (including follow-up) that are known to be related to agranulocytosis and/or aplastic anaemia.
  • The patient will receive interpersonal therapy and/or short-term (brief) dynamic therapy during the study.
  • The patient received ECT within 3 months of Screening.
  • The patient received depot antipsychotic therapy at any time.
  • The patient has used any antipsychotic or anxiolytic medications within 1 week of Screening.
  • The patient has used any drugs with known psychotropic properties or any non-psychotropic drugs with potential CNS effects within one week or 5-half lives (whichever is longer) of Screening.
  • The patient has a clinically significant cardiovascular, endocrine, hepatic, renal, pulmonary, gastrointestinal, neurological, malignancy, metabolic, psychiatric or other condition that might be detrimental to the patient if he or she participates in the study.
  • The patient has a known hypersensitivity to any cholinesterase inhibitors or cholinergic agonist drugs.
  • The patient is a pregnant or lactating woman.
  • The patient has a history of seizures.
  • The patient has clinically significant abnormalities on screening physical examination, ECG, serum chemistry, urinalysis tests, including thyroid stimulating hormone levels, as judged by the investigator.
  • The patient has a known positivity for human immunodeficiency virus, hepatitis B surface-antigen, or hepatitis C virus antibody.

Key Trial Info

Start Date :

January 1 2008

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

October 1 2009

Estimated Enrollment :

115 Patients enrolled

Trial Details

Trial ID

NCT00621270

Start Date

January 1 2008

End Date

October 1 2009

Last Update

October 24 2011

Active Locations (16)

Enter a location and click search to find clinical trials sorted by distance.

Page 1 of 4 (16 locations)

1

Grey Nuns Hospital, Clinical Research

Edmonton, Alberta, Canada, T6L 5X8

2

Okanagan Clinical Trials

Kelowna, British Columbia, Canada, V1Y 2H4

3

Dr. Alexander McIntyre, Inc

Penticton, British Columbia, Canada, V2A 4M4

4

University of British Columbia Mood Disorders Centre

Vancouver, British Columbia, Canada, V6T 2A1