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

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
BrainCells Inc.
ClinicalTrials.gov Identifier:
NCT00621270
First received: February 11, 2008
Last updated: October 20, 2011
Last verified: October 2011

February 11, 2008
October 20, 2011
January 2008
October 2009   (final data collection date for primary outcome measure)
Co-primary outcome measures will be the change from Baseline to Week 6 on the total score of the Inventory of Depressive Symptomatology-Clinician Version (IDS-C30) and the Hamilton Rating Scale for Anxiety (HAM-A). [ Time Frame: Week 6 ] [ Designated as safety issue: No ]
Same as current
Complete list of historical versions of study NCT00621270 on ClinicalTrials.gov Archive Site
The safety, tolerability and side effect profile of BCI-540 will also be measured by adverse events, clinical laboratory values, electrocardiograms, vital signs, and the Physician Withdrawal Checklist (PWC). [ Time Frame: Weeks 2, 4, 6, 7 and 12 ] [ Designated as safety issue: Yes ]
Same as current
Not Provided
Not Provided
 
Safety and Effectiveness Study of BCI-540 Versus Placebo in the Treatment of Major Depressive Disorder With Concomitant Anxiety
A 6-Week Randomised Double-Blind, Placebo-Controlled Study of BCI-540 80 mg q.d. and 80 mg t.i.d. in the Treatment of Adults With Major Depressive Disorder and Concomitant Anxiety

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.

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 hippocampal function and neurogenesis to mood disorders support the evaluation of the efficacy, safety, and tolerability of BCI-540 in patients with major depressive disorder with concomitant anxiety.

Interventional
Phase 2
Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor)
Primary Purpose: Treatment
  • Major Depressive Disorder
  • Anxiety
Drug: BCI-540
BCI-540 80 mg once (q.d.) or three times (t.i.d.) a day versus placebo
  • Experimental: 1
    BCI-540 80 mg once a day (q.d.)
    Intervention: Drug: BCI-540
  • Experimental: 2
    BCI-540 80 mg three times a day (t.i.d.)
    Intervention: Drug: BCI-540
  • Placebo Comparator: 3
    Placebo
    Intervention: Drug: BCI-540
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
115
October 2009
October 2009   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • 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 Criteria:

  • 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.
Both
21 Years to 60 Years
No
Contact information is only displayed when the study is recruiting subjects
Canada
 
NCT00621270
BCI-540-CL-001
No
BrainCells Inc.
BrainCells Inc.
Not Provided
Study Chair: Allan H. Young, MB ChB, MPhil, PhD, FRCPsych Institute of Mental Health, Dept. of Psychiatry, University of British Columbia
BrainCells Inc.
October 2011

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP