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

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.