Efficacy and Safety of Lu AA21004 in Treating Adult Subjects With Major Depressive Disorder

Inclusion Criteria:

• The subject suffers from a major depressive episode as the primary 1. Suffers from a major depressive episode as the primary diagnosis according to Diagnostic and Statistical Manual of Mental Disorders, 4th Edition, Text Revision (DSM-IV-TR) criteria.
• The reported duration of the current MDE is at least 3 months.
• Has a Montgomery Åsberg Depression Rating Scale total score greater than or equal to 30.
• Females of childbearing potential who are sexually active must agree to use adequate contraception, and can neither be pregnant nor lactating from Screening throughout the duration of the study.

Exclusion Criteria:

• Has received any investigational compound less than 30 days before Screening or 5 half-lives prior to Screening, whichever is longer.
• Has received Lu AA21004 in a previous clinical study.

• Has 1 or more the following:

  • Any current psychiatric disorder other than major depressive disorder as defined in the DSM-IV-TR (as assessed by the Mini International Neuropsychiatric Interview)
  • Current or past history of: manic or hypomanic episode, schizophrenia, or any other psychotic disorder, including major depression with psychotic features, mental retardation, organic mental disorders, or mental disorders due to a general medical condition as defined in the DSM-IV-TR.
  • Any substance disorder (except nicotine and caffeine) within the previous 6 months as defined in the DSM-IV-TR.
  • Presence or history of a clinically significant neurological disorder (including epilepsy).
  • Neurodegenerative disorder (Alzheimer disease, Parkinson disease, multiple sclerosis, Huntington disease, etc).
  • Any Axis II disorder that might compromise the study.

• Is required to take or intends to continue taking any disallowed medication, any prescription medication, herbal treatment or over-the counter medication that may interfere with evaluation of the study medication, including:

  • Narcotic analgesics
  • Nonsteroidal anti-inflammatory drugs
  • Rifampin
  • Macrolide antibiotics
  • Hormones (only thyroid hormone replacement, contraceptives [oral, patch], estrogen and progesterone replacement therapy are allowed in chronic use)
  • Hypoglycemic agents (chronic use is allowed)
  • Insulin (chronic use is allowed)
  • Systemic steroids
  • Quinidine
  • Antineoplastics
  • Antiobesity agents
• The subject has a significant risk of suicide according to the investigator's opinion or has a score greater than or equal to 5 on item 10 (suicidal thoughts) of the Montgomery Åsberg Depression Rating Scale or has made a suicide attempt in the previous 6 months.
• The current depressive symptoms of the subject are considered by the investigator to have been resistant to 2 adequate antidepressant treatments of at least 6 weeks duration each.
• The subject has received electroconvulsive therapy within 6 months prior to Screening.
• The subject is currently receiving formal cognitive or behavioral therapy, systematic psychotherapy, or plans to initiate such therapy during the study.
• The subject has a clinically significant unstable illness, for example, hepatic impairment or renal insufficiency, or a cardiovascular, pulmonary, gastrointestinal, endocrine, neurological, rheumatologic, immunologic, infectious, skin and subcutaneous tissue disorders, or metabolic disturbance.
• The subject has an alanine aminotransferase, aspartate aminotransferase or total bilirubin level greater than 1.5 times the upper limits of normal.
• The subject has a serum creatinine greater than 1.5 times the upper limits of normal.
• The subject has a previous history of cancer that had been in remission for less than 5 years prior to the first dose of study medication. This criterion does not include those subjects with basal cell or Stage I squamous cell carcinoma of the skin.
• The subject has clinically significant abnormal vital signs as determined by the investigator.
• The subject has an abnormal electrocardiogram determined by the central reader and confirmed as clinically significant by the investigator.
• The subject has 1 or more laboratory values outside the normal range, based on the blood or urine samples taken at the Screening Visit, that are considered by the investigator to be clinically significant.
• The subject has a thyroid stimulating hormone value outside the normal range at Screening Visit that is determined to be clinically significant by the investigator.
• The subject has a disease or takes medication that, in the opinion of the investigator, could interfere with the assessments of safety, tolerability, or efficacy.
• The subject has previously enrolled in this study.