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Phase 3 Completed N=366 Randomized Quadruple-blind Treatment

Efficacy Study of Vortioxetine (Lu AA21004) for Treatment of Major Depressive Disorder

Source: ClinicalTrials.gov NCT01355081 ↗
Enrolled (actual)
366
Serious AEs
0.8%
Results posted
Nov 2014
Primary outcomePrimary: Change From Baseline in Montgomery-Åsberg Depression Rating Scale (MADRS) Total Score After 8 Weeks of Treatment — -15.84; -14.85; -13.81 scores on a scale — p=0.1031

Summary

The purpose of this study is to assess the efficacy, safety and tolerability of 8-week treatment with Vortioxetine (Lu AA21004), once daily (QD), in Japanese participants with major depressive disorder. The purpose of this study is to assess the efficacy, safety and tolerability of 8-week treatment with Lu AA21004, once daily (QD), in Japanese participants with major depressive disorder.

Outcome Measures

OutcomeResultp-value
PRIMARY
Change From Baseline in Montgomery-Åsberg Depression Rating Scale (MADRS) Total Score After 8 Weeks of Treatment
-15.84; -14.85; -13.81 0.1031
SECONDARY
Percentage of Patients With MADRS Response After 8 Weeks of Treatment
51.3; 45.9; 39.8
SECONDARY
Percentage of Patients With MADRS Remission After 8 Weeks of Treatment
29.4; 28.7; 22.0
SECONDARY
Change From Baseline in the Hamilton Depression Scale (HAM-D17) Total Score After 8 Weeks of Treatment
-9.56; -8.54; -8.40
SECONDARY
Clinical Global Impression Scale-Improvement (CGI-I) Score After 8 Weeks of Treatment
2.44; 2.57; 2.66
SECONDARY
Change From Baseline in Sheehan Disability Scale (SDS) Total Score After 8 Weeks of Treatment
-5.01; -4.02; -2.91

Eligibility Criteria

Inclusion Criteria

  • The subject suffers from Major Depressive Disorder (MDD) as the primary diagnosis according to the Diagnostic and Statistical Manual of Mental Disorders, 4th Edition, Text Revision (DSM-IV-TR) criteria (classification code 296.2x and 296.3x).
  • The reported duration of the current major depressive episode is at least 3 months at the Screening Visit.
  • The subject has a Montgomery-Åsberg Depression Rating Scale (MADRS) total score ≥26 at the Screening and Baseline Visits.
  • The subject has a Clinical Global Impression Scale-Severity (CGI-S) score ≥4 at the Screening and Baseline Visits

Exclusion Criteria

  • The subject has one or more of the following conditions:
  • Any current psychiatric disorder other than MDD as defined in the DSM-IV-TR. A subject who exhibits symptoms of anxiety is eligible unless the subject fulfills the diagnostic criteria for a current anxiety disorder per DSM-IV-TR.
  • Current diagnosis or 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.
  • Current diagnosis or history of any substance-related disorder (except nicotine and caffeine-related disorders) as defined in the DSM-IV-TR.
  • Presence or history of a clinically significant neurological disorder (including epilepsy).
  • Neurodegenerative disorder (Alzheimer's disease, Parkinson's disease, multiple sclerosis, Huntington's disease, etc.).
  • Any DSM-IV-TR axis II disorder that might compromise the study.
  • 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 is at significant risk of suicide or has a score ≥5 on Item 10 (suicidal thoughts) of the MADRS at the Screening and Baseline Visit, or has attempted suicide within 6 months prior to the Screening Visit.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01355081). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

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