Title

SA4503 8-Week Study in Major Depressive Disorder (MDD)
A Phase II, Multi-Centre, Randomized, Double-Blind, Placebo-Controlled, Parallel Group Study to Determine the Safety and Efficacy of Treatment With SA4503, Once Daily for 8 Weeks, in Subjects With Major Depressive Disorder
  • Phase

    Phase 2
  • Study Type

    Interventional
  • Status

    Completed No Results Posted
  • Intervention/Treatment

    cutamesine ...
  • Study Participants

    150
The purpose of this study is to determine the efficacy of SA4503 compared to placebo in the treatment of subjects with major depressive disorder (MDD). Secondary, to evaluate the safety of SA4503 compared to placebo in subjects with MDD.
Further study details as provided by M's Science Corporation:
Study Started
Nov 30
2007
Study Completion
Sep 30
2008
Last Update
Dec 18
2008
Estimate

Drug placebo

placebo, oral administration, once daily for 8 weeks

Drug SA4503 Low

Low dose, oral administration, once daily for 8 weeks

Drug SA4503 High

High dose, oral administration, once daily for 8 weeks

P Placebo Comparator

Placebo

A1 Experimental

SA4503

A2 Experimental

SA4503

Criteria

Inclusion Criteria:

Male or female between the ages of 18 and 65 (inclusive)
Diagnosis of MDD according to the Diagnostic and Statistical Manual of Mental Disorders (DSM)-IV criteria and a shortened MINI evaluation
HAM-D17 score of >/= 21 and a severity score of at least 2 for Item 1 (depressed mood) at both Screening and Baseline
Current depressive episode of at least 3 months duration, and significant depressed mood and anhedonia in the 4 weeks prior to Screening.

Exclusion Criteria:

Subjects who have received fluoxetine within 1 month prior to Baseline or any other antidepressant within 2 weeks prior to Baseline, or any unlicensed medication within 1 month before Screening
Subjects who require psychotropic medication other than the study medication
Subjects who started psychotherapy within 4 months prior to Screening
Subjects who currently (i.e., in the month prior to Screening) meet DSM-IV criteria for bipolar syndrome or psychotic depression or severe somatoform or eating disorders
Subjects who have a primary diagnosis of anxiety
Subjects who regularly use sleeping medication more than 3 times per week
Subjects who have major psychiatric or neurologic disorders other than MDD
Subjects with depression secondary to stroke, cancer, or other severe medical illness
Subjects who have a history of alcohol or substance dependence(within 1 year prior to Screening)
No Results Posted