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Treatment of Patients with Major Depressive Disorder with an Investigational Compound



Treatment of Patients with Major Depressive Disorder with an Investigational Compound

For Condition: Major Depressive Disorder
Status: No longer recruiting
Sponsor(s): Sponsor Name Pending ,
Synopsis: A clinical study to determine the efficacy and safety of an investigational medication in the treatment of depression
Details:
Eligibility:
Study Type:
  Interventional, Treatment, Safety/Efficacy Study
Minimum Age/Maximum Age: 18 Years/
Genders: Both
Protocol Entry Criteria: Patients with Major Depressive Disorder
Total Enrollment: 

Location and Contact Information:

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New Baltimore,  Michigan, 
United States
 

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Moorestown,  New Jersey, 
United States
 

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Atlanta,  Georgia, 
United States
 

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Washington D.C.,  District of Columbia, 
United States
 

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Charlottesville,  Virginia, 
United States
 


Additional Information:
Study ID Numbers:
  65MBS4W; 
Study Start Date: 
Record last reviewed: May 2004
Additional information available at: clinicaltrials.gov
Clinicaltrials.gov Reference link: NCT00048607

Other Major Depressive Disorder Studies:
1. Treatment of Patients with Major Depressive Disorder with an Investigational Compound

2. Treatment for Adolescents With Depression Study (TADS)

3. Pharmacologic Treatment of PTSD in Sexually Abused Children

4. Therapy for Depression with Co-occurring Panic or Anxiety Symptoms

5. Efficacy And Safety Of Two Fixed Doses Of DVS-233 SR In Adult Outpatients With Major Depressive Disorder

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Treatment of Patients with Major Depressive Disorder with an Investigational Compound

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