Major Depressive Disorder Clinical Trial
Official title:
Randomized, Double Blind, Placebo Controlled, Single IV Dose Parallel Efficacy and Safety Study of GLYX-13 in Subjects With Inadequate/Partial Response to Antidepressants During the Current Episode of Major Depressive Disorder
Verified date | September 2012 |
Source | Naurex, Inc |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The purpose of this study is to determine whether GLYX-13 reduces depression score in patients with treatment-resistant depression.
Status | Completed |
Enrollment | 115 |
Est. completion date | July 2012 |
Est. primary completion date | June 2012 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 65 Years |
Eligibility |
Inclusion Criteria: - diagnosis of major depressive disorder consistent with DSM-IV-TR - current episode greater than 8 weeks in duration - Hamilton Depression score >/- 21 - less than 25% reduction in depression during current episode assessed by ATRQ Exclusion Criteria: - Axis diagnosis of other psychiatric disorders - Experiencing hallucinations, delusions, other psychotic symptomatology - ECT during current episode |
Country | Name | City | State |
---|---|---|---|
United States | Mulitple | Evanston | Illinois |
Lead Sponsor | Collaborator |
---|---|
Naurex, Inc |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in depression score | 14 days | ||
Secondary | Change in BPRS+ | 14 days |
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