Expired Study
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Baltimore, Maryland


Purpose:

This study is a 4-week, randomized, double-blind, parallel-group, placebo-controlled monotherapy study in patients with treatment-resistant major depression. After confirmation of treatment-resistance in a prospective treatment period with citalopram, each patient will be treated with either EVT 101 once daily or placebo for 28 consecutive days.


Criteria:

Inclusion Criteria: - Major Depressive Disorder - Current episode of major depression that has not benefited from at least 1 but no more than 3 adequate treatment regimens - Has as score of >/= 18 on the Ham-D-17 Exclusion Criteria: - Pregnant or breast-feeding women - Evidence of age-related cognitive decline or mild dementia - At imminent risk of committing suicide - Has with the exception of major depression, a serious medical or neurological illness, including seizure disorder, stroke, dementia, or Parkinson disease - Has an established diagnosis of bipolar disorder, hypomania, schizoaffective disorder, major depression with psychotic features or schizophrenia - Has had a substance or alcohol abuse or dependence disorder (except nicotine and caffeine) in the 1 year before screening


NCT ID:

NCT01128452


Primary Contact:

Study Director
Doris Greiling, PhD
Evotec AG


Backup Contact:

N/A


Location Contact:

Baltimore, Maryland
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: October 09, 2019

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