Safety and Efficacy of EVT 101 in Treatment-Resistant Depression

• Status: Terminated
• Trial end date: 2011-03-01
• Target enrollment: 0
• Participant gender: All

Summary

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.

• Phase: Phase 2
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Janssen Research & Development, LLC
• Collaborator: Hoffmann-La Roche

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