Clinical Trials Directory

Trials / Terminated

TerminatedNCT01111552

Study to Evaluate the Efficacy, Safety and Tolerability of an Oral Aripiprazole/Escitalopram Combination Therapy in Participants With Major Depressive Disorder (MDD)

A Multicenter, Randomized, Double-blind Study to Evaluate the Efficacy, Safety and Tolerability of an Oral Aripiprazole/Escitalopram Combination Therapy in Patients With Major Depressive Disorder

Status
Terminated
Phase
Phase 3
Study type
Interventional
Enrollment
237 (actual)
Sponsor
Otsuka Pharmaceutical Development & Commercialization, Inc. · Industry
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

Summary

This will be a multicenter, randomized, double-blind study designed to assess the efficacy, safety and tolerability of an oral Aripiprazole/Escitalopram combination therapy in participants with MDD who have demonstrated an incomplete response to a prospective trial of Escitalopram, and report a treatment history for the current MDD episode of an inadequate response to at least one and no more than three adequate trials of an approved antidepressant other than Escitalopram. An inadequate response is defined as less than a 50% reduction in depressive symptom severity as assessed by the participant's self-report on the Massachusetts General Hospital Antidepressant Treatment Response Questionnaire (ATRQ) and evaluated by the investigator as part of the participant's medical and psychiatric history. An adequate trial is defined as an antidepressant treatment for at least 6 weeks duration (or at least 3 weeks for combination treatments) at an approved dose as specified in the ATRQ.

Detailed description

The study will be organized as follows: * Screening Phase * Single-blind Prospective Treatment Phase * Single-blind Continuation Phase (Responder) or Double-blind Randomization Phase (non-Responder) * 30 day Post Treatment Follow-up Assigned Interventions: * Escitalopram monotherapy * Aripiprazole/Escitalopram combination therapy * Aripiprazole monotherapy

Conditions

Interventions

TypeNameDescription
DRUGEscitalopramEscitalopram oral capsules.
DRUGAripiprazoleAripiprazole oral capsules.
DRUGPlaceboStudy drug matching placebo capsule.

Timeline

Start date
2010-07-29
Primary completion
2011-09-27
Completion
2011-09-27
First posted
2010-04-27
Last updated
2021-10-26
Results posted
2021-10-26

Locations

60 sites across 7 countries: United States, Australia, Bulgaria, India, Philippines, Romania, Slovakia

Regulatory

Source: ClinicalTrials.gov record NCT01111552. Inclusion in this directory is not an endorsement.