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
| Type | Name | Description |
|---|---|---|
| DRUG | Escitalopram | Escitalopram oral capsules. |
| DRUG | Aripiprazole | Aripiprazole oral capsules. |
| DRUG | Placebo | Study 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
- FDA-regulated drug study
Source: ClinicalTrials.gov record NCT01111552. Inclusion in this directory is not an endorsement.