Major Depressive Disorder (MDD) With Mixed Features - Flexible Dose



Status:Completed
Conditions:Depression, Major Depression Disorder (MDD)
Therapuetic Areas:Psychiatry / Psychology, Pulmonary / Respiratory Diseases
Healthy:No
Age Range:18 - 75
Updated:4/21/2016
Start Date:September 2011
End Date:October 2014

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A Randomized, 6-Week, Double-Blind, Placebo-Controlled, Flexible-Dose, Parallel-Group Study of Lurasidone for the Treatment of Major Depressive Disorder With Mixed Features

Lurasidone HCl is a compound that is a candidate for the treatment of major depressive with
mixed features.This clinical study is designed to test how well Lurasidone works to treat
major depressive disorder with mixed features.


Inclusion Criteria:

- Subject provides written informed consent and is willing and able to comply with the
protocol in the opinion of the Investigator.

- Subject is 18 to 75 years of age, inclusive.

- Subject has MDD (diagnosed by DSM-IV-TR, and confirmed by the Structured - Clinical
Interview for DSM-IV Disorders - Clinical Trial version [SCID-CT]).

- Subject is currently experiencing a major depressive episode (diagnosed by DSM IV TR;
at least 2 weeks in duration) AND two or three of the following manic symptoms
occurring on most days over at least the last 2 weeks (confirmed by the SCID-CT
modified for Study D1050304):

- Elevated, expansive mood

- Inflated self-esteem or grandiosity

- More talkative than usual or pressure to keep talking

- Flight of ideas or subjective experience that thoughts are racing

- Increase in energy or goal-directed activity (either socially, at work or
school, or sexually)

- Increased or excessive involvement in activities that have a high potential for
painful consequences (e.g., engaging in unrestrained buying sprees, sexual
indiscretions, or foolish business investments)

- Decreased need for sleep (feeling rested despite sleeping less than usual; to be
contrasted from insomnia)

Exclusion Criteria:

- Subject has Axis I or Axis II diagnosis other than MDD that has been the primary
focus of treatment within the 3 months prior to screening.

- Subject answers "yes" to "Suicidal Ideation" Item 4 or 5 on the C-SSRS (at time of
evaluation) at screening or baseline visit.

- Subject has attempted suicide within the past 3 months.

- Subject has a lifetime history of any bipolar I manic or mixed manic episode.

- Subject has any abnormal laboratory parameter at screening that indicates a
clinically significant medical condition as determined by the Investigator.
We found this trial at
20
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Staten Island, New York 10305
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Birmingham, AL
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Boston, MA
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Brooklyn, NY
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Dallas, TX
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Dallas, Texas 75231
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Dallas, TX
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Dayton, OH
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Durham, North Carolina 27705
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Durham, NC
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Escondido, California 92025
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Escondido, CA
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Garden Grove, California 92845
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Garden Grove, CA
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New York, New York 10003
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New York, NY
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Palo Alto, California 94304
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Philadelphia, Pennsylvania 19139
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Philadelphia, PA
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Riverside, California 92506
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Riverside, CA
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Rochester, New York 14618
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Rochester, NY
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San Diego, California 92123
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San Diego, CA
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Sarasota, Florida 34201
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Sarasota, FL
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St. Charles, MO
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Wichita Falls, Texas 76309
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Wichita Falls, TX
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