Treatment of Patients With Major Depressive Disorder With MK0869 (0869-059)
NCT ID: NCT00035009
Last Updated: 2017-04-18
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
PHASE3
468 participants
INTERVENTIONAL
2001-09-20
2004-03-24
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
DOUBLE
Interventions
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MK0869, aprepitant
Comparator: paroxetine HCL
Eligibility Criteria
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Inclusion Criteria
18 Years
ALL
No
Sponsors
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Merck Sharp & Dohme LLC
INDUSTRY
Responsible Party
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Principal Investigators
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Medical Monitor
Role: STUDY_DIRECTOR
Merck Sharp & Dohme LLC
References
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Liu KS, Snavely DB, Ball WA, Lines CR, Reines SA, Potter WZ. Is bigger better for depression trials? J Psychiatr Res. 2008 Jul;42(8):622-30. doi: 10.1016/j.jpsychires.2007.07.003. Epub 2007 Sep 7.
Keller M, Montgomery S, Ball W, Morrison M, Snavely D, Liu G, Hargreaves R, Hietala J, Lines C, Beebe K, Reines S. Lack of efficacy of the substance p (neurokinin1 receptor) antagonist aprepitant in the treatment of major depressive disorder. Biol Psychiatry. 2006 Feb 1;59(3):216-23. doi: 10.1016/j.biopsych.2005.07.013. Epub 2005 Oct 24.
Study Documents
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Document Type: CSR Synopsis Links
View DocumentOther Identifiers
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Formally-1A407
Identifier Type: -
Identifier Source: secondary_id
MK0869-059
Identifier Type: -
Identifier Source: secondary_id
2006_402
Identifier Type: -
Identifier Source: secondary_id
0869-059
Identifier Type: -
Identifier Source: org_study_id
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