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A Double-Blind, Multicenter, Placebo and Active-Controlled, Acute Extension Study of 2 Doses of MK-0869 in the Treatment of Patients With Major Depressive Disorder
A clinical study to determine the efficacy and safety of MK0869 in the treatment of depression
The duration of treatment is 8 weeks.
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
Start Date
July 30, 2002
Primary Completion Date
December 31, 2003
Completion Date
December 31, 2003
Last Updated
May 5, 2017
600
ACTUAL participants
aprepitant
DRUG
Comparator: paroxetine HCL
DRUG
Comparator: Placebo (Unspecified)
DRUG
Lead Sponsor
Merck Sharp & Dohme LLC
NCT07115329
NCT06793397
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT07025720