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The primary purpose of this study is to evaluate the efficacy and safety of two doses of DVS SR (50 and 100 mg/day) in the treatment of adults with Major Depressive Disorder.
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Lead Sponsor
Pfizer
NCT07227454 · Depressive Disorder, Major
NCT05415397 · Depressive Disorder, Major, Inflammation
NCT07059234 · Depressive Disorder, Major
NCT06396312 · Depressive; Disorder, Major, Single Episode, Major, With Psychotic Symptoms, Depressive; Disorder, Major, Single Episode, Major (Without Psychotic Symptoms), and more
NCT06136546 · Depressive Disorder, Major, Inflammation
Pfizer Investigational Site
Beverly Hills, California
Pfizer Investigational Site
Burbank, California
Pfizer Investigational Site
Encino, California
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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.
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