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Completed Phase 3 Interventional Results available

Study Evaluating Desvenlafaxine Succinate Sustained Release (DVS SR) In The Treatment Of Major Depressive Disorder

ClinicalTrials.gov ID: NCT00384033

Public ClinicalTrials.gov record NCT00384033. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 18, 2026, 8:07 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Duloxetine-Referenced, Parallel-Group Study to Evaluate the Efficacy and Safety of 2 Fixed Doses (50mg, 100mg) of Desvenlafaxine Sustained-Release Tablets in Adult Outpatients With Major Depressive Disorder

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

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.

Study identification

NCT ID
NCT00384033
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Pfizer
Industry
Enrollment
638 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Not listed

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Sep 2006 (Type not available)
Primary completion
Sep 2007 (Actual)
Completion
Sep 2007 (Actual)
Last update posted
Mar 15, 2012

2006 – 2007

United States locations

U.S. sites
22
U.S. states
11
U.S. cities
22
Facility City State ZIP Site status
Pfizer Investigational Site Beverly Hills California 90210 —
Pfizer Investigational Site Burbank California 91506 —
Pfizer Investigational Site Encino California 91316 —
Pfizer Investigational Site Los Alamitos California 90720 —
Pfizer Investigational Site Newport Beach California 92660 —
Pfizer Investigational Site Northridge California 91324 —
Pfizer Investigational Site Orange California 92868 —
Pfizer Investigational Site Pasadena California 91105 —
Pfizer Investigational Site Upland California 91786 —
Pfizer Investigational Site South Miami Florida 33143 —
Pfizer Investigational Site St. Petersburg Florida 33702 —
Pfizer Investigational Site Edwardsville Illinois 62025 —
Pfizer Investigational Site Farmington Hills Michigan 48336 —
Pfizer Investigational Site Flint Michigan 48507 —
Pfizer Investigational Site Okemos Michigan 48864 —
Pfizer Investigational Site Clementon New Jersey 08021 —
Pfizer Investigational Site Dayton Ohio 45408 —
Pfizer Investigational Site Portland Oregon 97210 —
Pfizer Investigational Site Philadelphia Pennsylvania 19149 —
Pfizer Investigational Site Salt Lake City Utah 84107 —
Pfizer Investigational Site Seattle Washington 98104 —
Pfizer Investigational Site Brown Deer Wisconsin 53223 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00384033, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Mar 15, 2012 · Synced Oct 18, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00384033 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →