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Completed Phase 3 Interventional Results available

Efficacy of Vortioxetine (Lu AA21004) in Treating Generalized Anxiety Disorder

ClinicalTrials.gov ID: NCT00730691

Public ClinicalTrials.gov record NCT00730691. 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 Sep 1, 2026, 6:01 PM 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 Randomized, Double-Blind, Parallel-Group, Placebo-Controlled, Active-Referenced, Fixed-Dose Study Comparing the Efficacy and Safety of 3 Doses of Lu AA21004 in Acute Treatment of Adults With Generalized Anxiety Disorder

Brief summary

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

The purpose of this study is to determine the safety and efficacy of vortioxetine, once daily (QD), in adults with generalized anxiety disorder.

Study identification

NCT ID
NCT00730691
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Takeda
Industry
Enrollment
781 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 65 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

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

Study timeline

Start date
May 31, 2008
Primary completion
Jan 31, 2009
Completion
Jan 31, 2009
Last update posted
Dec 17, 2013

2008 – 2009

United States locations

U.S. sites
66
U.S. states
28
U.S. cities
66
Facility City State ZIP Site status
Not listed Anaheim California
Not listed Beverly Hills California
Not listed Fresno California
Not listed Los Angeles California
Not listed Oceanside California
Not listed San Diego California
Not listed Sherman Oaks California
Not listed Widomar California
Not listed Denver Colorado
Not listed Farmington Connecticut
Not listed Norwalk Connecticut
Not listed Coral Gables Florida
Not listed Jacksonville Florida
Not listed Maitland Florida
Not listed Miami Florida
Not listed Orlando Florida
Not listed Tampa Florida
Not listed West Palm Beach Florida
Not listed Winter Park Florida
Not listed Atlanta Georgia
Not listed Roswell Georgia
Not listed Smyrna Georgia
Not listed Honolulu Hawaii
Not listed Oakbrook Ter Illinois
Not listed Terre Haute Indiana
Not listed Owensboro Kentucky
Not listed Shreveport Louisiana
Not listed Rockville Maryland
Not listed Chesterfield Missouri
Not listed St Louis Missouri
Not listed Nashua New Hampshire
Not listed Clementon New Jersey
Not listed Princeton New Jersey
Not listed Albuquerque New Mexico
Not listed Brooklyn New York
Not listed Cedarhurst New York
Not listed New York New York
Not listed Rochester New York
Not listed Staten Island New York
Not listed Charlotte North Carolina
Not listed Raleigh North Carolina
Not listed Beachwood Ohio
Not listed Cleveland Ohio
Not listed Dayton Ohio
Not listed Toledo Ohio
Not listed Eugene Oregon
Not listed Portland Oregon
Not listed Salem Oregon
Not listed Allentown Pennsylvania
Not listed Media Pennsylvania
Not listed Philadelphia Pennsylvania
Not listed Columbia South Carolina
Not listed Memphis Tennessee
Not listed Nashville Tennessee
Not listed Dallas Texas
Not listed DeSoto Texas
Not listed Houston Texas
Not listed Lake Jackson Texas
Not listed Wichita Falls Texas
Not listed Midvale Utah
Not listed Woodstock Vermont
Not listed Richmond Virginia
Not listed Seattle Washington
Not listed Brown Deer Wisconsin
Not listed Middleton Wisconsin
Not listed Milwaukee Wisconsin

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 NCT00730691, 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 Dec 17, 2013 · Synced Sep 1, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00730691 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →