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Completed Phase 3 Interventional Results available

An Efficacy and Safety Study of Vortioxetine (Lu AA21004) in Treating Generalized Anxiety Disorder

ClinicalTrials.gov ID: NCT00734071

Public ClinicalTrials.gov record NCT00734071. 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 2, 2026, 12:16 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 Randomized, Double-Blind, Parallel-Group, Placebo-Controlled, Fixed-Dose Study Comparing the Efficacy and Safety of Single Dose 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 treating Generalized Anxiety Disorder.

Study identification

NCT ID
NCT00734071
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Takeda
Industry
Enrollment
304 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years and older
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
Dec 31, 2008
Completion
Feb 28, 2009
Last update posted
Dec 17, 2013

2008 – 2009

United States locations

U.S. sites
33
U.S. states
18
U.S. cities
33
Facility City State ZIP Site status
Not listed Anaheim California
Not listed Arcadia California
Not listed Irvine California
Not listed National City California
Not listed Sherman Oaks California
Not listed Upland California
Not listed Washington D.C. District of Columbia
Not listed Bradenton Florida
Not listed Coral Gables Florida
Not listed North Miami Florida
Not listed St. Petersburg Florida
Not listed Tampa Florida
Not listed Oak Brook Illinois
Not listed Park Ridge Illinois
Not listed Lafayette Indiana
Not listed Wichita Kansas
Not listed Baltimore Maryland
Not listed Fall River Massachusetts
Not listed Worcester Massachusetts
Not listed Flowood Mississippi
Not listed Brooklyn New York
Not listed New York New York
Not listed The Bronx New York
Not listed Morganton North Carolina
Not listed Cincinnati Ohio
Not listed Toledo Ohio
Not listed Oklahoma City Oklahoma
Not listed Portland Oregon
Not listed Lincoln Rhode Island
Not listed Memphis Tennessee
Not listed Austin Texas
Not listed San Antonio Texas
Not listed Charleston West Virginia

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 NCT00734071, 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 2, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00734071 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →