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Completed Phase 3 Interventional Results available

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

ClinicalTrials.gov ID: NCT00731120

Public ClinicalTrials.gov record NCT00731120. 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 10, 2026, 9:58 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, Fixed-Dose Study Comparing the Efficacy and Safety of 2 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 evaluate the safety and efficacy of 2.5 mg and 10 mg vortioxetine, once daily (QD), in adults with generalized anxiety disorder.

Study identification

NCT ID
NCT00731120
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Takeda
Industry
Enrollment
457 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
Jan 31, 2009
Last update posted
Dec 17, 2013

2008 – 2009

United States locations

U.S. sites
40
U.S. states
21
U.S. cities
40
Facility City State ZIP Site status
Not listed Birmingham Alabama
Not listed Anaheim California
Not listed Cerritos California
Not listed Costa Mesa California
Not listed Orange California
Not listed Redlands California
Not listed Cromwell Connecticut
Not listed Norwich Connecticut
Not listed Hockessin Delaware
Not listed Fort Myers Florida
Not listed Jacksonville Florida
Not listed Lady Lake Florida
Not listed Miami Florida
Not listed Atlanta Georgia
Not listed Chicago Illinois
Not listed Libertyville Illinois
Not listed Valparaiso Indiana
Not listed Overland Park Kansas
Not listed Prairie Village Kansas
Not listed Boston Massachusetts
Not listed Braintree Massachusetts
Not listed Pittsfield Massachusetts
Not listed St Louis Missouri
Not listed Cherry Hill New Jersey
Not listed Fresh Meadows New York
Not listed New York New York
Not listed Olean New York
Not listed Cincinnati Ohio
Not listed Columbus Ohio
Not listed Middleburg Heights Ohio
Not listed Oklahoma City Oklahoma
Not listed Emmaus Pennsylvania
Not listed Philadelphia Pennsylvania
Not listed Reading Pennsylvania
Not listed North Charleston South Carolina
Not listed Nashville Tennessee
Not listed Houston Texas
Not listed San Antonio Texas
Not listed Midlothian Virginia
Not listed Waukesha 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 NCT00731120, 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 10, 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 NCT00731120 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →