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Completed Phase 3 Interventional

A Study of LX211 in Clinically Quiescent Non-infectious Intermediate, Anterior and Intermediate, Posterior or Pan-Uveitis

ClinicalTrials.gov ID: NCT00404742

Public ClinicalTrials.gov record NCT00404742. 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 Jul 22, 2026, 5:48 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 Double-Masked, Placebo-Controlled, Multi-Center, Parallel-Group, Dose-Ranging Study With an Optional Extension to Assess the Efficacy and Safety of LX211 as Therapy in Subjects With Clinically Quiescent Sight Threatening, Non-infectious Intermediate, Anterior and Intermediate, Posterior or Pan-Uveitis

Study identification

NCT ID
NCT00404742
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Lux Biosciences, Inc.
Industry
Enrollment
232 participants

Conditions and interventions

Interventions

  • Placebo Drug
  • LX211 Drug

Drug

Eligibility (public fields only)

Age range
13 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
Dec 31, 2006
Primary completion
Oct 31, 2008
Completion
Apr 30, 2009
Last update posted
Jun 21, 2012

2007 – 2009

United States locations

U.S. sites
19
U.S. states
14
U.S. cities
19
Facility City State ZIP Site status
University of Alabama at Birmingham Birmingham Alabama
Retinal Consultants of Arizona Phoenix Arizona 85014
University of Illinois - Chicago Chicago Illinois 60612
Midwest Eye Institute Indianapolis Indiana 46280
Wilmer Eye Institute Baltimore Maryland
Massachusetts Eye and Ear Infirmary Boston Massachusetts
Massachusetts Eye Research and Surgery Institute Cambridge Massachusetts 02142
Associated Retinal Consultants, PC Grand Rapids Michigan 49546
Tauber Eye Center Kansas City Missouri 64111
UMDNJ-New Jersey Medical School, Ophthalmology Dept. Newark New Jersey 07103
New York Eye & Ear Hospital New York New York 10003
Duke University Eye Center, Erwin Road Durham North Carolina
Oregon Health Sciences University Portland Oregon 97201
Texas Retina Associates Arlington Texas 76012
Brian B. Berger, MD, P.A. Austin Texas 78705
Texas Retina Associates Dallas Texas 75231
Vitreoretinal Consultants Houston Texas 77030
Retina & Uveitis Consultants of Texas San Antonio Texas 78240
Viginia Eye Consultants Norfolk Virginia 23502

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 22 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00404742, 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 Jun 21, 2012 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00404742 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →