CompletedPhase 3NCT00404885
A Multi-center Study to Assess the Efficacy and Safety of LX211 in Active Non-infectious Anterior Uveitis
Studying Anterior uveitis
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Lux Biosciences, Inc.
- Principal Investigator
- Eddy Anglade, M.D., MDChief Medical Officer
- Intervention
- Placebo(drug)
- Enrollment
- 108 enrolled
- Eligibility
- 13 years · All sexes
- Timeline
- 2007 – 2009
Study locations (30)
- University of Alabama at Birmingham, Birmingham, Alabama, United States
- Retinal Consultants of Arizona, Phoenix, Arizona, United States
- University of Illinois - Chicago, Chicago, Illinois, United States
- Wilmer Eye Institute, Baltimore, Maryland, United States
- Massachusetts Eye and Ear Infirmary, Boston, Massachusetts, United States
- Massachusetts Eye Research and Surgery Institute, Cambridge, Massachusetts, United States
- Associated Retinal Consultants, PC, Grand Rapids, Michigan, United States
- Tauber Eye Center, Kansas City, Missouri, United States
- New York Eye & Ear Hospital, New York, New York, United States
- Duke University Eye Center, Erwin Road, Durham, North Carolina, United States
- Oregon Health Sciences University, Portland, Oregon, United States
- Brian B. Berger, MD, P.A., Austin, Texas, United States
- Retina & Uveitis Consultants of Texas, San Antonio, Texas, United States
- Viginia Eye Consultants, Norfolk, Virginia, United States
- Universitätsklinik für Augenheilkunde, Salzburg, Austria
- +15 more locations on ClinicalTrials.gov
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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