The objective of this study is to evaluate the safety and efficacy of LX211 as therapy in subjects with active non-infectious anterior uveitis
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
108
anterior chamber cells
Time frame: 16 and 24 weeks
BCVA
Time frame: 24 weeks
macular thickness
Time frame: 16 and 24 weeks
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0.6 mg/kg, twice a day (BID)
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
...and 20 more locations