The purpose of this study is to assess the safety, tolerability, and efficacy of AEB071 as a therapy for uveitis. Vision improvement and reduction in the swelling of retina will be measured for the assessment of efficacy.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
13
University of Southern California Doheny Eye Institute
Los Angeles, California, United States
University of California
San Francisco, California, United States
Colorado Retina Associates
Safety and tolerability of AEB071
Time frame: Baseline/Day 1 to Week 8 (Day 56) (end of study)
Change in the degree of inflammation in the study eye
Time frame: Baseline/Day 1, Week 8 (Day 56)/end of study
Change in the visual acuity of the study eye
Time frame: Baseline/Day 1, Week 8 (Day 56)/end of study
Change in macular edema in the study eye
Time frame: Baseline/Day 1, Week 8 (Day 56)/end of study
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Denver, Colorado, United States
University of Miami Miller School of Medicine; Anne Bates Leach Eye Hosptial;Bascom Palmer Eye Institute
Miami, Florida, United States
University of South Florida, Eye Institute
Tampa, Florida, United States
Emory University
Atlanta, Georgia, United States
John Hopkins Hospital/Wilmer Eye Institute
Baltimore, Maryland, United States
MERSI
Cambridge, Massachusetts, United States
Mayo Clinic Department of Opthalmology
Rochester, Minnesota, United States
Cornea and Laser Eye Institute
Teaneck, New Jersey, United States
...and 3 more locations