The objective of this study is to assess the efficacy and safety of gevokizumab in treating Behcet's disease uveitis (BDU).
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
4
Solution for subcutaneous injection
Solution for subcutaneous injection
Unnamed facility
Santa Ana, California, United States
Unnamed facility
Chicago, Illinois, United States
Unnamed facility
Ellsworth, Maine, United States
Unnamed facility
Cambridge, Massachusetts, United States
Time to first ocular exacerbation
Time to first ocular exacerbation is defined as the number of days from randomization to the first ocular exacerbation.
Time frame: Randomization through Day 280
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Unnamed facility
Royal Oak, Michigan, United States
Unnamed facility
Winston-Salem, North Carolina, United States
Unnamed facility
Fargo, North Dakota, United States
Unnamed facility
Houston, Texas, United States