The purpose of this study was to assess the safety and efficacy of AL-59412C injected intravitreally relative to Vehicle.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Enrollment
4
Concentration 1 and Concentration 2
Inactive ingredients used as placebo
Maximum intraocular (IOP) reduction from baseline up to 24 hours post-injection
IOP was measured by Goldman applanation tonometry at protocol-specified timepoints, up to 24 hours post-injection.
Time frame: Time to event, up to 24 hours post-injection
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