Glaucoma, Angle-closure, Primary, Acute Clinical Trial
Official title:
Phase IIA Double-Masked Randomized Sham-Controlled Trial of QPI-1007 Delivered by a Single Intravitreal Injection to Subjects With Acute Primary Angle-Closure Glaucoma (APACG)
This study will assess any side effects that may occur when QPI-1007 is injected into the eye in subjects with acute primary angle-closure glaucoma, as well as how long it takes for the body to clear the drug. This study will also test whether QPI-1007, injected into the eye, helps prevent both structural damage of the nerve tissue in the eye and the loss of visual function in subjects with acute primary angle-closure glaucoma.
This is a Phase IIa double-masked, single dose, randomized, sham-controlled study evaluating
the safety and tolerability, and pharmacokinetics of QPI-1007 versus Control (sham
procedure) in subjects with an acute attack of primary angle-closure glaucoma.
Subjects will be randomized at a ratio of 1:1 into one of two study arms: 1.5 QPI-1007 arm
or Control arm (sham procedure). The study will enroll approximately 30 subjects into each
arm. Randomization will be stratified by time from symptom onset to the study drug
administration or sham procedure (≤72 hours and >72 hours).
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Status | Clinical Trial | Phase | |
---|---|---|---|
Recruiting |
NCT01936129 -
Investigating the Neuroprotective Effect of Cop-1 (Copaxone) in Acute Primary Angle Closure
|
Phase 3 |