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Clinical Trial Summary

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.


Clinical Trial Description

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). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT01965106
Study type Interventional
Source Quark Pharmaceuticals
Contact
Status Completed
Phase Phase 2
Start date December 2013
Completion date July 2015

See also
  Status Clinical Trial Phase
Recruiting NCT01936129 - Investigating the Neuroprotective Effect of Cop-1 (Copaxone) in Acute Primary Angle Closure Phase 3