24-hour Efficacy of AR-12286

Completed · Phase 2

Conditions studied: Open Angle Glaucoma, Ocular Hypertension

In brief

An open-label, non-comparative, pilot evaluation of the 24-hour ocular hypotensive efficacy of AR-12286 in patients with open-angle glaucoma or ocular hypertension

Key facts

Study ID
NCT01330979
Run by
Aerie Pharmaceuticals
People needed
5
Starts
2011-05-01
Expected to finish
2012-08-01
Last updated by the study team
2014-04-21

Who can join

Age: 40 and older, up to 80. Sex: any. Healthy volunteers: not accepted.

Where it is running

Full record on ClinicalTrials.gov

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