MRCT Evaluating NCX 470 vs. Latanoprost in Subjects With Open-Angle Glaucoma or Ocular Hypertension

Completed · Phase 3

Conditions studied: Open Angle Glaucoma, Ocular Hypertension

In brief

The objective of this clinical study is to evaluate the safety and efficacy of NCX 470 Ophthalmic Solution in lowering intraocular pressure (IOP) in subjecs with ocular hypertension or open-angle glaucoma. Subjects will be randomized in a 1:1 ratio to NCX 470 0.1% or to latanoprost 0.005% to be administered to both eyes once daily in the evening for up to 12 months.

Key facts

Study ID
NCT04630808
Run by
Nicox Ophthalmics, Inc.
People needed
696
Starts
2020-11-09
Expected to finish
2025-06-25
Last updated by the study team
2025-09-08

Who can join

Age: 18 and older, up to 84. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

You may not qualify if…

Where it is running

Full record on ClinicalTrials.gov

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