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Rocklatan® Evaluation

Glaucoma Clinical Trial

Official title:
A Multicenter, Open-Label Rocklatan® (Netarsudil/Latanoprost Ophthalmic Solution) 0.02%/0.005% Evaluation of IOP Lowering Efficacy and Safety as Replacement of Current Medical Therapy Regimen for the Reduction of Elevated Intraocular Pressure in Patients With Glaucoma or Ocular Hypertension

Clinical Trial Summary

The objective of this study is to evaluate the IOP-lowering effect when subjects are switched from various latanoprost-based regimens to Rocklatan. Subjects will stop their IOP-lowering medical therapy regimen and dose with Rocklatan for the duration of the study (12 weeks).

Clinical Trial Description

Enrollment will be stratified according to subject's IOP-lowering medical therapy regimen as follows: - Latanoprost monotherapy (Latanoprost Mono) - Latanoprost plus 1 additional IOP-lowering agent (Latanoprost +1) - Latanoprost plus 2 additional IOP-lowering agents (Latanoprost +2) Aerie Pharmaceuticals was acquired by Alcon Research LLC on November 22, 2022. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05283395
Study type Interventional
Source Aerie Pharmaceuticals
Contact
Status Completed
Phase Phase 4
Start date March 28, 2022
Completion date March 22, 2023
View Details
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