Next Generation Rocklatan

Status Not yet recruiting

Clinical Trial Summary

The purpose of this two-stage clinical trial is to assess the safety and hypotensive efficacy of AR-17043 and PG043 ophthalmic solutions in subjects with open-angle glaucoma (OAG) or ocular hypertension (OHT).

Clinical Trial Description

During Stage 1, approximately 100 adult subjects with OAG or OHT will be randomized to 5 arms: 3 different concentrations of AR-17043, placebo comparator, or netarsudil 0.02% (Rhopressa®) for a treatment duration of 7 days. During Stage 2, approximately 350 adult subjects with OAG or OHT will be randomized to 5 arms: low and high concentrations of PG043 (AR-17043/latanoprost 0.005%), AR-17043 high concentration, latanoprost, or netarsudil 0.02%/latanoprost 0.005% (Rocklatan®) for a treatment duration of 28 days. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT06441643
Study type	Interventional
Source	Alcon Research
Contact	Alcon Call Center
Phone	1-888-451-3937
Email	alcon.medinfo@alcon.com
Status	Not yet recruiting
Phase	Phase 2
Start date	September 2024
Completion date	November 2025

View Details

See also
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