Evaluation of the Safety and Efficacy of GLK-321 in Subjects With Demodex Blepharitis

Recruiting Phase 2 Interventional Study
Demodex Blepharitis
Prior Safety Data This treatment has already been tested in at least one earlier human trial.
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At a Glance
Age
18 and older
Sex
Any
Trial phase
Phase 2
Study type
Interventional
Purpose
Treatment
Participants needed
250 (estimated)
Sponsor
Glaukos Corporation · Industry
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About This Trial

This is a randomized, double-masked, placebo-controlled, dose-ranging, parallel-group, multi-center study designed to evaluate the safety and efficacy of GLK-321 in patients with Demodex blepharitis.

Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Signs of Demodex blepharitis in at least one eye * Best Spectacle Corrected Visual Acuity (BSCVA) of 20/80 Snellen or better in each eye Exclusion Criteria: * Presence of eczema or dermatitis in the ocular region of either eye * Use of lid hygiene products within 14 days of …
Contacts

Study Manager

949-739-8749

ClinicalResearch@Glaukos.com

CONTACT