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โ† Trials
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Evaluation of the Safety and Efficacy of GLK-321 in Subjects With Demodex Blepharitis

RecruitingPhase 2Ages 18 Years - anyAllGlaukos Corporation
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In plain words

What the trial is, and whether it could suit you

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.

Sign in to get the eligibility rules as simple questions to take to your doctor.

๐Ÿ“‹ Eligibility rules (as published)
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 Screening * Active ocular infection or inflammation, other than blepharitis, in either eye at Screening * Women who are pregnant, planning a pregnancy, or nursing * Have used an investigational drug or device within 30 days prior to Screening or concurrently enrolled in another investigational drug or device trial
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What it tests

  • GLK-321 low dose BID
  • GLK-321 mid dose BID
  • GLK-321 high dose BID
  • GLK-321 high dose QD
  • Placebo BID
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Where

1 site
Glaukos Clinical Study Site
Newport Beach, United States
๐Ÿค Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible โ€” always decide together with your own doctor.
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