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Efficacy and Safety of AJU-S56 5% in Dry Eye Syndrome Patients

Efficacy and Safety of AJU-S56 5% in Dry Eye Syndrome Patients

Recruiting
19 years and older
All
Phase 3

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Overview

This study is planned to Evaluate the Efficacy and Safety of test drug (AJU-S56 5%) compared to control drug(vehicle) in Patients with Dry Eye Disease.

Eligibility

Inclusion Criteria:

  • Male and Female who over 19 years old
  • Moderate to Severe Dry Eye Disease Patients
  • Must meet all criteria listed below at least in one eye or both eyes.
    1. TCSS (National eye institute (NEI) scale)≥ 4
    2. Ocular discomfort score (ODS) ≥ 3
    3. Schirmer test(without anesthesia) ≤ 10mm in 5 mins
    4. Tear break-up time ≤ 6 secs
  • Written informed consent to participate in the trial

Exclusion Criteria:

  • Those who have clinically significant eye disease not related to dry eye syndrome
  • Those who have worn contact lenses before 1week Screening visit or have to wear contact lenses or need to wear contact lenses during study period
  • Those who have medical history with intraocular surgery 12months before screening visit
  • Use of corticosteroid, beta blocker and anticholinergic agent within 4 weeks
  • Participation in other studies within 4weeks of screening visit

Study details
    Dry Eye Syndromes

NCT06291194

AJU Pharm Co., Ltd.

14 April 2024

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FAQs

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What is a clinical trial?

A clinical trial is a study designed to test specific interventions or treatments' effectiveness and safety, paving the way for new, innovative healthcare solutions.

Why should I take part in a clinical trial?

Participating in a clinical trial provides early access to potentially effective treatments and directly contributes to the healthcare advancements that benefit us all.

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