Clinical Trial

Moderate-to-Severe Dry Eye Disease Relief Using Acoltremon

Study acronym: ASTRA
Enrolling by Invitation
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Summary
To evaluate the impact of Acoltremon 0.003% on subjective dry eye symptoms using validated patient-reported outcome measures: Eye Dryness Score Visual Analog Scale (EDS-VAS). The primary aim is to characterize the rapidity of symptomatic relief in moderate to severe dry eye disease (DED), with attention to short-term therapy.
Trial Details
NCT Number NCT07268599
Lead Sponsor Colvard Kandavel Eye Center
Conditions Dry Eye Disease (DED)
Enrollment 50 participants
Start Date 2025-11-24
Primary Completion 2026-10 (estimated)
Study Completion 2026-10 (estimated)
Updated on ClinicalTrials.gov 2025-12-08