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Study identifier: NCT03942419 Synced from ClinicalTrials.gov · July 30, 2026
● Terminated

Microdosed Atropine 0.1% and 0.01% Ophthalmic Solutions for Reduction of Pediatric Myopia Progression

Condition: Myopia  ·  Sponsor: Eyenovia Inc.

PhasePhase 3
Planned participants438
Who can joinAll sexes, 3 Years to 12 Years
Healthy volunteersNo

About this study

This study evaluates the progression of myopia in participants using microdosed atropine 0.01%, atropine 0.1%, or placebo ophthalmic solution. Eligible subjects will administer study medication daily in each eye for 48 months. Efficacy and safety assessments will be performed at visits scheduled for 1, 6, 12, 18, 24, 30 and 36 months after initiation of medication use. Subjects will be re-randomized at the 36 month visit, then followed at 6 month intervals for an additional year.

This description comes directly from the study's public registry record.

Talk to the study team

Contact details are listed per location below or on the registry record.

Always discuss trial participation with your own doctor first.

Locations (18)

University of Alabama at Birmingham School of OptometryBirmingham, Alabama, United States
Midwestern UniversityGlendale, Arizona, United States
Canyon City EyecareAzusa, California, United States
UC BerkeleyBerkeley, California, United States
Marshall Ketchum University College of OptometryLos Angeles, California, United States
Ratner Children's Eye CenterSan Diego, California, United States
Illinois College of OptometryChicago, Illinois, United States
Midwestern UniversityDowners Grove, Illinois, United States
SUNY College of OptometryNew York, New York, United States
Wake Forest Health Network Ophthalmology - Oak HollowHigh Point, North Carolina, United States
Oculus ResearchRaleigh, North Carolina, United States
The Ohio State University - College of OptometryColumbus, Ohio, United States

+ 6 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT03942419