Trial Profile

A Multicenter, Double-Masked, Randomized, Placebo-Controlled Phase 3 Study of the Safety and Efficacy of Atropine 0.1% and 0.01% Ophthalmic Solutions Administered With a Microdose Dispenser for the Reduction of Pediatric Myopia Progression (The CHAPERONE Study)

Status: Discontinued

Phase of Trial: Phase III

Latest Information Update: 08 Jan 2025

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At a glance

06 Jan 2025 Status changed from active, no longer recruiting to discontinued.
20 Nov 2024 Status changed from recruiting to active, no longer recruiting.
15 Nov 2024 According to an Eyenovia media release, company announced that a review of the CHAPERONE data by an independent Data Review Committee (DRC) found that the trial is not meeting its primary endpoint of a less than 0.5 diopter progression in visual acuity over three years.

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