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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)

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

  • Drugs Atropine (Primary)
  • Indications Myopia
  • Focus Registrational; Therapeutic Use
  • Acronyms CHAPERONE
  • Sponsors Bausch & Lomb; Eyenovia

Most Recent Events

  • 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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