FDA accepts IND application to begin Eyenovia myopia study

Eyenovia announced the FDA accepted an investigational new drug application to initiate a phase 3 registration trial of MicroPine to reduce the progression of myopia in children.
According to a company press release, the U.S.-based, multicenter, randomized, double-masked CHAPERONE study will include 400 children between 5 and 12 years old. Participants will be randomly assigned to receive one of two MicroPine treatment concentrations or a placebo.
“The American Academy of Ophthalmology recently cited Level 1 evidence that topical lower doses of atropine treatment have demonstrated robust

Full Story →