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FDA committee considers SYD-101 for pediatric myopia

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FDA advisory committee reviews SYD-101 atropine eye drops for pediatric myopia

An FDA advisory committee convened on October 30 to discuss SYD-101, a low-dose atropine eye drop for slowing pediatric myopia that the FDA declined to approve last year. The treatment met its primary endpoint in a phase 3 trial, but the FDA determined the overall results were insufficient for approval.

Oct 30, 2026·1 sourceChild healthFDA drug approvalDrug Policy, Pricing & ApprovalOphthalmic topicalClinical trial endpointsCompounding pharmaciesDrug development
FDA advisory committee reviews SYD-101 atropine eye drops for pediatric myopia
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