Commentary|Articles|October 14, 2026

FAQ: What clinicians should know as SYD-101 heads to FDA advisory committee

Fact checked by: Nimesh Patel, MD

FDA advisers review SYD-101, low-dose atropine 0.01% for pediatric myopia, on Oct 30 after a 2025 complete response letter.

The US FDA Dermatologic and Ophthalmic Drugs Advisory Committee will meet October 30, 2026, to review new drug application (NDA) 219694 for SYD-101 (atropine sulfate ophthalmic solution 0.01%; Sydnexis), proposed for slowing myopia progression in children aged 3 years or older.1

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