Quoin Pharmaceuticals Ltd. has filed an application for Breakthrough Medicine Designation with the Saudi Food and Drug Authority (SFDA) for QRX003, its lead investigational topical product for the treatment of Netherton Syndrome. If the designation is granted, QRX003 could become the first approved treatment for Netherton Syndrome and may be available for sale and reimbursement in Saudi Arabia in the second half of 2026. QRX003 is currently being evaluated in two late-stage clinical trials, with enrollment expected to be completed in the first half of 2026 and top-line data anticipated in the second half of the year. Quoin also plans to submit a New Drug Application in the United States and other territories pending successful clinical outcomes.

Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Quoin Pharmaceuticals Ltd. published the original content used to generate this news brief via GlobeNewswire (Ref. ID: GNW9628343-en) on January 20, 2026, and is solely responsible for the information contained therein.