PARIS (dpa-AFX) - Sanofi said the FDA has granted fast track designation to SAR402663, an investigational one-time intravitreal gene therapy for the treatment of neovascular age-related macular degeneration. Sanofi is currently evaluating SAR402663 in a phase 1/2 for the treatment of patients with neovascular AMD. SAR402663 delivers genetic material encoding soluble FLT01 designed to inhibit vascular endothelial growth factor.
The fast-track designation process aims to facilitate the development and expedite the review of medicines to treat serious conditions and fill unmet medical need.
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