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Reading: Sanofi’s SAR446597 earns fast track designation in the US for geographic atrophy due to age-related macular degeneration
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MedEdge MEA > News > Press Releases > Sanofi’s SAR446597 earns fast track designation in the US for geographic atrophy due to age-related macular degeneration
Press Releases

Sanofi’s SAR446597 earns fast track designation in the US for geographic atrophy due to age-related macular degeneration

ME Desk
ME Desk
Published: July 16, 2025
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3 Min Read
Sanofi
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  • Designation earned for a one-time intravitreal gene therapy designed to inhibit two key complement cascade pathways
  • Geographic atrophy is an advanced form of dry age-related macular degeneration, that can lead to permanent vision loss

The US Food and Drug Administration (FDA) has granted fast track designation to SAR446597, a one-time intravitreal gene therapy for the treatment of geographic atrophy (GA) due to age-related macular degeneration (AMD). 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. The FDA created this process to help deliver important new drugs to patients earlier and it covers a broad range of serious illnesses.

Also Read: Sanofi Expands Immunology Footprint with $9.1 Billion Blueprint Medicines Acquisition

SAR446597 delivers genetic material encoding two therapeutic antibody fragments that target and inhibit two critical components of the complement pathway: C1s in the classical pathway and factor Bb in the alternative pathway. This dual-targeting approach potentially offers clinical advantages by providing sustained complement suppression within the retinal microenvironment while significantly reducing treatment burden through elimination of frequent intravitreal injections. The therapy aims to address the underlying pathophysiology of complement-mediated retinal diseases through long-term expression of therapeutic proteins following a single intervention.

Sanofi plans to start a phase 1/2 study to evaluate the safety, tolerability, and efficacy of SAR446597.

Sanofi is also currently evaluating SAR402663, a one-time intravitreal gene therapy, in a phase 1/2 study (clinical study identifier: NCT06660667), for the treatment of patients with neovascular wet age-related macular degeneration.

About age-related macular degeneration and geographic atrophy

AMD is an acquired progressive degeneration of the retina that affects approximately 200 million people globally. Geographic atrophy is an advanced form of dry AMD. It is characterized by enlarging irreversible atrophic lesions due to degeneration of retinal cells leading to permanent vision loss in many patients. GA affects approximately 1 million people in the US, more than 2.5 million in Europe, and over 5 million people worldwide and has a profound impact on quality of life, including ability to read, drive and perform other daily activities.

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