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ATSN-510 is an undisclosed adeno-associated virus (AAV) gene therapy candidate being developed by Atsena Therapeutics. It is part of the company's discovery-stage pipeline focused on treating inherited retinal diseases, which cause progressive and irreversible vision loss. Atsena Therapeutics utilizes its proprietary AAV technology platform to design and develop gene therapies that can overcome the unique anatomical and physiological barriers of the eye.
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