Utilizing Gene Therapy and Viral Vector Delivery as a Potential "One-Time" Cure within the Thyroid Eye Disease Sector for Late 2025

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2025-12-24 13:56:50 -

Perhaps the most ambitious frontier in late 2025 is the development of gene therapies for thyroid eye disease. Rather than requiring lifelong medication or repeated infusions, these experimental programs aim to "reprogram" the cells behind the eye to stop the inflammatory process permanently. Using AAV-based vectors delivered via a local injection around the eye, researchers are attempting to...

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