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Ascidian Therapeutics Launches to Rewrite RNA

Sea creature-inspired biotech Ascidian surfaces with $50M and a new way to edit RNA

Ascidian Therapeutics is developing therapies for inherited disorders that work by editing RNA with an approach that could offer advantages over currently available genetic medicines. The biotech’s lead program is in preclinical development for Stargardt disease, a rare eye disorder caused by multiple genetic mutations.

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