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AIRNA develops a proprietary RNA editing platform to create genetic medicines aimed at providing functional cures. Its lead program, AIR‑001, targets alpha‑1 antitrypsin deficiency by repairing mutations in the SERPINA1 gene. The company recently raised $155M Series B funding to support a Phase I/II trial of AIR‑001 and expand its pipeline into cardiometabolic and other diseases. No published clinical results yet; first-in-human studies are imminent or just starting.
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