The race to develop new therapies that precisely edit short-lived RNA molecules instead of making irreversible changes to DNA is heating up. A new entrant to the growing field emerged from stealth Tuesday morning with a $30 million initial financing round led by ARCH Venture Partners to make RNA editing therapies for both rare and common diseases.
The startup, called AIRNA, was co-founded in 2021 by Thorsten Stafforst — a University of Tübingen biochemist whose work over the past decade helped spark interest in RNA editing therapies — and Jin Billy Li, a Stanford University biologist who has studied the enzymes that power RNA editing in nature since 2006.
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