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Cathie Wood's Biotech Bet Intellia Secured An FDA Priority Review For Rare Genetic ...
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Fusion42 · 8 September 2026 · Fusion42 review
The FDA granted priority review to Intellia Therapeutics' gene-editing therapy lonvoguran Ziclumeran for a rare genetic disorder, hereditary angioedema, with a decision due by March 10, 2027. Intellia's trial showed significant reduction in attacks and no serious adverse events, marking a potential first for in vivo CRISPR therapy.
This Wire brief sits within Fusion42's coverage of Biotech, and 2 sources have reported it.
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FDA priority review fast-tracks gene-editing therapy approval deadlines and opens a clear regulatory path for in vivo CRISPR treatments. You can now plan commercial and clinical strategies with more confidence around this timing and regulatory support.
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2 sources · 8 Sep 2026
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