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Cathie Wood's Biotech Bet Intellia Secured An FDA Priority Review For Rare Genetic ...

Published

8 September 2026

Topic

opportunities

Sectors

Biotech

Geography

United States

Source

Read at finance.yahoo.com

Verified

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.

◆ The Wire takeaway

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.

Coverage

2 sources · 8 Sep 2026

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Biotechfdapriority-reviewgene-editingrare-diseasebiotech