Why is Intellia Therapeutics stock rallying today?

Intellia Therapeutics (NTLA) announced the FDA accepted and granted priority review to its BLA for lonvoguran ziclumeran, a CRISPR-based therapy for hereditary angioedema (HAE). A decision is expected by March 2027. The therapy showed an 87% reduction in attacks in a phase III study. NTLA shares have risen 41.7% year-to-date. The company also has another CRISPR therapy, nexiguran ziclumeran, in development with Regeneron (REGN).

Intellia Therapeutics' hereditary angioedema treatment, Lonvo-Z, received FDA Priority Review. If approved, it would be the first in vivo CRISPR therapy. The FDA set a PDUFA target action date of March 10, 2027. Lonvo-Z showed an 87% reduction in attacks in a Phase 3 study. Intellia's stock has risen over 35% year-to-date, with ARK Invest recently increasing its stake.

Intellia Therapeutics announced FDA acceptance of its BLA for lonvo-z, a CRISPR-based therapy, with a Priority Review and PDUFA action date of March 10, 2027. The FDA does not plan to hold an advisory committee. If approved, lonvo-z would be the first in vivo CRISPR therapy, supported by Phase 3 data showing an 87% reduction in mean monthly attacks and a 62% attack-free rate.

Intellia Therapeutics (NTLA) shares rose after the FDA granted priority review for its CRISPR-based therapy lonvo-z, targeting hereditary angioedema. The company's P/S ratio is 24.91, below its historical median, suggesting market expectations of future growth. GuruFocus' GF Value™ estimates NTLA is 4.8% undervalued at $12.63 per share, with a GF Score™ of 70/100.

Intellia Therapeutics (NTLA) received FDA Priority Review for lonvo-z, a CRISPR-based therapy for hereditary angioedema, with a decision expected by March 2027. The company's P/S ratio is 25.13, below its historical median of 32.3x, and its GF Value™ suggests it is 4.0% undervalued. Insider activity shows net selling, while six top gurus hold the stock, with mixed recent activity.

Intellia Therapeutics (NTLA) shares rose 8% after the FDA accepted its Biologics License Application with Priority Review for lonvoguran ziclumeran (lonvo-z) for hereditary angioedema. The FDA set a target action date of March 10, 2027. The application is supported by Phase 3 trial data showing an 87% reduction in mean monthly attacks compared with placebo. If approved, lonvo-z would be the first in vivo CRISPR-based therapy for HAE.