Intellia (NASDAQ: NTLA) is a publicly traded Gene & Genome Editing Platforms company founded in 2014 and based in Cambridge, United States.
No dated funding rounds on file. This company is privately held and may be raising or operating on undisclosed capital.
Intellia announces an investor event on lonvo-z and seven presentations at ACAAI 2026.

Intellia's CMO Jing L. Marantz files an initial insider ownership disclosure reporting no securities held.

Intellia grants its medical chief options on 275,061 shares at an $11.26 exercise price.
Lonvo-z, formerly NTLA-2002, is a one-time in vivo CRISPR treatment for hereditary angioedema designed to inactivate the KLKB1 gene in the liver and permanently lower kallikrein and bradykinin levels. In the Phase 3 HAELO trial it reduced attacks by 87% versus placebo over weeks 5 to 28, and 62% of treated patients were free of attacks and of other therapy. The FDA accepted its biologics license application with Priority Review on Sept. 8, 2026 and set a March 10, 2027 action date; Intellia plans a U.S. launch in the first half of 2027.
Nex-z, formerly NTLA-2001, is a one-time in vivo CRISPR treatment for transthyretin (ATTR) amyloidosis designed to inactivate the TTR gene in the liver and stop production of TTR protein. Intellia leads its development with Regeneron in two Phase 3 trials: MAGNITUDE in ATTR amyloidosis with cardiomyopathy and MAGNITUDE-2 in hereditary ATTR amyloidosis with polyneuropathy. Enrollment resumed in the second quarter of 2026 after an FDA clinical hold, and a genomic analysis of more than 600 patient samples linked the highest liver enzyme elevations to one HLA allele.
Intellia's platform combines CRISPR-based gene editing, oligonucleotides and lipid nanoparticles to deliver editing machinery to target tissue through a single intravenous infusion. Lonvo-z and nex-z both use it to knock out a gene in the liver, and the company also runs earlier-stage programs and research collaborations built on the same technologies.
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