Intellia Therapeutics/$NTLA

Intellia shares rise after the FDA accepted lonvo-z’s BLA for priority review, supported by positive Phase 3 HAELO data showing an 87% reduction in hereditary angioedema attacks after one dose.
1 hour agoLightyear AI
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About Intellia Therapeutics

Intellia Therapeutics is a gene-editing company focused on the development of Crispr/Cas9-based therapeutics. Crispr/Cas9 stands for Clustered Regularly Interspaced Short Palindromic Repeats (Crispr)/Crispr-associated protein 9 (Cas9), which is a revolutionary technology for precisely altering specific sequences of genomic DNA. Intellia is focused on using this technology to treat genetically defined diseases. It's evaluating multiple gene editing approaches using in vivo and ex vivo therapies to address diseases with high unmet medical needs, including ATTR amyloidosis, hereditary angioedema, sickle cell disease, and immuno-oncology. Intellia has formed collaborations with several companies to advance its pipeline, including narrow-moat Regeneron and wide-moat Novartis.
Ticker
$NTLA
Sector
Health
Primary listing
NASDAQ
Employees
377

NTLA Metrics

BasicAdvanced
$1.6B
-
-$3.34
1.79
-

What the Analysts think about NTLA

Analyst ratings (Buy, Hold, Sell) for Intellia Therapeutics stock.
Analyst projections of the future price of Intellia Therapeutics stock.

Bulls say / Bears say

Lonvo-z produced strong Phase 3 HAELO results. A single infusion cut mean monthly hereditary angioedema attacks by 87% versus placebo, and 62% of treated patients were both attack-free and free of HAE therapy over six months, compared with 11% on placebo. (GlobeNewswire, Markets Insider)
The FDA has accepted lonvo-z’s BLA for Priority Review and set a 10 March 2027 decision date, with no advisory committee currently planned. If approved, it would be the first in-vivo CRISPR therapy and the only one-time HAE treatment, creating a clear near-term catalyst and potential first-mover advantage. (Investing News Network, Markets Insider)
Intellia ended June with $628.4 million in cash, cash equivalents and marketable securities, which management expects to fund operations at least into 2028 without counting lonvo-z revenue. A new OrbiMed facility can add up to $400 million, helping fund the planned launch and ongoing ATTR trials without an immediate share issue. (GlobeNewswire, BioSpace)
Nex-z’s ATTR programme still carries a safety overhang. Intellia found an HLA allele linked to liver-enzyme elevations, leading to HLA typing and tighter monitoring after the Phase 3 trials resumed. (The Motley Fool, GlobeNewswire)
Intellia remains loss-making and has already relied on financing to fund its next phase. The April share offering raised about $195 million, while the Q2 net loss was $106.6 million; continued spending could mean further dilution or borrowing before products generate revenue. (GlobeNewswire, TradingKey)
Lonvo-z still faces clinical and regulatory uncertainty despite the BLA acceptance. The pivotal HAELO trial involved only 80 patients and reported its main comparison over six months, while FDA acceptance and Priority Review do not guarantee approval or prove long-term durability. (Markets Insider, GlobeNewswire)
Data summarised monthly by Lightyear AI. Last updated on 17 Sept 2026.

NTLA Financial Performance

Revenues and expenses
Income statement
QuarterlyAnnual
Q3 24
QoQ growth
Revenue
Net income
Profit margin

NTLA Earnings Performance

Company profitability
Earnings per share
QuarterlyAnnual
Q4 23
Q1 24
Q2 24
Q3 24
Q4 24
Actual
Expected
Surprise
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