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Intellia Therapeutics/$NTLA

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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
$1.7B
-
-$3.34
1.82
-

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

In Phase 3, a one-off lonvo-z infusion cut hereditary angioedema attacks by 87% versus placebo; 62% of treated patients were attack-free and off preventive therapy during the six-month assessment, against 11% on placebo. This strong result supports the treatment’s potential to offer a major improvement for patients. (Intellia Therapeutics)
The FDA accepted lonvo-z’s application for priority review, set 10 March 2027 as its target decision date and is not currently planning an advisory committee meeting. That gives Intellia a clear near-term regulatory milestone for a possible first-in-class in vivo CRISPR treatment. (SEC)
Intellia reported $628.4 million in cash, equivalents and marketable securities at the end of June, which it expects to fund operations into at least 2028, beyond lonvo-z’s planned US launch. The company says this runway estimate excludes any potential product revenue. (Intellia Therapeutics)
Nex-z’s Phase 3 programme has faced a serious safety setback: a patient developed severe liver toxicity and died, prompting clinical holds and tighter monitoring requirements. The FDA has allowed trials to resume, but the event highlights a material risk to the programme’s safety profile and progress. (BioSpace, Oligonucleotide Therapeutics Society)
Intellia has linked the largest liver-enzyme rises in nex-z patients to a particular HLA allele, and is still discussing the findings with regulators while introducing genotyping in its trials. The safety-management approach is therefore still developing, leaving uncertainty around the ATTR programme. (BioSpace)
Commercial uptake may be harder than the clinical data alone suggest: Barclays argues that existing drugs already serve the HAE and ATTR markets well, and that high-cost treatments have historically been slow to gain traction. That could limit sales expectations for Intellia’s prospective products. (Business Insider)
Data summarised monthly by Lightyear AI. Last updated on 14 Oct 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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