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
Primary listing

Employees

403

NTLA Metrics

BasicAdvanced
$1.5B
-
-$4.68
2.32
-

What the Analysts think about NTLA

Analyst ratings (Buy, Hold, Sell) for Intellia Therapeutics stock.

Bulls say / Bears say

NTLA-2002 Phase 1/2 data demonstrated dramatic, dose-dependent and durable reductions in kallikrein levels suggesting a potential functional cure for hereditary angioedema, and interim Phase 1 results for nex-z showed rapid, deep and durable serum TTR reductions in ATTR patients (Nasdaq).
The FDA granted Regenerative Medicine Advanced Therapy (RMAT) designation to nex-z for ATTR-CM, offering early interactions with the agency and potential priority review of its BLA to accelerate development (GlobeNewswire).
Jones Trading analyst Debanjana Chatterjee believes the FDA clinical hold on Intellia’s Phase 3 trials has limited long-term impact and expects trial activities to resume within a few months (Reuters).
The U.S. FDA placed a clinical hold on Intellia’s two late-stage gene-editing trials after a patient experienced Grade 4 liver enzyme elevations and high bilirubin levels, pausing dosing and screening (Reuters).
Intellia’s stock plummeted 40% after pausing its two Phase 3 clinical trials for nex-z due to a serious safety issue, underscoring significant valuation risk tied to its lead asset (Barron’s).
A January 9, 2025 strategic review led Intellia to discontinue NTLA-3001 and other early-stage programs and reduce its workforce by approximately 27%, narrowing its pipeline and increasing execution risk (Nasdaq).
Data summarised monthly by Lightyear AI. Last updated on 3 Nov 2025.

NTLA Financial Performance

Revenues and expenses
QuarterlyAnnual
Q3 24
QoQ growth
Revenue
$37B
-39.75%
Net income
$45B
107.52%
Profit margin
37.65%
6.78%

NTLA Earnings Performance

Company profitability
QuarterlyAnnual
Q4 23
Q1 24
Q2 24
Q3 24
Q4 24
Actual
$3.69
$2.85
$2.45
$2.42
-
Expected
$3.55
$2.61
$2.05
$2.31
$3.94
Surprise
3.94%
9.20%
19.51%
4.63%
-
Data displayed above is indicative only and its accuracy or completeness is not guaranteed. Actual execution price may vary. Past performance is not indicative of future results. Your return may be affected by currency fluctuations and applicable fees and charges. Capital at risk.
Real-time US market data is sourced from the IEX order book provided by Polygon. After-hours US market data is 15 minutes delayed and may differ significantly from the actual tradable price at market open.

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