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NTLA Overview

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0.000(0.000%)
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0.000(0.000%)Aft-market
ET
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0.000
0.000(0.000%)
At close
0.000(0.000%)Aft-market
ET
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Intellectia

Loading chart...

High
15.910
Open
15.450
VWAP
15.48
Vol
4.31M
Mkt Cap
1.81B
Low
15.220
Amount
66.74M
EV/EBITDA(TTM)
--
Total Shares
118.13M
EV
1.35B
EV/OCF(TTM)
--
P/S(TTM)
24.35
Intellia Therapeutics, Inc. is a clinical-stage gene editing company focused on developing medicine with CRISPR-based therapies and other core technologies. CRISPR/Cas9 is a gene editing technology that leverages the body’s natural processes to precisely edit DNA. The Company is developing lonvoguran ziclumeran (lonvo-z), referred to as NTLA-2002, for the treatment of hereditary angioedema (HAE) and nexiguran ziclumeran (nex-z) also referred to as NTLA-2001, for the treatment of transthyretin (ATTR) amyloidosis. It is focused on completing late-stage clinical development of its lead product candidates, lonvo-z for the treatment of patients with HAE and nex-z for the treatment of patients with ATTR amyloidosis with cardiomyopathy (ATTR-CM) and hereditary ATTR amyloidosis with polyneuropathy (ATTRv-PN). Its lead product candidates are the first in vivo genome editing product candidates into Phase III development. Its other pipeline products include REGV131-LNP1265 and AVC-201 & AVC-203.
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Events Timeline

(ET)
2026-03-03
07:50:00
Intellia Therapeutics Presents Hereditary Angioedema Study Results
select

News

Fool
6.5
04-15Fool
Analysis of Investment Prospects in Healthcare Stocks
  • Animal Health Leader: Zoetis has faced challenges over the past two years, including increased competition and scrutiny over drug side effects; however, its strong market position and the potential market for untreated dogs make it attractive for long-term investors, with expectations to continue launching new products to meet rising pet spending.
  • New Drug Development Potential: BioNTech has underperformed in the coronavirus vaccine market, but its impressive pipeline with over 25 clinical trials in oncology, particularly the promising BNT327 developed with Bristol Myers Squibb, could set new standards of care across multiple indications, with significant clinical and regulatory progress expected over the next five years.
  • Gene Editing Risks: Intellia Therapeutics' lonvo-z and nex-z are undergoing phase 3 studies but face uncertainty; despite the FDA lifting the hold on clinical trials, the high costs and complexities of gene editing treatments make steady revenue generation unlikely in the coming years, presenting substantial investment risks.
  • Dividend Appeal: Zoetis has increased its dividends by 458% over the past decade, making it a top choice for income-seeking investors, reflecting its long-term investment value in the animal health market despite facing short-term challenges.
Yahoo Finance
3.5
04-12Yahoo Finance
Gene Drive Technology as a Solution to Invasive Species
  • Global Economic Impact: According to Ben Lamm, CEO of Colossal Biosciences, invasive species result in a staggering $5.4 trillion in global economic losses, with the U.S. alone suffering over $500 billion annually, highlighting the urgent need for effective control methods.
  • Humane Solution: Colossal's gene drive technology proposes using genetically modified invasive animals that produce only male offspring, eliminating the need for mass culling and poison, showcasing a more humane approach that also offers reversibility, a feature lacking in traditional methods.
  • Market Potential: Companies like CRISPR Therapeutics, Beam Therapeutics, and Intellia Therapeutics are positioning their genome editing platforms as foundational infrastructure for gene drive applications, which could significantly expand their market potential beyond rare disease therapeutics if regulatory acceptance is achieved.
  • Commercial Opportunity: Lamm noted that Texas has declared the screwworm a national emergency, indicating a substantial commercial opportunity in invasive species control that could yield billions for related companies, especially if gene drive technology becomes the standard.
Newsfilter
8.5
04-08Newsfilter
Biotech IPOs Show Strong Performance in Q1 2026
  • Biotech Financing Trends: In Q1 2026, biotech companies raised a median of $287.5 million each, with nearly all possessing mid to late-stage clinical data, indicating a strong market focus on high-value science that boosts investor confidence and capital inflow.
  • Industry Focus on High-Value Projects: The IQVIA report reveals that pharmaceutical R&D spending reached $159.1 billion in 2025, with companies redirecting resources toward validated late-stage programs, reflecting a market preference for credible pipelines that enhances the standing of biotech firms.
  • Avaí Bio's Major Progress: Avaí Bio is set to present new data on its α-Klotho anti-aging therapy at the Second Annual Klotho Conference, being invited to speak alongside renowned researchers, which signifies an elevation in its influence within the Klotho space and may attract increased investor attention.
  • Stoke Therapeutics' Breakthrough Results: Stoke Therapeutics published data on zorevunersen in The New England Journal of Medicine, demonstrating its potential disease-modifying effects in Dravet syndrome, which is expected to propel its Phase 3 EMPEROR study in 2027, further solidifying its market position.
NASDAQ.COM
8.5
03-08NASDAQ.COM
Intellia Therapeutics Overcomes Regulatory Setback
  • Clinical Study Resumption: The FDA has lifted the clinical hold on Intellia Therapeutics' nex-z drug, allowing it to proceed with Phase 3 studies, a development that could drive stock recovery despite last year's price drop due to a patient death incident.
  • Drug Potential Analysis: As a treatment for transthyretin amyloidosis, nex-z is expected to offer a one-time solution for hundreds of thousands of patients worldwide, and successful commercialization could significantly enhance Intellia's market position in the biotech sector.
  • Risk Management Measures: The company plans to exclude patients with liver issues in late-stage studies of nex-z and will closely monitor liver inflammation, yet potential safety concerns may still hinder market acceptance.
  • Market Competitive Landscape: While Intellia's partnership with Regeneron provides technical support, the high costs and complexities of gene editing drugs remain major barriers to commercialization, prompting investors to carefully assess future performance.
Fool
8.5
03-08Fool
Analysis of Intellia Therapeutics' Stock Price Recovery
  • Stock Recovery: Intellia Therapeutics' stock has surged 47% over the past year, rebounding to $13.41 per share, reflecting increased market confidence in its innovative potential and future growth prospects.
  • Clinical Progress: The FDA has lifted clinical holds on nex-z, allowing Intellia to advance its treatments for transthyretin amyloidosis and hereditary angioedema, marking a significant step in addressing previous setbacks.
  • Risk Warning: Despite positive developments, the unclear causal relationship between nex-z and a patient's death raises concerns about potential future challenges in clinical trials, increasing investor apprehension.
  • Market Potential: As a one-time treatment option, nex-z targets hundreds of thousands of patients with transthyretin amyloidosis globally, which could significantly reshape the market landscape if successfully launched, though high R&D costs and complex administration remain major hurdles.
Yahoo Finance
8.5
03-08Yahoo Finance
Cathie Wood's Intellia Therapeutics Surges 47%: Is It Too Late to Invest?
  • Stock Performance: Intellia Therapeutics has seen a 47% increase in its stock price this year, reflecting strong market confidence in its gene-editing drugs, particularly after the FDA lifted clinical holds on nex-z, leading investors to be optimistic about its future prospects.
  • Clinical Progress: The FDA's lifting of clinical holds on nex-z allows Intellia to advance its treatment for hereditary angioedema, a development that not only helps restore investor confidence but also has the potential to generate new revenue streams for the company.
  • Risk Factors: Despite the positive developments, Intellia faces potential safety concerns, especially since the causal relationship between nex-z and a patient's death remains unclear, which could complicate future clinical trials and increase investment uncertainty.
  • Market Competition: Intellia's partnership with Regeneron provides robust support for the development of nex-z, yet the high costs and complexities associated with gene-editing drugs remain significant barriers to market adoption, potentially limiting its acceptance among third-party payers.
Wall Street analysts forecast NTLA stock price to rise
22 Analyst Rating
Wall Street analysts forecast NTLA stock price to rise
9 Buy
12 Hold
1 Sell
Moderate Buy
Current: 0.000
sliders
Low
4.00
Averages
16.50
High
54.00
Current: 0.000
sliders
Low
4.00
Averages
16.50
High
54.00
JonesResearch
Hold
to
Buy
upgrade
$29
AI Analysis
2026-03-04
Reason
JonesResearch
Price Target
$29
AI Analysis
2026-03-04
upgrade
Hold
to
Buy
Reason
JonesResearch upgraded Intellia Therapeutics to Buy from Hold with a $29 price target. The The FDA removed the hold on both MAGNITUDE and MAGNITUDE-2 studies, with Intellia reactivating sites to continue enrollment, the analyst tells investors in a research note. The firm says clarity around the cause of death being likely unrelated to nex-z and favorable regulatory updates reinstate its bullish view on the shares.
BofA
Alec Stranahan
Neutral
maintain
$17 -> $19
2026-03-03
Reason
BofA
Alec Stranahan
Price Target
$17 -> $19
2026-03-03
maintain
Neutral
Reason
BofA analyst Alec Stranahan raised the firm's price target on Intellia Therapeutics to $19 from $17 and keeps a Neutral rating on the shares. The FDA has removed the clinical hold on the MAGNITUDE Phase 3 study in transthyretin amyloidosis-cardiomyopathy for nex-z, re-opening the "larger value driver in the franchise," the analyst tells investors. Following the news, the firm increased its view of the probability of success in ATTR-CM to 55% from 38%.
Unlock Full Analyst Thesis, Get the complete breakdown of rating reason for NTLA
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Valuation Metrics

The current forward P/E ratio for Intellia Therapeutics Inc (NTLA.O) is 0.00, compared to its 5-year average forward P/E of -10.37. For a more detailed relative valuation and DCF analysis to assess Intellia Therapeutics Inc's fair value, Click here.

Forward PE

The forward P/E ratio is a valuation metric that divides a company's current stock price by its estimated future earnings per share over the next 12 months.
StronglyUndervaluedUndervaluedFairOvervaluedStronglyOvervalueddotted line Image
N/A
5Y Average PE
-10.37
Current PE
0.00
Overvalued PE
0.81
Undervalued PE
-21.56

Forward EV/EBITDA

The forward EV/EBITDA ratio is a valuation metric that divides a company's enterprise value (EV) by its estimated future earnings before interest, taxes, depreciation, and amortization (EBITDA) over the next 12 months.
StronglyUndervaluedUndervaluedFairOvervaluedStronglyOvervalueddotted line Image
N/A
5Y Average EV/EBITDA
-7.39
Current EV/EBITDA
-1.67
Overvalued EV/EBITDA
1.53
Undervalued EV/EBITDA
-16.30

Forward PS

The forward P/S ratio is a valuation metric that divides a company's current stock price by its estimated future sales (or revenue) per share over the next 12 months.
StronglyUndervaluedUndervaluedFairOvervaluedStronglyOvervalueddotted line Image
5Y Average PS
82.10
Current PS
7.36
Overvalued PS
160.20
Undervalued PS
4.01

Financials

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Whales Holding NTLA

H
Himension Capital (Singapore) Pte Ltd
Holding
NTLA
+8.76%
3M Return
A
ARK Investment Management LLC
Holding
NTLA
+3.42%
3M Return

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Frequently Asked Questions

What is Intellia Therapeutics Inc (NTLA) stock price today?

The current price of NTLA is 15.31 USD — it has increased 0.66

What is Intellia Therapeutics Inc (NTLA)'s business?

Intellia Therapeutics, Inc. is a clinical-stage gene editing company focused on developing medicine with CRISPR-based therapies and other core technologies. CRISPR/Cas9 is a gene editing technology that leverages the body’s natural processes to precisely edit DNA. The Company is developing lonvoguran ziclumeran (lonvo-z), referred to as NTLA-2002, for the treatment of hereditary angioedema (HAE) and nexiguran ziclumeran (nex-z) also referred to as NTLA-2001, for the treatment of transthyretin (ATTR) amyloidosis. It is focused on completing late-stage clinical development of its lead product candidates, lonvo-z for the treatment of patients with HAE and nex-z for the treatment of patients with ATTR amyloidosis with cardiomyopathy (ATTR-CM) and hereditary ATTR amyloidosis with polyneuropathy (ATTRv-PN). Its lead product candidates are the first in vivo genome editing product candidates into Phase III development. Its other pipeline products include REGV131-LNP1265 and AVC-201 & AVC-203.

What is the price predicton of NTLA Stock?

Wall Street analysts forecast NTLA stock price to rise over the next 12 months. According to Wall Street analysts, the average 1-year price target for NTLA is16.50 USD with a low forecast of 4.00 USD and a high forecast of 54.00 USD. However, analyst price targets are subjective and often lag stock prices, so investors should focus on the objective reasons behind analyst rating changes, which better reflect the company's fundamentals.

What is Intellia Therapeutics Inc (NTLA)'s revenue for the last quarter?

Intellia Therapeutics Inc revenue for the last quarter amounts to 23.02M USD, increased 78.79

What is Intellia Therapeutics Inc (NTLA)'s earnings per share (EPS) for the last quarter?

Intellia Therapeutics Inc. EPS for the last quarter amounts to -0.83 USD, decreased -34.65

How many employees does Intellia Therapeutics Inc (NTLA). have?

Intellia Therapeutics Inc (NTLA) has 377 emplpoyees as of April 22 2026.

What is Intellia Therapeutics Inc (NTLA) market cap?

Today NTLA has the market capitalization of 1.81B USD.