Intellia Therapeutics, Inc. (NTLA) Stock Price & How to Invest
Short answer
You can invest in Intellia Therapeutics (NTLA) by buying shares or fractional shares at any major broker, through an ETF that holds it, or as one holding in a thematic basket. NTLA is a clinical-stage CRISPR gene-editing biotech whose thesis rests on its in vivo platform, which edits genes directly inside the body, and two late-stage candidates: lonvo-z for hereditary angioedema and nex-z for ATTR amyloidosis, the latter partnered with Regeneron. The biggest risk is that the company is pre-revenue and unprofitable, its value is tied to binary clinical-trial and regulatory outcomes, and it funds operations through cash reserves that periodically require dilutive equity raises.
NTLA stock price
As of 2026-06-26, Intellia Therapeutics, Inc. (NTLA) last closed at $16.68, up 74.5% over the past year. Over the past 52 weeks it has traded between $8.04 and $27.98.
Prices are daily closing prices from Yahoo Finance and may be delayed. For the live quote, check your broker or Intellia Therapeutics, Inc.'s investor relations page. Walnut is informational, not investment advice.
What does Intellia Therapeutics, Inc. (NTLA) do?
Intellia Therapeutics, Inc. is a clinical-stage biotechnology company headquartered in Cambridge, Massachusetts, developing genome-editing therapies based on CRISPR/Cas9. Its core differentiator is a proprietary in vivo platform that delivers the editing machinery directly into the body, typically the liver, using lipid nanoparticles, so that a single dose can permanently inactivate or modify a disease-causing gene without removing cells from the patient. This contrasts with ex vivo approaches that edit cells outside the body and reinfuse them. The company is pre-revenue from products and currently records only collaboration revenue from partners; it funds operations through its cash reserves and periodic capital raises.
Intellia was co-founded in 2014, drawing on foundational CRISPR research associated with Nobel laureate Jennifer Doudna, and went public on the Nasdaq in 2016. Its two most advanced wholly described programs are lonvoguran ziclumeran (lonvo-z, formerly NTLA-2002) for hereditary angioedema and nexiguran ziclumeran (nex-z, formerly NTLA-2001) for transthyretin (ATTR) amyloidosis, the latter developed in collaboration with Regeneron Pharmaceuticals. In 2025 the company prioritized these late-stage assets through a strategic reorganization. As of mid-2026, lonvo-z had reported positive Phase 3 HAELO results and entered rolling FDA biologics license application review, while the nex-z Phase 3 MAGNITUDE and MAGNITUDE-2 trials in ATTR were advancing after the FDA lifted earlier clinical holds.
What's driving Intellia Therapeutics, Inc. (NTLA)?
Positive Late-Stage Lonvo-z Data in Hereditary Angioedema
In 2026 Intellia reported positive Phase 3 HAELO results for lonvo-z in hereditary angioedema, including an approximately 87 percent reduction in mean monthly attacks versus placebo, with a majority of treated patients reported as attack-free over the efficacy period. The data were published in the New England Journal of Medicine and presented at EAACI 2026. The company has begun a rolling FDA biologics license application, positioning lonvo-z as a potential one-time treatment with a possible U.S. launch in 2027.
In Vivo CRISPR Platform
Intellia's central asset is its in vivo editing platform, which aims to make a single-dose, durable genetic change inside the patient's body rather than through cells edited in a lab. If validated across multiple programs, this approach could be applied to a range of genetic and acquired diseases. The same delivery and editing technology underlies both lead candidates, so platform validation in one indication carries read-through to the broader pipeline.
Regeneron Partnership and Nex-z in ATTR Amyloidosis
The nex-z program for ATTR amyloidosis is developed with Regeneron Pharmaceuticals, which shares development costs and provides a large-pharma partner. In early 2026 the FDA lifted clinical holds on the Phase 3 MAGNITUDE (cardiomyopathy) and MAGNITUDE-2 (polyneuropathy) trials, with MAGNITUDE-2 enrollment targeted for the second half of 2026. ATTR amyloidosis is a large and growing market currently served by approved stabilizer and silencer drugs from other companies.
Large Addressable Disease Areas
Both lead programs target serious diseases with meaningful patient populations and high unmet need where a single-dose therapy could be differentiated from chronic treatments. Hereditary angioedema patients currently rely on lifelong prophylaxis, and ATTR amyloidosis is an underdiagnosed, progressive condition. A durable one-time editing approach, if approved and adopted, could address both the clinical burden and the cumulative cost of chronic therapy, though commercial success is not assured.
What are the risks to Intellia Therapeutics, Inc. (NTLA)?
Intellia is pre-revenue from products, deeply unprofitable, and its value depends on binary clinical and regulatory outcomes; a single failed trial, safety signal, or FDA setback for lonvo-z or nex-z could sharply reduce the stock's value. The company burns roughly $90 million to $100 million per quarter and has repeatedly raised equity to extend its runway, so existing shareholders face ongoing dilution risk before any product profit materializes. Even with positive data, regulatory approval, reimbursement, and commercial adoption of a novel one-time gene-editing therapy are uncertain and could take years. The company also competes with better-capitalized CRISPR and gene-editing peers, with RNA-interference and stabilizer drugs already approved in ATTR, and with established prophylaxis options in hereditary angioedema.
How is Intellia Therapeutics, Inc. (NTLA) valued? (approximate, June 27, 2026 (data reflects most recently available reports through mid-2026))
A simple financial snapshot. These are approximations and refresh quarterly; for current figures see Intellia Therapeutics, Inc.'s investor relations page or your broker.
- Cash and Marketable Securities: ~$517 million (as of March 31, 2026), plus ~$207 million gross from an April 2026 equity offering
- Stated Cash Runway: Expected to fund operations at least into 2028
- Net Loss (Q1 2026): ~$96 million (versus ~$114 million in Q1 2025)
- Revenue: Collaboration revenue only (e.g., Regeneron); no product revenue yet
- Market Capitalization: ~$1.7 billion (June 2026, moves sharply on clinical news)
- P/E Ratio (TTM): Negative (not meaningful; company is unprofitable)
Because Intellia has no product profits and only collaboration revenue, traditional earnings-based valuation multiples like P/E are negative and not analytically useful. The stock is better evaluated on its cash runway relative to its burn rate, the probability and timing of regulatory approval for lonvo-z and nex-z, and the risk-adjusted commercial potential of those programs. The April 2026 equity raise extended the stated runway at least into 2028, but pre-profit biotechs of this type typically require additional capital before reaching sustained profitability, so dilution and the binary nature of trial readouts are central to any valuation view.
Which ETFs hold Intellia Therapeutics, Inc. (NTLA)?
If you want NTLA exposure as part of a larger bundle rather than directly, these ETFs hold it meaningfully. Weights are approximate and refresh quarterly.
| ETF | Name | % in NTLA | Expense ratio | |
|---|---|---|---|---|
| ARKG | ARK Genomic Revolution ETF | approximately 5% | 0.75% |
Who competes with Intellia Therapeutics, Inc. (NTLA)?
Pure-Play CRISPR Gene-Editing Companies
CRISPR Therapeutics (CRSP) is the most directly comparable peer and the only CRISPR-focused biotech with an approved product, Casgevy, co-developed with Vertex for sickle cell disease and beta-thalassemia; it held roughly $2.4 billion in cash as of early 2026, a stronger balance sheet than Intellia. Editas Medicine (EDIT) is a smaller founding-era CRISPR peer that has refocused on in vivo development candidates. These companies share Intellia's foundational ambition and compete for capital, talent, and clinical priority.
Base Editing and Next-Generation Editing Platforms
Beam Therapeutics (BEAM) pursues base editing, a CRISPR variant that makes single-nucleotide changes without cutting both DNA strands, and held roughly $1.2 billion in cash as of early 2026 while advancing programs in sickle cell disease and other rare conditions. Prime Medicine develops prime editing for precise gene correction. These platforms compete for the same disease targets and investor attention, though none has yet reached commercial approval.
Established Therapies in Intellia's Target Indications
In ATTR amyloidosis, nex-z must eventually compete with already-approved chronic therapies, including RNA-interference drugs from Alnylam Pharmaceuticals and stabilizer drugs such as tafamidis from Pfizer and acoramidis from BridgeBio. In hereditary angioedema, lonvo-z would enter a market with established prophylaxis options from companies such as Takeda and CSL. A one-time editing therapy must demonstrate a compelling advantage over these entrenched, repeat-dose treatments to gain adoption.
How to invest in Intellia Therapeutics, Inc. (NTLA)
There are three common ways to get NTLA exposure. Buy shares (or fractional shares) directly at any major broker. Hold an ETF that includes it (ARKG), which spreads the position across many companies. Or build it into a focused thematic basket, so NTLA sits alongside other stocks that express the same thesis.
Walnut takes the basket route. Describe a thesis where NTLA fits (for example “AI infrastructure” or “dividend-growth large-caps”) and the AI proposes 5 to 6 constituents with target weights. You review the plan and fund it through your own broker when you're ready.
The bottom line on Intellia Therapeutics, Inc. (NTLA)
Intellia Therapeutics is a pre-commercial gene-editing company whose value is concentrated in a small number of late-stage programs that have not yet reached the market. If you believe in vivo CRISPR editing will become a durable treatment modality and that lonvo-z and nex-z can clear regulatory review and launch successfully over the next few years, the relevant questions become position sizing and overlap with other speculative biotech holdings, not timing. The opposing case is that any single clinical setback, regulatory delay, or safety signal could sharply reduce the stock's value, and that continued cash burn means shareholders face ongoing dilution risk before the company ever earns a profit.
More on Intellia Therapeutics, Inc. (NTLA)
Whether NTLA is worth buying today depends more on your time horizon and what you already hold than on any single call. We walk through valuation, what would have to go right, and the risks in is NTLA a buy?, and where the stock could go from here in the NTLA stock forecast.
For income investors, whether NTLA pays a dividend and how the payout looks is covered in does NTLA pay a dividend?
Build a basket around NTLA with Walnut
Use Intellia Therapeutics, Inc. as one constituent in a thematic basket Walnut's AI helps you assemble. Describe a thesis you believe in, the AI proposes the holdings and weights, and you approve before any broker order.
FAQ
What does Intellia do?
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Intellia Therapeutics is a clinical-stage biotechnology company that develops genome-editing medicines using CRISPR/Cas9. Its specialty is in vivo editing, delivering the editing machinery directly into the body so a single dose can permanently alter a disease-causing gene. Its two lead programs are lonvo-z for hereditary angioedema and nex-z for ATTR amyloidosis, the latter partnered with Regeneron Pharmaceuticals.
Is NTLA a good stock to buy right now?
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That depends entirely on an investor's risk tolerance and time horizon, and this is not advice. The bull case is positive Phase 3 lonvo-z data, an active FDA filing, a Regeneron-partnered ATTR program, and a validated in vivo platform. The bear case is that NTLA is pre-revenue, unprofitable, burns roughly $90 to $100 million per quarter, and depends on binary trial and regulatory outcomes that can move the stock sharply.
Is NTLA profitable?
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No. Intellia is a clinical-stage, pre-revenue company that records only collaboration revenue and has no approved products generating sales. It reported a net loss of roughly $96 million in the first quarter of 2026 and funds operations through cash reserves and periodic equity raises. Profitability would depend on successfully bringing lonvo-z, nex-z, or another program to market, which has not yet happened.
Does NTLA pay a dividend?
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No. Intellia Therapeutics does not pay a dividend. As an unprofitable, pre-commercial biotech, the company directs all of its capital toward clinical development and operations rather than returning cash to shareholders. Investors seeking dividend income would need to look elsewhere in the healthcare or broader market, as any return from NTLA would have to come from share-price appreciation.
What is the difference between lonvo-z and nex-z?
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Both are in vivo CRISPR therapies but target different diseases. Lonvo-z (formerly NTLA-2002) is for hereditary angioedema and is wholly described by Intellia; it reported positive Phase 3 HAELO results and entered FDA filing in 2026. Nex-z (formerly NTLA-2001) targets ATTR amyloidosis, is developed with Regeneron, and is in the Phase 3 MAGNITUDE and MAGNITUDE-2 trials after the FDA lifted earlier clinical holds.
How much cash does Intellia have and what is its runway?
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Intellia reported approximately $517 million in cash, cash equivalents, and marketable securities as of March 31, 2026, and an April 2026 equity offering added roughly $207 million in gross proceeds. Management has stated this is expected to fund operations at least into 2028. Because the company burns roughly $90 to $100 million per quarter, additional capital raises before reaching profitability remain likely.
Who are Intellia's main competitors?
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The closest pure-play peers are CRISPR Therapeutics (CRSP), which has an approved CRISPR product, and Editas Medicine (EDIT). Beam Therapeutics (BEAM) competes with base editing. In Intellia's target diseases, nex-z would face approved ATTR therapies from Alnylam, Pfizer, and BridgeBio, while lonvo-z would face established hereditary angioedema prophylaxis from companies such as Takeda and CSL.
What is the biggest risk of investing in NTLA?
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The biggest risk is the binary, pre-revenue nature of the business. Intellia's value is concentrated in a few late-stage programs, so a failed trial, safety signal, or regulatory delay for lonvo-z or nex-z could sharply reduce the stock. The company is also unprofitable and burns cash, meaning shareholders face ongoing dilution risk from future equity raises before any product ever turns a profit.
Walnut is informational, not investment advice. Financial figures on this page are approximations; always verify current numbers with Intellia Therapeutics, Inc.'s investor relations page or your broker before making investment decisions.