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Intellia Therapeutics develops CRISPR-Cas9 genome editing therapies to treat severe genetic diseases. Its work centers on using CRISPR to edit genes and delivering the editing tools to the right cells with a modular lipid nanoparticle system, aiming to create treatments that can be given to patients and move through clinical trials toward market. The company earns revenue through R&D collaborations, licensing, and potential sales of approved therapies. Compared to others in biotech, Intellia emphasizes in vivo gene editing using a distinctive lipid nanoparticle delivery approach and active partnerships to advance candidates. Its goal is to bring safe, effective genome-editing treatments to patients while building value through collaborations and licensing.
Industries
Biotechnology
Healthcare
Company Size
501-1,000
Company Stage
IPO
Headquarters
Cambridge, Massachusetts
Founded
2014
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Total Funding
$1.8B
Above
Industry Average
Funded Over
10 Rounds
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CRISPR Therapeutics outlook: scaling gene editing by 2036. Key takeaways. * CRISPR Therapeutics currently reports $10.2 million in quarterly revenue against a $91.2 million net loss, highlighting the heavy R&D burden of its current pipeline. * The company is pivoting from ex-vivo therapies like Casgevy toward in-vivo editing, which could expand its addressable patient population from 150,000 to 400,000. * By 2036, the success of SyNTase editing and in-vivo delivery methods will determine if the firm transitions from a niche biotech to a diversified genomic medicine powerhouse. TrendPulse analysis. Industry context. The gene-editing landscape is moving beyond the "proof of concept" phase into a period of rigorous commercial validation. Historically, the sector has been defined by high-cost, one-time curative treatments. However, the industry is now facing a "delivery bottleneck." Competitors like **Intellia Therapeutics** and **Beam Therapeutics** are also racing to solve the in-vivo delivery challenge, as the market increasingly favors standardized, off-the-shelf products over the bespoke, patient-specific manufacturing processes that currently dominate the space. Furthermore, the regulatory environment is becoming more sophisticated. As seen with recent setbacks at major pharmaceutical firms like **Novartis**, regulators are no longer satisfied with biomarker improvements alone. They now demand clear, long-term clinical outcomes that translate into tangible patient health benefits. This shift forces companies like CRISPR Therapeutics to prove not just that they can edit a gene, but that the edit reliably prevents disease progression in real-world settings. The industry is effectively moving from a "technology-first" mindset to a "clinical-outcome-first" mandate. Why this matters. For investors and industry stakeholders, the next decade represents a transition from speculative growth to operational maturity. The primary risk is no longer just scientific failure, but commercial viability. If CRISPR Therapeutics successfully transitions to in-vivo delivery, it will fundamentally change the economics of the business, moving from a high-cost service model to a scalable product model. This would likely trigger a wave of M&A activity, as large-cap pharmaceutical companies look to acquire proven, scalable genomic platforms to replenish their aging pipelines. However, the path to 2036 is fraught with "clinical disconnect" risks - where the editing works, but the patient outcome does not improve as expected. Decision-makers should monitor the company's ability to manage its cash burn while navigating these long-term trials. The winners in this space will be those who can balance the high costs of R&D with a clear, cost-effective path to commercialization. Investors should look for evidence of manufacturing efficiency and partnerships that can handle the global distribution of these complex therapies once they reach the market. The bottom line. CRISPR Therapeutics' long-term value hinges on its ability to transition from complex, ex-vivo procedures to scalable in-vivo therapies that deliver measurable, long-term clinical outcomes. Read the full article. This analysis is based on reporting from nasdaq Finance AI-powered news analysis · September 18, 2026 Editorially Reviewed
Intellia Therapeutics' (NTLA) market outperform rating reiterated at Citizens Jmp. September 9, 2026 Key points. * Citizens JMP reiterated its "Market Outperform" rating on Intellia Therapeutics and maintained a $30 price target, implying approximately 135% upside from the reported $12.74 share price. * Analyst sentiment remains mixed: Intellia has an average rating of "Hold" and an average price target of $20.98, despite recent "Outperform" and "Buy" upgrades or reiterations from several firms. * Intellia reported a quarterly loss of $0.80 per share, in line with estimates, but revenue of $7.66 million fell short of the $12.98 million consensus and declined 46.4% year over year. * MarketBeat previews top five stocks to own in October. Intellia Therapeutics (NASDAQ:NTLA - Get Free Report)'s stock had its "market outperform" rating reissued by investment analysts at Citizens Jmp in a report issued on Wednesday, Benzinga reports. They presently have a $30.00 price objective on the stock. Citizens Jmp's price target points to a potential upside of 135.48% from the stock's current price. NTLA has been the topic of several other research reports. Evercore raised Intellia Therapeutics from a "hold" rating to an "outperform" rating and set a $24.00 price objective on the stock in a research note on Friday, August 7th. HC Wainwright restated a "buy" rating and issued a $25.00 price objective on shares of Intellia Therapeutics in a report on Wednesday. Sanford C. Bernstein increased their target price on shares of Intellia Therapeutics from $13.00 to $17.00 and gave the stock a "market perform" rating in a report on Wednesday, May 13th. Wedbush lifted their price objective on shares of Intellia Therapeutics from $12.00 to $13.00 and gave the company a "neutral" rating in a report on Wednesday. Finally, Citigroup restated a "market outperform" rating on shares of Intellia Therapeutics in a report on Tuesday, August 25th. One analyst has rated the stock with a Strong Buy rating, ten have issued a Buy rating, eight have assigned a Hold rating and four have given a Sell rating to the stock. According to data from MarketBeat, the stock presently has an average rating of "Hold" and an average target price of $20.98. Intellia Therapeutics stock performance. NASDAQ:NTLA opened at $12.74 on Wednesday. The stock has a fifty day simple moving average of $12.78 and a 200-day simple moving average of $13.42. The company has a market cap of $1.79 billion, a price-to-earnings ratio of -3.79 and a beta of 1.82. Intellia Therapeutics has a twelve month low of $7.95 and a twelve month high of $28.25. Discover more Get Business Reports Cryptocurrency market data Intellia Therapeutics (NASDAQ:NTLA - Get Free Report) last announced its quarterly earnings data on Thursday, August 6th. The company reported ($0.80) earnings per share for the quarter, meeting analysts' consensus estimates of ($0.80). The company had revenue of $7.66 million during the quarter, compared to analyst estimates of $12.98 million. Intellia Therapeutics had a negative net margin of 672.16% and a negative return on equity of 57.79%. The firm's revenue for the quarter was down 46.4% on a year-over-year basis. During the same quarter last year, the business posted ($0.98) EPS. As a group, equities research analysts predict that Intellia Therapeutics will post -3.21 EPS for the current fiscal year. Insider activity. In other news, EVP Edward J. Dulac III sold 4,677 shares of the company's stock in a transaction dated Thursday, July 2nd. The stock was sold at an average price of $18.00, for a total value of $84,186.00. Following the sale, the executive vice president owned 156,286 shares in the company, valued at $2,813,148. This represents a 2.91% decrease in their ownership of the stock. The sale was disclosed in a filing with the Securities & Exchange Commission, which is available through the SEC website. Also, CAO Michael P. Dube sold 2,641 shares of the firm's stock in a transaction dated Wednesday, July 1st. The shares were sold at an average price of $16.78, for a total value of $44,315.98. Following the sale, the chief accounting officer owned 66,886 shares in the company, valued at $1,122,347.08. This trade represents a 3.80% decrease in their ownership of the stock. Additional details regarding this sale are available in the official SEC disclosure. The sale was made to cover tax withholding obligations related to the vesting of equity awards. 3.50% of the stock is currently owned by insiders. Hedge funds weigh in on Intellia Therapeutics. Several hedge funds and other institutional investors have recently made changes to their positions in NTLA. BlackRock Inc. acquired a new stake in Intellia Therapeutics during the 2nd quarter worth $260,721,000. ARK Investment Management LLC lifted its holdings in Intellia Therapeutics by 19.2% in the fourth quarter. ARK Investment Management LLC now owns 14,207,324 shares of the company's stock valued at $127,724,000 after acquiring an additional 2,288,146 shares during the last quarter. Vanguard Group Inc. grew its position in Intellia Therapeutics by 17.8% in the fourth quarter. Vanguard Group Inc. now owns 13,010,001 shares of the company's stock worth $116,960,000 after acquiring an additional 1,965,181 shares during the period. State Street Corp raised its position in Intellia Therapeutics by 29.1% in the fourth quarter. State Street Corp now owns 6,418,836 shares of the company's stock valued at $57,705,000 after purchasing an additional 1,447,967 shares during the period. Finally, Geode Capital Management LLC grew its holdings in shares of Intellia Therapeutics by 4.1% during the 4th quarter. Geode Capital Management LLC now owns 2,696,187 shares of the company's stock worth $24,243,000 after purchasing an additional 107,333 shares during the period. Hedge funds and other institutional investors own 88.77% of the company's stock. Intellia Therapeutics news roundup. Here are the key news stories impacting Intellia Therapeutics this week: * The FDA granted Priority Review to Intellia's biologics license application for lonvo-z and set a PDUFA decision date of March 10, 2027. If approved, lonvo-z could become the first in vivo CRISPR-based therapy and the only one-time treatment for HAE, offering substantial commercial differentiation. * HC Wainwright reaffirmed its Buy rating and assigned a $25 price target, implying substantial potential upside from the stock's recent $12.74 level. The target reflects optimism about lonvo-z and Intellia's CRISPR platform. * Wedbush raised its price target to $13 from $12 but maintained a Neutral rating. The revised target indicates only limited near-term valuation upside and shows that analysts remain cautious despite the FDA milestone. * Intellia was highlighted among genomics companies attracting investor interest in 2026, reinforcing broader enthusiasm for gene-editing and precision-medicine technologies, but the article did not announce a new company-specific development. About Intellia Therapeutics. Intellia Therapeutics, Inc NASDAQ: NTLA is a clinical-stage biotechnology company focused on developing potentially curative genome editing therapies using the CRISPR/Cas9 platform. The company's research spans both in vivo and ex vivo applications of CRISPR/Cas9, aiming to correct or disable disease-causing genes with a single administration. Intellia's lead in vivo program targets transthyretin amyloidosis (ATTR) by delivering CRISPR/Cas9 machinery directly to the liver, while additional preclinical efforts pursue treatments for hemophilia A, hereditary angioedema and other genetic disorders. Beyond its in vivo pipeline, Intellia collaborates with strategic partners to extend the impact of its genome editing approach. This instant news alert was generated by narrative science technology and financial data from MarketBeat in order to provide readers with the fastest reporting and unbiased coverage. Please send any questions or comments about this story to [email protected]. Before you consider Intellia Therapeutics, you'll want to hear this. MarketBeat keeps track of Wall Street's top-rated and best performing research analysts and the stocks they recommend to their clients on a daily basis. MarketBeat has identified the five stocks that top analysts are quietly whispering to their clients to buy now before the broader market catches on... and Intellia Therapeutics wasn't on the list. While Intellia Therapeutics currently has a Hold rating among analysts, top-rated analysts believe these five stocks are better buys. Enter your email address and we'll send you MarketBeat's list of ten stocks set to soar in Fall 2026, despite the threat of tariffs and what's happening in Iran. These ten stocks are incredibly resilient and are likely to thrive in any economic environment. Continue following MarketBeat
Intellia Therapeutics, Inc. secures non-dilutive debt facility with OrbiMed for up to $400 million. Published on 09/04/2026 at 12:06 pm EDT S&P Capital IQ Intellia Therapeutics, Inc. announced that it has entered into a $400 million non-dilutive senior secured term loan facility with OrbiMed, a leading global healthcare investment firm. The facility includes an initial term loan of $75 million that was funded at closing; 5 additional tranches totaling up to $225 million that can be drawn at Intellia?s option subject to its achievement of specified milestones related primarily to lonvo-z; and an additional $100 million available subject to mutual agreement between the parties during the five-year term of the agreement. Additional details of the loan agreement will be filed with the Securities and Exchange Commission on a Current Report on Form 8-K. TD Cowen acted as exclusive financial advisor to Intellia on the transaction. Goodwin Procter LLP acted as legal advisor to Intellia. Covington & Burling LLP acted as legal advisor to OrbiMed. (C) S&P Capital IQ - 2026
Intellia Therapeutics has secured a $400 million non-dilutive senior secured term loan facility with OrbiMed. The deal includes an initial $75 million funded at closing, with up to $225 million available in additional tranches subject to achieving milestones related to lonvoguran ziclumeran (lonvo-z), its treatment for hereditary angioedema. Another $100 million may be available by mutual agreement during the five-year term. The financing provides Intellia with financial flexibility as it prepares for a planned US approval and commercial launch of lonvo-z. "This non-dilutive financing enables us to more freely execute our plan to successfully launch lonvo-z in HAE, advance nexiguran ziclumeran through multiple important milestones in transthyretin amyloidosis and create value through our early pipeline development efforts," said Edward Dulac, Intellia's chief financial officer. TD Cowen acted as exclusive financial adviser to Intellia on the transaction.
6 companies hiring in Cambridge now. July 22, 2026 | Looking for a biopharma job in Cambridge? Roles posted on BioSpace have more than doubled compared to last year. Life sciences professionals looking for employment in Cambridge, Massachusetts, may find more opportunities in that part of the Genetown Hotbed now than they did a year ago. Job postings live on the BioSpace website for Cambridge jumped 120% year over year. They started trending up in February, with only a slight dip in May before rising again last month. If you're interested in working at a pharma or biotech in Cambridge, check out the open positions at these six companies. * Intellia Therapeutics has around 40 jobs available. Roles include vice president, gene editing core; senior director, quality management systems and compliance; and manager, commercial systems. * Regeneron has about a dozen openings. Jobs include scientist-analytical development, Regeneron cell medicines; senior toxicologist; and senior manager clinical study lead (clinical experimental sciences). * Sanofi has over 100 roles available. Positions include senior associate scientist; clinical research director; and director, commercial transformation. * AbbVie has several openings. Jobs include associate scientist, cellular/molecular biochemistry II; senior scientist II, rheumatology; and senior principal scientist, immune cell depletion discovery group, immunology discovery research. * Amgen also has several positions available. Roles include senior quality engineer; process development senior scientist-pivotal drug product technologies; and device engineering senior engineer. * Moderna has over 50 openings. Jobs include scientist, oncology bioinformatics; manager, biomarker operations; and senior research associate, in vivo pharm. Job market trends, layoffs and career advice to manage your life sciences career Angela Gabriel is content manager, life sciences careers, at BioSpace. She covers the biopharma job market, job trends and career advice, and produces client content. You can reach her at [email protected] and follow her on LinkedIn.
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Industries
Biotechnology
Healthcare
Company Size
501-1,000
Company Stage
IPO
Headquarters
Cambridge, Massachusetts
Founded
2014
Find jobs on Simplify and start your career today