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Intellia Therapeutics, Inc. (NTLA)

NasdaqGM - NasdaqGM Real Time Price. Currency in USD
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Previous Close63.57
Bid0.00 x 800
Ask0.00 x 1100
Day's Range59.80 - 65.28
52 Week Range9.18 - 92.00
Avg. Volume1,743,010
Market Cap4.116B
Beta (5Y Monthly)2.05
PE Ratio (TTM)N/A
EPS (TTM)-2.27
Earnings DateFeb 25, 2021
Forward Dividend & YieldN/A (N/A)
Ex-Dividend DateN/A
1y Target Est74.58
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  • Intellia Therapeutics to Hold Conference Call to Discuss Fourth Quarter and Full-Year 2020 Earnings and Company Updates

    Intellia Therapeutics to Hold Conference Call to Discuss Fourth Quarter and Full-Year 2020 Earnings and Company Updates

    CAMBRIDGE, Mass., Feb. 18, 2021 (GLOBE NEWSWIRE) -- Intellia Therapeutics, Inc. (NASDAQ:NTLA), a leading genome editing company focused on developing curative therapeutics using CRISPR/Cas9 technology both in vivo and ex vivo, will present its fourth quarter and full-year 2020 financial results and operational highlights in a conference call on February 25, 2021 at 8 a.m. ET. To join the call: U.S. callers should dial 1-833-316-0545 and international callers should dial 1-412-317-5726, approximately five minutes before the call.All participants should ask to be connected to the Intellia Therapeutics conference call. A replay of the call will be available through the Events and Presentations page of the Investors & Media section of the company’s website at www.intelliatx.com, beginning on February 25, 2021 at 12 p.m. ET. About Intellia TherapeuticsIntellia Therapeutics is a leading genome editing company, focused on the development of proprietary, potentially curative therapeutics using the CRISPR/Cas9 system. Intellia believes the CRISPR/Cas9 technology has the potential to transform medicine by both producing therapeutics that permanently edit and/or correct disease-associated genes in the human body with a single treatment course, and creating enhanced engineered cells that can treat oncological and immunological diseases. Intellia’s combination of deep scientific, technical and clinical development experience, along with its leading intellectual property portfolio, puts it in a unique position to unlock broad therapeutic applications of the CRISPR/Cas9 technology and create new classes of therapeutic products. Learn more about Intellia and CRISPR/Cas9 at intelliatx.com. Follow us on Twitter @intelliatweets. Intellia Contacts: Investors:Glenn GoddardChief Financial Officer+1-857-706-1056glenn.goddard@intelliatx.com Media:Julie FergusonInterim Head of External Affairs & Communications+1-312-385-0098julie.ferguson@intelliatx.com

  • InvestorPlace

    A Highly Specialized Gene Editing Stock with a Clear Pathway to Big Gains

    Welcome to the Genomic Revolution. It’s been a long, long journey… but we are finally at the point where genomics – the branch of molecular biology concerned with the structure, function, evolution, and mapping of genomes – is ready to change the world. DNA was first identified back in the 1860s by Swiss chemist Friedrich Miescher. In 1953, James Watson and Francis Crick discovered the double helix structure of DNA. 24 years later, Frederick Sanger developed the world’s first DNA sequencing technique to determine the order of nucleotides in DNA.InvestorPlace - Stock Market News, Stock Advice & Trading Tips Over the course of the next three decades, researchers proceeded to map the human genome. Then, in 2012, Jennifer Doudna and Emmanuelle Charpentier changed the world when they created a novel gene editing technique – dubbed CRISPR-Cas9 – that could be used to modify the human genome. And now… artificial intelligence is converging with decades of breakthrough genomics research to create a new generation of hyper-efficient, hyper-accurate, and hyper-precise gene editing medicines. Those medicines are going through clinical trials today. The first will likely be in-market within the next few years. In other words, the 160-year-old dream of gene editing is finally turning into a reality. That’s a big deal. Gene editing – at scale – has the potential to cure disease, fix genetic disorders, improve food quality, alleviate resource depletion, and so much more. Gene editing will, quite literally, change everything… because, after all, it enables us to change DNA, and every living thing in this world is built on DNA. It goes without saying, then, that this is the breakthrough of a century. And – considering it’ll all turn into a reality within the next few years – the time to invest in the Genomic Revolution is today. Today, we will give you one way to play this once-in-a-lifetime revolution. It’s by buying a highly specialized gene editor that has a clear pathway to unlocking huge gains throughout the 2020s by curing genetic disorders no one else is targeting. The Genomic Biotech Leader in Relatively Niche & Competition-less Markets As longtime readers know, there are only a handful of large, well-established gene editors with robust and mature therapy pipelines in the world today. Because gene editing science is somewhat homogenous, many of them are attacking the same end-markets, like ocular diseases and sickle cell disease. But not Intellia Therapeutics (NTLA). Founded by Jennifer Doudna – widely considered the “Mother of CRISPR-Cas9” – this $5 billion gene editor is as mature and well-established as anyone in the genomics industry, with one gene-edited medicine that is already in Phase 1 clinical trials. But, importantly, Intellia is not attacking the crowded ocular and sickle cell disease markets. Instead, Intellia is targeting smaller, more specialized markets with its portfolio of therapies. The first such market? Transthyretin amyloidosis (ATTR), a progressive condition caused by a buildup of abnormal deposits of protein in the body’s organs and tissues, and which negatively impacts nerves, the heart, kidneys, and the eyes. It’s a fairly rare condition (less than 600,000 patients globally), with a small addressable market (the treatment market today measures under $1 billion), but Intellia is the undisputed leader in pioneering a gene-edited medicine to entirely eradicate ATTR with its NTLA-2001 medicine that is in Phase 1 clinical trials. Meanwhile, the company’s two other leading medicines – NTLA-2002 and NTLA-5001 – are also attacking niche markets. NTLA-2002 is targeted at curing hereditary angioedema (HAE), a genetic disorder characterized by consistent and severe swelling. It, too, is the leading gene-edited medicine in its target market. NTLA-5001, meanwhile, is targeted at curing Acute Myeloid Leukemia (AML) – and, as you probably guessed, is also the leading gene-edited therapy for AML. Intellia expects to submit INDs for both medicines in 2021. Thus, by early 2022, Intellia could have three leading gene-edited medicines going through clinical trials. If all three medicines pass clinical trials – which looks plausible given robust early clinical data – then Intellia will have three very potent, approved gene-edited medicines in largely competition-less markets by the mid-2020s. Does that sound like a winning recipe? It should. Alone, Intellia’s niche medicines don’t pack a big punch. But, when bundled together, they do pack a big bunch. Between the HAE, AML, and ATTR end-markets, Intellia’s addressable market should measure ~$20 billion by the end of the decade. Intellia should be able to capture a big chunk of that market, meaning that this is easily a $5+ billion company in the long run. Biotech stocks typically trade around 8X sales. That typical multiple implies a potential future valuation for this specialized gene editor of at least $40 billion. That, of course, is large enough upside to warrant putting Intellia Therapeutics stock on your buy radar today. On the date of publication, Luke Lango did not have (either directly or indirectly) any positions in the securities mentioned in this article. The New Daily 10X Stock Report: 98.7% Accuracy — Gains Up to 466.78%. InvestorPlace’s brand-new and highly controversial newsletter… is rocking the industry… delivering one breakthrough stock recommendation each and every trading day… delivered straight to your inbox. 98.7% Accuracy to Date — Gains Up to 466.78%. Now for a limited time… you can get in for just $19. Click here to find out how.The post A Highly Specialized Gene Editing Stock with a Clear Pathway to Big Gains appeared first on InvestorPlace.

  • The Zacks Analyst Blog Highlights: CRISPR Therapeutics, Vertex Pharmaceuticals and Intellia Therapeutics

    The Zacks Analyst Blog Highlights: CRISPR Therapeutics, Vertex Pharmaceuticals and Intellia Therapeutics

    The Zacks Analyst Blog Highlights: CRISPR Therapeutics, Vertex Pharmaceuticals and Intellia Therapeutics