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Intellia Therapeutics
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Intellia Therapeutics

https://www.intelliatx.com/?portfolioCats=34,23,29,35,22,24,30,25,28,31#new_tab
Last activity: 30.03.2026
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Categories: BioTechBodyDevelopmentHealthTechHumanIndustryProductPropertyTechnologyTools
Intellia Therapeutics is a leading genome editing company whose mission is to develop potentially curative gene editing treatments that can positively transform the lives of people living with severe and life-threatening diseases. We are focused on the development of proprietary therapeutics using a recently developed biological tool known as the CRISPR/Cas9 system. The promise of the CRISPR/Cas9 system is the driving force behind the creation of Intellia. Our founders have a shared belief that the CRISPR/Cas9 technology has the potential to transform medicine by permanently editing disease-associated genes in the human body with a single treatment course. This technology offers the potential for us to develop curative therapeutic options for patients with chronic diseases by addressing the underlying cause of the disease. It can bring new hope and cures to people who now have nowhere to turn for help. Our combination of deep scientific expertise and clinical development experience, along with our leading intellectual property portfolio, puts Intellia in a unique position to unlock broad therapeutic applications of the CRISPR/Cas9 technology and create a new class of therapeutic products. Intellia has the right people, assets and ambitious vision needed to take full advantage of the CRISPR/Cas9 technology’s attributes – high potency, specificity, simplicity of use, broad applicability, and multifunctional programmability – and accelerate the advancement of curative products into the clinic. View our social media community guidelines at https://www.intelliatx.com/terms-and-conditions/ .
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Website visits
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Mentions
56
Location: United States, Massachusetts, Cambridge
Employees: 201-500
Total raised: $85M
Founded date: 2014

Investors 7

Funding Rounds 2

DateSeriesAmountInvestors
01.09.2015Series B$70M-
19.11.2014Series A$15M-

Mentions in press and media 56

DateTitleDescription
30.03.2026We’re exiting this tech stock to replenish our cash pile after our annual charity donation-
20.02.2026Curt Smith: Fighting blood cancer is easier with a group effort-
26.10.2025S&P 500 rallies 1% to notch first close ever above 6,800 on potential China trade truce: Live updatesStocks jumped to new records on Monday after U.S. and China officials cooled tensions over the weekend, laying the groundwork for President Donald Trump and China President Xi Jinping to clinch a trade deal this week. The S&P 500 climbe...
13.06.2025Signify Bio: $15 Million Raised For Creating Personalized MedicinesSignify Bio, which is a pioneering biotechnology company harnessing the human body for the production of in situ protein therapeutics, announced an oversubscribed $15 million initial financing. The funding round was led by Actium Group with...
15.04.2025Назад, в генетическое будущее-
31.03.2025Epicrispr Biotechnologies: A New Dawn in Genetic TherapyEpicrispr Biotechnologies is making waves in the biotechnology sector. The company recently secured $68 million in Series B funding. This financial boost is a beacon of hope for patients suffering from facioscapulohumeral muscular dystrophy...
26.03.2025Epicrispr Biotechnologies Raises $68M in Series B FundingEpicrispr Biotechnologies, a South San Francisco, CA-based biotechnology company focused on developing curative therapies, raised $68m in the first close of its Series B financing. The round was led by Ally Bridge Group, with participation ...
11.11.20243 Fast-Growing Stocks Analysts See Doubling in Price Clinical-stage biotech firms often have massive upside potential, but much of that possible success hinges on successful trials and product launche... Comparing and selecting stocks for investment may involve any number of increasingly complex strategies and approaches, but sometimes simpler is better: targeting a stock with significant upside potential at an opportune moment. Certainly,...
07.06.2024Gene editing's next big targetsfigcaption>span]:font-sans"> Gene editing's next chapter will be focused on tackling cancers and more common diseases, uncovering new details about aging and other fundamental aspects of biology and editing RNA, top scientists in...
01.04.2024Впервые в мире почку свиньи изменили генетически и пересадили человеку. Теперь их можно массово пересаживать...Хирурги из США провели человеку трансплантацию почки, полученной из генетически модифицированной свиньи. СМИ сообщают, что данная операция является прорывом в области ксенотрансплантации, когда органы, клетки или ткани пересаживаются из одн...
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