CRISPR Therapeutics
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CRISPR Therapeutics

http://crisprtx.com/
Last activity: 07.08.2026
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Categories: BioTechBusinessHealthTechHumanMedtechPlatformPublicTechnology
CRISPR Therapeutics is a leading gene editing company focused on developing transformative gene-based medicines for serious diseases using its proprietary CRISPR/Cas9 platform. CRISPR/Cas9 is a revolutionary gene editing technology that allows for precise, directed changes to genomic DNA. CRISPR Therapeutics has established a portfolio of therapeutic programs across a broad range of disease areas including hemoglobinopathies, oncology, regenerative medicine and rare diseases. To accelerate and expand its efforts, CRISPR Therapeutics has established strategic collaborations with leading companies including Bayer, Vertex Pharmaceuticals and ViaCyte, Inc. CRISPR Therapeutics AG is headquartered in Zug, Switzerland, with its wholly-owned U.S. subsidiary, CRISPR Therapeutics, Inc., and R&D operations based in Cambridge, Massachusetts, and business offices in San Francisco, California and London, United Kingdom.
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Location: United States, Massachusetts, Cambridge
Employees: 201-500
Total raised: $127M
Founded date: 2013

Investors 8

Funding Rounds 3

DateSeriesAmountInvestors
27.06.2016Series B$38MNew Leaf V...
30.04.2015Series A$64M-
24.04.2014Series A$25M-

Mentions in press and media 83

DateTitleDescription
07.08.2026Three Swiss biotechs widen their reach into pharma, paediatrics and lung disease SOPHiA GENETICS, a Rolle (VD)-based genomics company founded in 2011, runs SOPHiA DDM, a cloud platform that analyses genomic and multimodal data for hospitals, laboratories and biopharma partners. The company reported second-quarter reven...
04.07.2026CRISPR Sickle Cell Therapy Now Cleared for Children Starting at Age TwoBy Shannon Harwood Published: Jul 04 2026, 11:24 AM EDT Share on Facebook Share on Twitter Share on LinkedIn Share on Reddit Share on Flipboard
23.06.2026«Р-Фарм» вложился в терапию гепатита В методом редактирования генома«Р-Фарм» вложился в терапию гепатита В методом редактирования генома Технологию на основе CRISPR изначально разрабатывал Сеченовский университет «Р-Фарм» инвестировал в разработку Сеченовского университета на основе «молекулярных ножниц» — ...
23.02.2026FDA proposes new system for approving customized drugs and therapies for rare diseasesGetting your Trinity Audio player ready... By MATTHEW PERRONE, AP Health Writer WASHINGTON (AP) — Federal health officials on Monday laid out a proposal to spur development of customized treatments for patients with hard-to-treat diseases, ...
07.07.2025Swiss Innovators celebrated worldwide Quantum startup ZuriQ is among the winners of the Hamamatsu bi-annual Photonics Innovation Awards 2025 that was held during the award ceremony at Laser World of Photonics, the world’s leading photonics trade fair held in Munich, Germany. A...
28.05.2025These biotech stocks will benefit as generative AI speeds up drug discovery, Jefferies says-
15.04.2025Назад, в генетическое будущее-
11.02.2025Vertex forecasts upbeat 2025 revenue on cystic fibrosis treatments demandVertex forecasts upbeat 2025 revenue on cystic fibrosis treatments demand By ReutersFebruary 10, 20259:13 PM UTCUpdated ago Text Small Text Medium Text Large Text Share X Facebook Linkedin Email Link A sign hangs in front of the world headq...
15.01.2025The Race for AI: Innovation and Impending DoomIn the world of artificial intelligence, innovation races ahead like a speeding train. Researchers from AIRI, along with their international partners, have made headlines by reaching the finals of the prestigious Concordia Challenge. This c...
14.01.2025Нейросети, робототехника и апокалипсисКак повлияет развитие нейросетей и робототехники на рынок труда? Появится ли в ближайшие годы настоящий сильный ИИ? Если сильный ИИ появится - захочет ли он уничтожить человечество? Не используют ли власти большинства стран нейросети, ИИ и ...
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