Editas Medicine
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Editas Medicine

http://www.editasmedicine.com/
Last activity: 03.10.2024
Active
Categories: BioTechBodyCareCauseCultureDevelopmentHealthTechTechnology
What if you could repair broken genes? That is the question we ask ourselves every day at Editas Medicine. We’re a leading genome editing company focused on translating the power and promise of our proprietary genome editing systems into medicines to help transform the lives of people with genetically-defined diseases. Our goal is to discover, develop, manufacture, and commercialize transformative medicines for a range of serious diseases, including eye diseases, blood diseases, and cancer.

We are a vibrant company full of hope, possibilities, and a belief that, working together as One Editas, we can truly revolutionize the development of medicines. We are on an important journey to unlock the full potential of genome editing technology. A journey fueled by our distinct culture, expert team of Editas Medicine ‘Editors’, and the patients we aspire to help around the world. Connect with us to hear about the tremendous progress and scientific advancements we’ve already made and the next breakthrough on the horizon. If you are ingenious, passionate and resilient, come join the revolution. Repairing broken genes is only the beginning.
Website visits
24K /mo.
Mentions
62
Location: United States, Massachusetts, Cambridge
Employees: 201-500
Total raised: $120M
Founded date: 2013

Investors 5

Funding Rounds 1

DateSeriesAmountInvestors
10.08.2015Series B$120MGV

Mentions in press and media 62

DateTitleDescription
03.10.2024Editas Medicine Announces $50+ Million Monetization Financing with DRI Healthcare TrustCAMBRIDGE, Mass., Oct. 03, 2024 (GLOBE NEWSWIRE) -- Editas Medicine, Inc. (Nasdaq: EDIT), a clinical-stage gene editing company, today announced the sale of certain future license fees and other payments owed to Editas Medicine under its Ca...
14.05.2024CRISPR на практике. Восстанавливая зрениеБуквально на днях публиковал новость о том, что в мир вышла нейросеть, которая предлагает немалый потенциал для развития биотехнологий. И что возможности современной медицины постепенно расширяются. Что ж, мир технологий и правда не стоит н...
06.05.2024CRISPR Gene Editing Shows Promise: Early Trial Improves Vision in Blind ChildrenQuincy Jon, Tech Times 06 May 2024, 07:05 pm An early-stage clinical experiment published in the New England Journal of Medicine found that gene therapy can improve hereditary blindness. Researchers from the Children's Hospital of Philadelp...
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...
08.03.2024CRISPR Technology Takes Center Stage at SXSW 2024 for the First Time-
11.02.2022With sotrovimab in the balance, Biogen vet reunites with George Scangos at Vir; First woman to chair PhRMA has more in store at TakedaJohanna Friedl-Naderer Vir Biotechnology is getting another Biogen vet to join up as the startup’s new global CBO and EVP. While Johanna Friedl-Naderer officially doesn’t start her first C-suite role for another few weeks on March 2, she wi...
29.09.2021Editas Medicine : Review of BRILLIANCE Phase 1/2 Single Ascending Dose Study of EDIT-101 PresentationBRILLIANCE: A Phase 1/2 Single Ascending Dose Study of EDIT-101, an in vivo CRISPR Gene Editing Therapy in CEP290-Related Retinal Degeneration September 29, 2021 Forward Looking Statements This presentation contains forward-looking statemen...
07.10.2020‘A terrific choice’: George Church salutes fellow CRISPR pioneers’ historic Nobel winGeorge Church, who is in the thick of both the science and the business of editing genomes with the now Nobel-Prize-winning technology called CRISPR, warmly greeted Wednesday’s award in chemistry to fellow pioneers Emmanuelle Charpentier an...
16.10.2019Amar­na rais­es €10M to push gene ther­a­py plat­form in­to clin­ic; Ed­i­tas Med­i­cine, AskBio join forces→ Amar­na Ther­a­peu­tics — de­vel­op­ing an SV40-based gene de­liv­ery vec­tor plat­form called SVac — has raised €10 mil­lion. The round was led by Swedish in­vest­ment com­pa­ny Flerie In­vest AB, along with con­tri­bu­tions from the Net...
26.07.2019Editas, Allergan open first trial of in vivo CRISPR therapyLast month, Chicago-based AbbVie said it would acquire Allergan – best known for manufacturing drugs like Botox (onabotulinumtoxinA) – for $63 billion. LCA10 is caused by mutations in the CEP290 gene and is one of several subtypes of LCA. L...
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