February 7, 2024
Scrip – Scribe Therapeutics is one of a new generation of CRISPR-based gene-editing companies, and believes its in vivo CRISPR X-Editing (XE) technology could be the most efficient yet.
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January 17, 2024
ASBMB Today – Outside of academia, companies including Scribe Therapeutics are also developing gene therapies for diseases such as sickle cell.
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December 21, 2023
Endpoints News – The California-based CRISPR biotech has tapped Aarif Khakoo as CSO and head of R&D, and appointed Maria Mirotsou as VP of discovery biology.
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December 8, 2023
ASBMB Today – Benjamin Oakes, CEO and cofounder of Scribe Therapeutics, said “The approval is just the tip of the iceberg. It’s a really beautiful proof of concept for what CRISPR genome editing can do. … The real vision and mission for the whole CRISPR field should be to create safer, more effective therapies that can be brought more broadly to patients.”
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October 11, 2023
BioPharma Dive – “Large pharma is recognizing that this has the potential to be the future of medicine,” said Benjamin Oakes, co-founder and CEO of Scribe Therapeutics, an early-stage CRISPR drug developer now working with Eli Lilly and Sanofi.
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October 6, 2023
San Francisco Business Times – Interview with Svetlana Lucas, one of the outstanding professionals in the 2023 class of Most Influential Women in Bay Area Business.
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July 20, 2023
The Wall Street Journal – Drugmakers are doubling down on deals with genome-editing startup Scribe Therapeutics, which could earn more than $2 billion through its newly expanded collaboration with Sanofi.
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July 18, 2023
Seeking Alpha – Sanofi is receiving an exclusive license for privately held Scribe Therapeutics’ CRISPR X-Editing genome editing technologies to develop in vivo therapies.
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July 18, 2023
BioWorld – Scribe Therapeutics Inc. has announced an expanded collaboration with Sanofi SA, under which Sanofi receives an exclusive license to use Scribe’s CRISPR X-Editing (XE) genome editing technologies for the development of in vivo therapies, including for sickle cell disease.
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July 17, 2023
STAT – Sanofi will license a new CRISPR enzyme from the startup Scribe Therapeutics in a bid to be the first to develop a safer, simpler, and more scalable cure for sickle cell disease.
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July 17, 2023
San Francisco Business Times – It is the second potential multibillion-dollar deal between Alameda’s Scribe Therapeutics Inc. and Sanofi (NASDAQ: SNY) around the East Bay company’s technologies to make precise edits to cells.
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July 17, 2023
Fierce Biotech – Less than a year since partnering up for the first time, Sanofi and Scribe are at it again, this time working together on new in vivo therapies in a deal that could see the Jennifer Doudna-founded biotech in line for over $1.2 billion.
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July 17, 2023
BioPharma Dive – Under the new deal, Sanofi gets to use Scribe’s CRISPR-based gene editing technology to develop in vivo therapies as well.
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July 17, 2023
Endpoints News – Sanofi has inked another collaboration with its CRISPR partner Scribe Therapeutics as the duo seeks to create a newer, safer approach to tackling sickle cell disease.
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July 17, 2023
Evaluate Vantage – The latest deal focuses on in vivo Crispr editing for sickle cell disease, and follows last year’s cancer collaboration.
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July 17, 2023
BioCentury –Scribe CEO Benjamin Oakes told BioCentury the next-generation nuclease company had been seeking a partner with non-viral, extra-hepatic delivery vectors, and found it in Sanofi, with which it was already collaborating on NK cell therapies for cancer.
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May 19, 2023
Bloomberg Technology – CRISPR pioneer Jennifer Doudna’s company Scribe Therapeutics inked a major deal with Prevail Therapeutics potentially worth $1.5 billion to create genetic medicines for neurological and neuromuscular diseases. Scribe CEO Ben Oakes joins Caroline Hyde for more.
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May 19, 2023
Evaluate Vantage – Lilly is the latest group, after Biogen and Sanofi, to collaborate on Scribe’s novel approach to Crispr editing.
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May 17, 2023
BioSpace – At the core of the research collaboration are Scribe’s proprietary X-editing (XE) technologies, which allow the company to develop in vivo treatments with three key attributes: deliverability, specificity and greater editing activity.
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May 17, 2023
Labiotech – The deal gives Prevail exclusive rights to Scribe Therapeutics’ CRISPR X-Editing (XE) technologies for the development of in vivo therapies directed to specified targets known to cause serious neurological and neuromuscular diseases.
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May 17, 2023
Pharmaceutical Technology – The deal will see the integration of Scribe’s new CRISPR by Design approach and Prevail’s expertise in developing genetic medicines for neurological disorders for specific genetic targets.
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May 16, 2023
BioWorld – Scribe Therapeutics Inc. is selling exclusive rights to its CRISPR-based technology to Prevail Therapeutics Inc. for a figure that could top $1.6 billion as the firms team up to develop genetic therapies for serious neurological and neuromuscular diseases.
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May 16, 2023
San Francisco Business Times – Calling it “CRISPR by Design,” Scribe says those tools allow cuts to be made in our bodies, rather than engineered outside the body and infused inside humans.
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May 16, 2023
BioPharma Dive – Scribe’s partnership with New York-based Prevail is its biggest deal yet. Attached to the deal is $1.5 billion in “biobucks,” payments to Scribe contingent on research under the collaboration hitting certain milestones.
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May 16, 2023
Seeking Alpha – Scribe Therapeutics is collaborating with Eli Lilly’s unit (NYSE:LLY) Prevail Therapeutics and granted rights to its CRISPR X-Editing (XE) technologies to develop in vivo therapies for neurological and neuromuscular diseases.
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May 16, 2023
Genetic Engineering & Biotechnology News – Through its subsidiary Prevail, Lilly is the third biopharma giant to partner with Scribe on developing CRISPR-based therapies.
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May 16, 2023
Fierce Biotech – Eli Lilly’s Prevail Therapeutics is jotting down up to $1.5 billion for Scribe Therapeutics in hopes of writing some new CRISPR-based genetic medicines for neurological and neuromuscular diseases into history.
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April 11, 2023
I am BIO Podcast – CRISPR has emerged as a powerful tool for altering DNA sequences with incredible precision, opening up new avenues of research into the treatment of disease. This episode features scientists working to push these gene editing tools to the next frontier.
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February 15, 2023
Nature Biotechnology – Sanofi also turned to Scribe Therapeutics’ CRISPR platform to develop off-the shelf NK cell therapies for oncology, paying $25 million up front in a deal that could be worth $1 billion.
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January 6, 2023
San Francisco Business Times – Tapping the power of the CRISPR genome-editing technology, Alameda-based Scribe Therapeutics recently signed a deal with drug maker Sanofi to enable genetic modification of novel “natural killer” cell therapies for cancer.
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November 3, 2022
BioPharma Dive – Read three takeaways from a panel hosted by BioPharma Dive featuring Scribe Therapeutics CEO Benjamin Oakes.
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October 18, 2022
In Vivo – In September, Sanofi received non-exclusive rights to use Scribe Therapeutics, Inc.’s proprietary CRISPR genome editing technologies and platform of wholly owned enzymes to create ex vivo natural killer cell therapies for cancer.
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September 28, 2022
Bio-IT World – The agreement grants Sanofi non-exclusive rights to Scribe’s proprietary CRISPR platform of wholly owned enzymes to create ex vivo NK cell therapies.
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September 28, 2022
Pharmaceutical Technology – Scribe’s CasX-Editors (XE), a suite of custom engineering genome editing and delivery tools based on new foundations such as the CasX enzyme, will back Sanofi’s developing NK cell therapies pipeline for cancer.
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September 27, 2022
Scrip – Sanofi is turning to gene-editing pioneer Jennifer Doudna and her CRISPR-CasX-based Scribe Therapeutics, Inc. to help it take its next steps in developing potential off-the-shelf cancer therapeutics derived from engineered natural killer (NK) cells.
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September 27, 2022
BioWorld – Venture-backed startup Scribe Therapeutics Inc. landed a $25 million up-front payment and a chance at more than $1 billion in milestones by granting Sanofi SA license to genome-editing technology for multiple oncology targets.
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September 27, 2022
BioCentury – Scribe Therapeutics Inc. said Tuesday it will grant Sanofi non-exclusive rights to its CasX-Editor technology for multiple undisclosed oncology targets in engineered NK cell therapies.
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September 27, 2022
The Pharma Letter – Californian genetic medicine company Scribe Therapeutics has scored a major strategic collaboration with French giant Sanofi.
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September 27, 2022
Genetic Engineering and Biotechnology News – Sanofi and Scribe Therapeutics will partner to develop CRISPR-based cell therapies to fight cancer, the companies said today, through a collaboration that could generate more than $1 billion for the CRISPR drug developer whose co-founders include Nobel laureate Jennifer Doudna, PhD, of UC Berkeley.
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September 27, 2022
BioPharma Dive – Sanofi will partner with the Californian biotechnology company Scribe Therapeutics in a deal that extends its exploration of new ways to build cancer cell therapies.
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September 27, 2022
MedCity News – Sanofi is collaborating with Scribe Therapeutics to use the startup’s CRISPR technology to create cell therapies based on natural killers, a type of immune cell that has cancer-killing capabilities.
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September 27, 2022
FirstWord Pharma – Sanofi entered into an agreement to use Scribe Therapeutics’ CRISPR genome editing technologies to enable genetic modification of novel natural killer (NK) cell therapies for cancer.
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September 27, 2022
BioSpace – Under the terms of the deal, Sanofi picks up non-exclusive rights to Scribe’s CRISPR platform of wholly owned enzymes.
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September 27, 2022
Fierce Biotech – Sanofi has teamed up with Scribe Therapeutics to write the next chapter in its natural killer (NK) cell therapy story, paying $25 million upfront and committing to $1 billion in biobucks for access to a CRISPR platform.
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September 27, 2022
Endpoints News – The Paris-based giant’s head of oncology research and its chief of genomic medicine have settled on Scribe Therapeutics’ CasX editing tech for their work on NK cells.
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August 12, 2022
Endpoints News – “CRISPR-by-design” is the idea behind Scribe Therapeutics, a company spun out from Jennifer Doudna’s Nobel-winning lab that’s competing in a closely-tracked field of genome editor companies just starting to make their way to the clinic.
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July 29, 2022
The Real Deal – Scribe Therapeutics, a molecular engineering company, is the latest notable lessee after securing a building at the Research Park at Marina Village in Alameda.
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July 1, 2022
TIME – [Ben Oakes’] team has pioneered a CRISPR system relying on a different enzyme, or DNA-cutting molecule, than the original CRISPR platform, and in animal models of ALS, the system seems to edit the targeted mutations more efficiently and contribute to a longer lifespan for the animals than the original CRISPR platform.
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June 29, 2022
MIT Technology Review – As CEO of Scribe Therapeutics, Benjamin Oakes, 33, is working to optimize novel CRISPR enzymes and ways to package the gene-editing systems to solve those problems.
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May 12, 2022
Genetic Engineering and Biotechnology News – CEO Benjamin Oakes recently discussed the Biogen collaboration, and his company’s progress in developing its genome editing technology, in an exclusive interview with GEN Edge.
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May 4, 2022
Inside Precision Medicine – Biogen has exercised an option for an additional disease target in gene therapy with Scribe Therapeutics. This is part of the companies’ ongoing research collaboration to develop and commercialize CRISPR-based therapeutics.
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May 3, 2022
Pharma Manufacturing – Scribe, headquartered outside of San Francisco, focuses on creating gene therapies using CRISPR technology and custom engineered enzymes. The company’s custom platforms help it to overcome the technological hurdles that other companies in the field face, said Oakes.
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May 2, 2022
Fierce Biotech – Biogen is double-dipping into a 2020 collaboration with Scribe Therapeutics, exercising its option for an additional neurological disease target in gene therapy using the biotech’s CRISPR technology.
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May 2, 2022
Seeking Alpha – Biogen (NASDAQ:BIIB) has exercised an option to develop another gene therapy disease target as part of a collaboration with Scribe Therapeutics.
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April 22, 2022
San Francisco Business Times – Scribe Therapeutics CEO Benjamin Oakes is honored in the San Francisco Business Times’ 40 Under 40 Class of 2022.
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April 11, 2022
BIOS Podcast – An interview with Scribe co-founders Ben Oakes and Dave Savage on the future of genetic medicine.
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April 4, 2022
Science in Society Podcast – A chat with Dr. Benjamin L. Oakes on what CRISPR is, how it revolutionized biological research, and how Scribe Therapeutics will take it to its next generation.
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March 25, 2022
CFO – Biotech firm Scribe Therapeutics appointed David Parrot as chief financial officer. Parrot joins the company from Barclays, where he was a managing director responsible for building its West coast life sciences and biotechnology investment banking business.
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March 21, 2022
CFO Dive – Former Barclays executive David Parrot is bringing a number of lessons learned from his more than two-decade career in life sciences investment banking to his new role as CFO of biotech firm Scribe Therapeutics.
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March 11, 2022
Fierce Biotech – David Parrot is the new CFO of Scribe Therapeutics, a molecular engineering company focused on CRISPR-based meds, after serving as a managing director at investment bank Barclays.
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March 11, 2022
Endpoints News – One of Jennifer Doudna’s CRISPR startups, Alameda, CA-based Scribe Therapeutics, has corralled David Parrot as CFO and George Manning as controller.
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March 11, 2022
BioSpace – Life sciences companies continue to bolster their leadership teams as they prepare for the next phase of growth.
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March 10, 2022
The Wall Street Journal – Scribe Therapeutics Inc., an Alameda, Calif.-based biotech startup also co-founded by Dr. Doudna, is developing custom-engineered enzymes for Crispr-based treatments for neurodegenerative and other diseases. Scribe’s technologies are distinct from earlier approaches, co-founder and CEO Benjamin Oakes said.
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March 10, 2022
BioCentury – Scribe Therapeutics Inc. hired David Parrot as CFO. Parrot was managing director, head of west coast life science investment banking at Barclays Investment Bank. Scribe is developing custom enzymes and delivery modalities for CRISPR and was co-founded by Jennifer Doudna.
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March 10, 2022
BioWorld – Scribe Therapeutics Inc., of Alameda, Calif., appointed David Parrot chief financial officer and George Manning controller.
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January 31, 2022
Business Insider – With a busy 2022 ahead for the gene-editing industry, Insider identified the top 18 companies to know that are leading the space.
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January 5, 2022
Genetic Engineering and Biotechnology News – Scribe scientists hone CasX enzymes so that they acquire characteristics such as enhanced specificity. Oakes describes this as an “engineering first” philosophy, where the desired properties of the system are chosen in advance and intentionally designed, rather than being left to chance or nature.
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December 28, 2021
Business Insider – Scribe’s main enzyme, CasX, is also smaller and more efficient at making edits, Oakes said. This group of companies often searches nature for new enzymes and then tinkers with them in a lab, aiming to make a better editing tool at the end.
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November 4, 2021
California Life Sciences – Scribe Therapeutics named Rising Star in the 2021 Pantheon Awards recognizing companies and individuals making significant scientific, business, and community contributions across California.
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October 26, 2021
Biocom California – Scribe Therapeutics CEO Benjamin Oakes selected as a winner of the 6th annual Catalyst Awards.
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August 16, 2021
Business Insider – Scribe CEO Benjamin Oakes is carving out a space in the gene-editing field by developing what he calls a “genetic scalpel.”
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July 28, 2021
Business Insider – Cofounded by CRISPR discoverer Jennifer Doudna and two former researchers in her University of California lab, Scribe is pursuing its own twist on CRISPR. While the standard gene-editing approach uses an enzyme called Cas9, Scribe is developing a smaller version called CasX, which could allow for more applications of CRISPR.
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May 6, 2021
MedTech Breakthrough Awards – Scribe Therapeutics wins Best New Technology Solution – Drug Development.
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May 5, 2021
Fast Company – Medical innovations that save lives, extend longevity, or increase access to care.
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April 29, 2021
Bio-IT World – $100M: Series B for Custom Gene Editing. The capital will be used to further develop Scribe’s suite of custom gene editing and delivery technologies, as well as to advance a pipeline of therapeutics for neurodegeneration and additional diseases with high unmet need.
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April 12, 2021
Nanalyze – The company has raised a whopping $120 million from the likes of Andreessen Horowitz to build out a suite of CRISPR technologies designed to treat genetic diseases.
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April 8, 2021
a16z Bio Clubhouse – a16z general partners Vineeta Agarwala and Vijay Pande talk to guest Ben Oakes, cofounder, President and CEO of Scribe Therapeutics in a conversation on the power of engineering gene editors, the transition from academia to a startup, and how to select the first indication to target with a novel bio platform.
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April 6, 2021
Endpoints News – The annual 20 Under 40 list features CEO Benjamin Oakes and how his dive inside the human mind colors his leadership role at gene editing startup Scribe Therapeutics.
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April 1, 2021
PMLiVE – Scribe’s technology platform can create custom CRISPR molecules that are specifically designed for therapeutic use within the body, overcoming the limitation of using existing enzymes that may lead to ‘poor editing outcomes’.
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March 31, 2021
Endpoints News – The California-based biotech will use that cash to continue developing their engineering platform, while bringing forward a pipeline that includes a Biogen-partnered ALS treatment.
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March 31, 2021
Chemical & Engineering News – The start-up is applying protein engineering to create new CasX enzymes for neurodegenerative diseases and more.
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March 31, 2021
FierceBiotech – Rather than “shoehorning” enzymes that evolved to work well in bacteria—but not in humans—into treatments for human disease, Scribe is engineering CRISPR molecules from scratch.
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March 31, 2021
Forbes – Instead of relying on wild-type or naturally occurring Crispr molecules such as Cas9, Scribe Therapeutics have built their own, highly-specialized varieties.
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March 31, 2021
Crunchbase News – Molecular engineering company Scribe Therapeutics has completed an oversubscribed $100 million round of Series B financing to further develop its “CRISPR by design” platform, as well as advance its pipeline of genetic treatments.
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March 31, 2021
Genetic Engineering & Biotechnology News – Scribe—one of a new wave of gene editing biotech companies—focuses on developing CRISPR-based treatments through its genetic modification platform, designed to build and apply its suite of CRISPR technologies designed for therapeutic use.
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March 31, 2021
BioWorld – Scribe Therapeutics Inc. raised $100 million in a series B round to continue its engineering-intensive approach to developing CRISPR-based therapies that employ custom-designed CasX enzymes.
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March 31, 2021
Technology Networks – Scribe Therapeutics co-founder and CEO Benjamin Oakes sat down for an interview on the company’s next steps in “fulfilling the promise of CRISPR” and how it will navigate some of the challenges associated with developing CRISPR-based therapeutics, including efficacy, scale-up and high costs.
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March 31, 2021
San Francisco Business Times – The Alameda-based biotech startup will use the fresh capital to expand its team and advance the company’s specialized approach to gene editing in the hopes of creating new treatments for a host of unmet diseases.
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January 14, 2021
Barron’s – Gene editing is advancing so quickly that next-generation technologies are already on the heels of Crispr-Cas9.
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January 6, 2021
BioSpace – The NextGen Bio Class of 2021 is a stellar group of companies that are already making an enormous impact on the industry now and will continue into the future.
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December 14, 2020
Medium – Future Human – Scribe Therapeutics of Alameda, California, is using yet another form of CRISPR dubbed X-editing. Co-founded by CRISPR pioneer and Nobel winner Jennifer Doudna, PhD, the company will use the new gene-editing tool to develop treatments for neurological diseases.
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November 18, 2020
The Scientistt Podcast – Benjamin L. Oakes is the Founder and CEO of Scribe Therapeutics, a company rewriting the story of disease and engineering the future of genetic medicine.
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November 3, 2020
Nature Biotechnology – Startup Scribe Therapeutics, spun out of Jennifer Doudna’s lab, emerged from stealth on 6 October with a next-generation CRISPR technology, armed with a $20-million series A round and a collaboration with Biogen.
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October 20, 2020
Biocom – Another of Doudna’s spin-outs, Scribe Therapeutics, just recently announced their plans to build a platform for CRISPR-based genetic medicine to create therapies for diseases like genetically driven ALS. The company’s tools and mission have the potential to dramatically accelerate CRISPR’s applications into the clinical setting.
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October 19, 2020
CRISPR Medicine News – California-based gene-editing company Scribe Therapeutics recently unveiled its plans to develop the most advanced platform for breakthrough CRISPR-based genetic medicines.
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October 8, 2020
Genetic Engineering & Biotechnology News – Best known for her pioneering work in the discovery of CRISPR, Jennifer Doudna, PhD, professor at the University of California, Berkeley, doesn’t stop or, it seems, even slow down. As of yesterday morning, Doudna can add “accept Nobel Prize” to her to-do list as she, along with Emmanuelle Charpentier, PhD, was awarded the 2020 Nobel Prize in Chemistry.
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October 8, 2020
ALS News Today – Founded by the scientists who originally invented CRISPR, Scribe has developed novel, custom-CRISPR tools, using a technology called X-Editing. This advanced gene-editing platform has greater editing activity and higher specificity, meaning that it can edit the target gene with greater precision than other CRISPR tools currently available.
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October 8, 2020
pharmaphorum – Scribe Therapeutics, a start-up focusing on gene-editing using CRISPR/Cas9, has burst onto the biotech scene with a $415 million deal with Biogen.
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October 8, 2020
Clinical OMICs – This week, another Doudna lab spin out, Scribe Therapeutics, came out of stealth mode to announce their plans to build a platform for CRISPR-based genetic medicine with news of a new Biogen collaboration to create therapeutics for genetically-driven ALS.
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October 7, 2020
Pharmaceutical Business Review – Molecular engineering company Scribe Therapeutics has entered into a research collaboration with Biogen for the development of CRISPR-based genetic medicines for neurological diseases.
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October 7, 2020
FierceBiotech – CRISPR evolved in bacteria as a form of “genetic vandalism,” as George Church, Ph.D., puts it, to fend off pathogens. That means it works very well in bacteria but runs into various obstacles when researchers try to put it to work in humans. Jennifer Doudna’s latest CRISPR company plans to surmount those hurdles with an entirely new CRISPR platform that does not rely on molecules found in nature.
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October 6, 2020
BioWorld – Scribe Therapeutics Inc., another CRISPR-based genome editing firm out of the Jennifer Doudna stable, launched with $20 million in series A funding and a deal with Biogen Inc. in amyotrophic lateral sclerosis (ALS), which brings in another $15 million up front and up to $400 million in development and commercial milestones.
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October 6, 2020
BioCentury – Scribe is carving out a new space in the gene editing landscape with a next-generation version of the technology from Jennifer Doudna’s lab that substitutes engineered CRISPR enzymes for their natural counterparts.
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October 6, 2020
San Francisco Business Times – Hoping to take the CRISPR genome-editing tool to the next level of drug development, startup Scribe Therapeutics Inc. said Tuesday that it landed a potential $400 million neurodegenerative disease deal with Biogen Inc.
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October 6, 2020
Xconomy – The first generation of CRISPR-based therapies showed how the technology can edit DNA, making genetic fixes to unwanted mutations. But those treatments use the CRISPR system as scientists found it in nature, which means it still has limitations when applied to humans, says Benjamin Oakes, CEO of Scribe Therapeutics.
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October 6, 2020
Chemical & Engineering News – Scribe Therapeutics, a biotech firm focused on developing next-generation gene-editing technology, has raised $20 million in its first major round of financing, backed by Andreessen Horowitz. The firm separately unveiled a deal with Biogen to develop CRISPR-based treatments for amyotrophic lateral sclerosis (ALS).
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October 6, 2020
Endpoints News – Three years ago, Jennifer Doudna gathered with two postdocs and a fellow biochemist around a circular table on the second floor of UC Berkeley’s energy biosciences building, where they tried to answer a question: What, precisely, would the best gene editor look like?
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October 6, 2020
San Francisco Business Times – Jennifer Doudna’s string of companies, including an Alameda startup, have covered everything from agriculture to a Covid diagnostic to potential drugs.
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October 6, 2020
Reuters – U.S. drugmaker Biogen Inc and gene-editing startup Scribe Therapeutics Inc will jointly develop therapies for treating underlying genetic causes of amyotrophic lateral sclerosis (ALS), a fatal neurological disorder better known as Lou Gehrig’s disease.
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October 6, 2020
TechCrunch – A new company called Scribe Therapeutics founded by two former members of CRISPR pioneer Jennifer Doudna’s UC Berkely genetics lab (alongside Doudna herself) launched on Tuesday, debuting a platform designed specifically to help develop and engineer new therapeutics based on CRISPR for addressing specific diseases, with permanent treatments in patients.
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October 6, 2020
Forbes – What if you had a tool to change the genetic instructions that cause disease? That’s what San Francisco-based Scribe Therapeutics hopes to do with its next-generation platform for gene editing.
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December 2, 2019
Chemical & Engineering News – Jennifer Doudna’s lab at the University of California, Berkeley, published a detailed study on a genetically and structurally distinct CRISPR enzyme called CasX, which makes staggered breaks during its cutting of the DNA double helix.
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February 10, 2019
Chemical & Engineering News – CasX, first described in 2016, is smaller than its more famous cousins, Cas9 and Cas12a. This makes it a potentially better candidate for medicinal use as the field turns to viruses to try to get CRISPR systems into the human body.
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February 6, 2019
Drug Discovery & Development – While CRISPR Cas9 remains a mainstay in the genomics world, researchers have now found a much smaller protein called CasX that could be used for gene editing.
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February 6, 2019
New Atlas – In new tests, the researchers have found that it is effective at editing the human genome, as well as that of E. coli.
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February 6, 2019
Interesting Engineering – New research is now revealing CasX is a viable alternative to Cas9. The gene editor was sourced from a microbe database found in groundwater and sediment, and it works in both bacteria and human cells.
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February 5, 2019
Silicon Republic – CRISPR-Cas9 has revolutionised gene editing, but a new variant of the technology may be far superior.
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February 5, 2019
Futurism – Researchers from UC Berkeley have discovered that CasX is capable of editing human cells, and it doesn’t carry with it some of the issues involved in Cas9 editing — potentially putting us one step closer to safely gene-editing humans.
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