BioPharma, Artificial Intelligence

CRISPR-editing biotech Arbor Bio adds $215M for liver, CNS disease therapies

Arbor Biotechnologies raised new cash to keep up the pace in the chase for new genetic medicines. The MIT spinout applies artificial intelligence and machine learning to discover CRISPR enzymes applicable for gene-editing therapies; the Series B financing comes as programs in liver and central nervous system disorders move closer to human testing.


Arbor Biotechnologies, a genetic medicines company that claims to have the most extensive gene-editing toolbox in the industry, is also building a substantial war chest. The company has raised $215 million in financing as it works to advance its lead programs toward clinical testing.

The Series B financing announced Tuesday was led by Temasek, Ally Bridge Group, and TCG Crossover.

Cambridge, Massachusetts-based Arbor, uses machine-learning techniques and artificial intelligence to mine its database of billions of proteins. Doing so enables the company to discover the enzymes that have potential use in CRISPR gene editing. Cas9, a type of enzyme called a nuclease, might be the best known of the cutting enzymes used in CRISPR editing. Arbor claims that it has discovered more than 60 nuclease families as well as more than 70 CRISPR transposases, another type of enzyme. Arbor’s CRISPR toolbox encompasses DNA nucleases, RNA nucleases, and transposases. The company uses those enzymes in its genetic medicines, which are designed to edit the genetic errors that cause disease.

So far, Arbor is preclinical. The company’s lead programs are for liver and central nervous system diseases. In a prepared statement, Arbor CEO Devyn Smith said Arbor plans to use the new capital to advance those programs toward clinical testing. The cash will also be used to advance pipeline programs and to support further investment in its discovery technology.

“While our primary focus has been on developing our bespoke CRISPR nucleases, we are also looking to progress our other precision editing innovations, such as CRISPR transposases,” Smith said.

Sponsored Post

Physician Targeting Using Real-time Data: How PurpleLab’s Alerts Can Help

By leveraging real-time data that offers unprecedented insights into physician behavior and patient outcomes, companies can gain a competitive advantage with prescribers. PurpleLab®, a healthcare analytics platform with one of the largest medical and pharmaceutical claims databases in the United States, recently announced the launch of Alerts which translates complex information into actionable insights, empowering companies to identify the right physicians to target, determine the most effective marketing strategies and ultimately improve patient care.

The financing is the latest development in what has been a busy year for Arbor. The company has brought on a flurry of new hires, including Smith, who joined in April. The company has also been making business development progress. In August, Vertex Pharmaceuticals inked a new partnership with Arbor, expanding on an alliance initially begun in 2018.

Under the new pact, Boston-based Vertex will use Arbor’s CRISPR gene-editing technology for the research and development of new ex-vivo cell therapies. At the top of Vertex’s wish list is engineering islet cells, a type of cell in the pancreas that produces insulin, as a potential new therapy for type 1 diabetes. Vertex is also interested in developing therapies for blood disorders sickle cell anemia and beta thalassemia. The upfront payment to Arbor was not disclosed but the companies said that potential milestone payments could reach up to $1.2 billion.

Applications of CRISPR in therapeutic applications has moved toward smaller cutting enzymes that leave more room for additional cargo Arbor has published research about Cas13d, stemming from the company’s technology platform. The enzyme is part of the Cas13 family. Its smaller size makes it applicable for RNA manipulation and detection.

However, Arbor faces competition in the race to go smaller, particularly as biotechs pursue gene-editing therapies that do their work in vivo—inside the patient. Mammoth Biosciences touts a toolbox that includes Cas14 and CasPhi enzymes, which are both smaller than Cas9. South San Francisco-based Mammoth announced a $150 million Series D round of funding in September. Late last month, Mammoth and Vertex announced an alliance focused on developing in vivo gene-editing therapies for two undisclosed genetic diseases. The deal pays Mammoth $41 million up front, with $650 million more tied to milestones.

Arbor was founded in 2016, based on research from MIT. The biotech raised a $15.6 million Series A round of funding in 2017. The latest financing added new investors Arrowmark Partners, Deep Track Capital, Great Point Ventures, Illumina Ventures, Janus Henderson Investors, Logos Capital, Ono Venture Investment, Piper Heartland Healthcare Capital, Ridgeback Capital Investments, Section 32, Surveyor Capital, T. Rowe Price Associates, Tao Capital Partners, funds managed by Tekla Capital Management, Woodline Partners, and a global investment fund that was undisclosed. Additionally, Vertex also invested, as well as earlier investor ARCH Venture Partners.

Photo by Flickr user Jason Baker via a Creative Commons license