Cell and gene therapy company NewBiologix exits stealth with $50M

cell therapy

NewBiologix SA has emerged from stealth as a technology innovation company developing a proprietary and breakthrough platform for the advanced engineering of cell lines used to manufacture gene and cell therapies. 

The company’s DNA-based platform is being developed to address key manufacturing challenges associated with the production of recombinant adeno-associated virus (rAAV) vectors used to produce advanced therapy medicinal products (ATMPs). NewBiologix’s $50 million series A was led by Recipharm A/S with additional funding from the company’s co-founders, Igor Fisch and Nicolas Mermod.

“As the number of gene and cell therapies in the clinic and market continues to grow, improved manufacturing solutions for viral vectors are needed,” said NewBiologix co-founder and CEO, Igor Fisch, who brings more than 20 years’ experience in biotech and cell line development to the new entity. 

“Our mission is to help biopharmaceutical companies treat some of the most devastating diseases by providing them with innovative technologies and solutions to boost the production and efficacy of viral vectors, rapidly and more cost effectively.”

NewBiologix focuses on adeno-associated virus vectors

NewBiologix is currently focused on recombinant adeno-associated virus (rAAV) vectors, the preferred delivery vehicle for gene therapies. The company’s technologies will be applied to human (HEK-293) and mammalian (CHO) cell lines. These cell lines will be engineered to be readily adaptable to meet the viral vector demands and requirements over a full range of therapeutic indications to help partners address rare, chronic, and currently incurable diseases. Cell lines engineered with NewBiologix’s innovative platform will allow for more stable rAAV production, higher quality and predictable expression levels, less empty capsids, and better batch-to-batch reproducibility of production.

“Current gene and cell therapies primarily focus on rare diseases. We believe our approach to generating rAAV vectors should help biopharmaceutical companies advance into emerging therapies that target larger patient populations with chronic conditions,” said NewBiologix co-founder and senior vice president of research and development, Nicolas Mermod, also a 20-year biotech veteran with expertise in molecular biotechnology. 

“NewBiologix’s platform is a quantum leap forward. Our approach will significantly impact the cost of goods sold (COGs), making gene therapy more viable for rare diseases.”

NewBiologix is leveraging next-generation sequencing (NGS)-based genome characterization to develop a proprietary bioinformatics platform designed to improve cell line capabilities for the expression and production of ATMPs. By including NGS-based technologies during the cell line development process, NewBiologix said it can make data-driven decisions about the cell banks’ stability, integrity, and biosafety while providing robust supportive data for regulatory submissions.

The Swiss Health Valley based company will begin beta testing the cell line prototypes with key collaborators by 2024 and anticipates making viral production cell lines commercially available by 2026.

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