Merck has announced a strategic alliance in the CRISPR/Cas9 rodent model market with France-based biotechnology company genOway.
“We are committed to making our patented CRISPR technology broadly available to the global research and discovery community,” said Udit Batra, member of the Merck Executive Board and CEO, Life Science. “Together with genOway, we will get the best research models out to the pharmaceutical and biotech industries as well as academic laboratories quickly, so we can help accelerate their research, shorten drug development timelines and treat previously untreatable diseases in faster and more targeted ways. We will continue to play an active role, responsibly and ethically, in ensuring that scientists have access to the latest CRISPR technologies.”
Through an exclusive worldwide license of Merck’s foundational CRISPR integration patents, genOway will develop new models and solutions allowing non-profit and for-profit scientists to use CRISPR/Cas9 technology. Under the agreement, genOway will also develop a network of sublicensees in both the model creation and distribution businesses and preclinical services for all potential applications worldwide, with a strong focus in the United States, Asia and Europe. Financial details were not disclosed.
Both Merck and genOway have identified research fields where they can combine their respective technologies and expertise to develop and validate new CRISPR/Cas9-related products and solutions. Merck’s patented CRISPR integration technology is a strong entry point through which innovation can be developed and launched.
“The CRISPR/Cas9 IP landscape has been complex and uncertain over the last years,” said Alexandre Fraichard, CEO of genOway. “The situation has changed and the Merck IP portfolio is clearly central to CRISPR/Cas9-based eukaryotic genome-editing applications. This alliance, combining research and business, will enable us to provide the scientific community with more physiologically relevant models and the necessary intellectual property rights which will ultimately speed delivering better drugs to patients.”
CRISPR technology is a core competency for Merck, which has 14 years’ experience with genome editing, spanning from discovery to manufacturing. Merck recognizes that genome editing has resulted in major advancements in biological research and medicine. At the same time, the growing potential of genome-editing technologies has opened scientific, legal and societal concerns. As both a user and supplier of genome-editing technology, Merck supports research with genome editing under careful consideration of ethical and legal standards. Merck has established an independent, external Bioethics Advisory Panel to provide guidance for research in which its businesses are involved, including research on or using genome editing, and has developed, defined and transparently published a clear operational position taking into account scientific and societal issues to inform promising therapeutic approaches for use in research and applications.