Cat Lutz named Vice President of Rare Disease Translational Center at The Jackson Laboratory

Cat Lutz , Ph.D., M.B.A. was recently named vice president of the Rare Disease Translational Center at The Jackson Laboratory, a nonprofit biomedical research institution headquartered in Bar Harbor, Maine. With this appointment, JAX marks an important step in the expansion of its commitment to rare disease research.

For the past six years, The JAX Rare Disease Translational Center has worked with dozens of rare disease foundations and their associated research teams to generate custom mouse models that represent rare conditions in order to pursue new therapeutic interventions. Using CRISPR/Cas9 precision genome engineering, the Center’s expertise has been in assessing the mouse models currently available for rare disorders, determining if new resources are needed and studying rare diseases through these models.

With this expansion, the Center will enlarge its focus to play an integral role throughout theentire rare disease odyssey – from diagnosis to research to drug development. Utilizing the resources of The Jackson Laboratory for Genomic Medicine based in Farmington, Conn., the Rare Disease Translational Center will partner with hospitals and medical institutions as they diagnose rare diseases. In addition, the Center will collaborate more closely with biotech and pharmaceutical companies to strategize and tailor therapeutics with the aim of accelerating the path to drug discovery for these debilitating conditions. By taking a more holistic approach, the Center will be better positioned to make a significant impact in the lives of those living with rare diseases.

“JAX is honored to play such a unique role in the fight against rare diseases,” said Lon Cardon, Ph.D., FMedSci., president and CEO of The Jackson Laboratory. “As a nonprofit organization, we focus on enabling and empowering medical progress for rare diseases of all kinds by collaborating with top academic research institutions, foundations ranging from family-run to global in scope, and companies that are using the latest technologies to produce therapeutics for rare disease communities. We are proud that so many organizations work with the JAX Rare Disease Translational Center to accelerate the scientific progress for the rare disease community. This expansion is an important step in our shared quest to improve human health.”

Under Lutz’ leadership, the Center will bring together core capabilities in genetic engineering, phenotyping andin vivo pharmacology to support research and therapeutic advancement for patients and families with rare diseases. The program will expand to further leverage developing technologies in genetic medicine and delivery, using the extensive collection of mouse models that exist in JAX’s repository as well as newly engineered models at JAX.

“I’m extremely honored to be in a position that allows me to focus on the incredible people who make up the rare disease community,” said Cat Lutz, Ph.D., M.B.A. “After over 25 years in this field, and with the growth of the Center, I’m thrilled to continue and expand on the work we have been doing to make strides for this community.”