We are conducting a research collaboration with Oslo University Hospital led by Dr. Karl-Johan Malmberg, a leading expert in NK cell biology and killer cell immunoglobulin-like receptors. Our specific goals of this collaboration are to identify NK cell modifications that promote persistence and enhanced anti-tumor potency, and to create new iPSC-derived NK cell product candidates for development.

We are conducting a research collaboration with the University of Minnesota led by Jeffrey S. Miller, M.D., Deputy Director of the Masonic Cancer Center and the Deputy Director of the Clinical and Translational Science Institute at the University of Minnesota. Under the collaboration, we advanced the first-ever iPSC-derived cell therapy, FT500, and the first-ever engineered iPSC-derived cell therapy, FT516, into clinical development in the United States. We continue to work in collaboration with the University of Minnesota on the research and development of off-the-shelf, iPSC-derived CAR NK cell cancer immunotherapies.

We are collaborating with ONO Pharmaceutical to develop and commercialize off-the-shelf CAR-T cell product candidates for the treatment of solid tumors. The collaboration brings together ONO’s global leadership and proven track record in oncology and our expertise with induced pluripotent stem cells (iPSC) and CAR-T cell therapies. Under the collaboration, using our proprietary iPSC platform, collaboration candidates will be derived from a clonal master iPSC line engineered to completely eliminate endogenous TCR expression, include insertion of a chimeric antigen receptor (CAR) into the TRAC locus and incorporate other anti-tumor functionality.

In June 2022, we expanded our collaboration with Ono to include the research and development of CAR-targeted natural killer (NK) cell candidates derived from engineered master induced pluripotent stem cells for the treatment of solid tumors. We are jointly conducting research and development activities under a joint development plan and are developing product candidates against two solid tumor antigen targets.