Jake Krembil, COO of panCELLa and Brian Hawkins, CTO of Pluristyx-
“Pluripotent Stem Cells have the potential to generate any tissue in the body, and are the next wave of advanced cell therapies. We are excited to introduce our merged company as a leading provider of these genetically modified stem cells for both research and clinical use,” states Brian Hawkins, CTO of Pluristyx.
The two companies recognized the potential for synergies resulting from their complementary competencies, leading to a merger agreement and the establishment of a unified organization. The newly formed company is equipped to provide clients with high-quality iPSC lines that allow allogeneic cell therapy from research to clinical and commercial scale. The merger’s primary goal is to offer capabilities and enable clients an accelerated path into the market.
The merger will amalgamate Pluristyx’s proficiency in cell therapy development with panCELLa’s avant-garde technology for generating high-quality, scalable, and consistent pluripotent stem cells. The combined enterprise will deliver comprehensive, state-of-the-art solutions to its clientele by fusing panCELLa’s remarkable genetic editing technologies and patents with Pluristyx’s capacity to produce induced pluripotent stem cell (iPSC) lines at a commercial scale. This integration of technology and service offerings will expedite the delivery of groundbreaking cell therapies to patients as they are needed.
“The new entity offers end-to-end stem cell services to clients, from cell sourcing and manufacturing to clinical development and commercialization,” says Brian Hawkins, CTO of Pluristyx.
“The merger of Pluristyx and panCELLa will create a single entity that will be well-positioned to become a leader in the development and commercialization of advanced cell therapies,” adds Jake Krembil,COO of panCELLa
Remarkably, the superior quality iPSCs generated by the merged organization through an exclusive mRNA-based technology can be procured under a ‘try-before-you-buy’ research evaluation model. This research evaluation model allows groups to evaluate both the underlying iPSC line and genetically edited variants for a low upfront fee prior to making a licensing decision. Common genetic edits available under our research evaluation model include our proprietary iACT® and FailSafe® technologies, which respectively allow cells to avoid rejection by the patient’s immune system and provide a means to eliminate cells from patients when they are no longer needed.
By providing end-to-end services to clients throughout their product development journey, the new entity will be well-equipped to accelerate the delivery of revolutionary treatments to patients and provide the fastest path to gene-edited iPSC-based therapies. The collaboration is poised to revolutionize the production and delivery of cell therapies, offering a promising outlook for addressing previously untreatable diseases.


