Technologies
Accelerating the Development and Commercialization of Revolutionary Therapeutics.
Pluristyx Technologies
Pluristyx has curated a portfolio of innovative technologies aimed at enhancing and enabling allogenic cell therapies. Our proprietary techniques have been designed by an executive team with over 50 years of expertise and industry experience aiming to reduce issues commonly faced by the cell therapy field.
The Pluripotent Stem Cell (iPSC) Solution has a lot of promising qualities and potential for treating currently incurable diseases. Pluristyx is ready to enable, Tomorrow’s Cell Therapies Today®.
Patent protected technologies
With our enlarged portfolio of unique non-modified and genetically engineered iPSC-based technologies, we can assist you at any stage in establishing proof of concept through to commercialization.
One Cell For All
Offering an array of gene editing technologies resulting in unparalleled functional control of commercial products.
Click on our technologies to learn more
FailSafe®
Cellular Reprogramming
iACT Stealth Cells™
Cryopreservation
REA Process & Licensing
Simplifying Stem Cell Production
Pluristyx's portfolio of technologies makes the complicated induced pluripotent stem cell (iPSC) manufacturing simple by shortening the development lifecycle and removing the common barriers that block the translation of tomorrow’s cell therapies to the clinic. With full control of the upstream workflow, Pluristyx can help you select, license, genetically edit, and manufacture stem cells all under one roof.
Our Products
Our Cellular Reprogramming technology provides clients access to high quality induced Pluripotent Stem cells (iPSC) that can be gene edited to incorporate our proprietary platform gene edits FailSafe® and iACT Stealth Cells™.
These technologies combat the two of the major challenges identified in cell therapy: the risk of immune rejection when using cells from universal donors and concerns regarding the safety of gene-engineering. Our stem cells can be accessed for a low upfront cost to help select an appropriate line that will generate your downstream cellular product.
iPSC
Human pluripotent stem cells (iPSC) for use in R&D activities. Inquire for GMP grade cells suitable as a starting material in clinical applications.
Custom iPSC
Pluristyx can employ our mRNA reprogramming technology to generate custom hiPSC lines based on your specific requirements. Custom hiPSCs can be further modified to include our proprietary FailSafe® or iACT Stealth Cells™ technologies, as well as your custom genetic edits to generate the ideal starting material for your downstream product development and clinical manufacturing.
Differentiated Cells
iPSC
Human pluripotent stem cells (iPSC) for use in R&D activities. Inquire for GMP grade cells suitable as a starting material in clinical applications.
Custom iPSC
Pluristyx can employ our mRNA reprogramming technology to generate custom hiPSC lines based on your specific requirements. Custom hiPSCs can be further modified to include our proprietary FailSafe® or iACT Stealth Cells™ technologies, as well as your custom genetic edits to generate the ideal starting material for your downstream product development and clinical manufacturing.
Differentiated Cells
The panCELLa Platform:
The Solution
Developing the next generation of stem cell therapies is slow, hard, and expensive. Pluristyx offers a solution: the panCELLa platform. Through our platform, we take on the most difficult parts of your stem cell process, including CMC support, process and analytical development services, gene editing, and cell line development, to help you convert your concept into a clinical reality.
70% reduction in development time
Proprietary technology with clear freedom to operate
Fastest path to clinic
Solutions
Developing the next generation of stem cell therapies is slow, hard, and expensive. Pluristyx has the expertise needed to take on the most difficult parts of your stem cell process, including CMC support, process and analytical development services, gene editing, and cell line development, to help you convert your concept into a clinical reality.