AI Article Synopsis

  • * The white paper from JSRM and ISCT discusses obstacles related to regulatory differences, safety testing, and manufacturing costs in developing iPSC therapies.
  • * It emphasizes the need for consistent global guidelines and advanced manufacturing processes to ensure the safety and affordability of iPSC-based treatments for broader adoption.

Article Abstract

Since their first production in 2007, human induced pluripotent stem cells (iPSCs) have provided a novel platform for the development of various cell therapies targeting a spectrum of diseases, ranging from rare genetic eye disorders to cancer treatment. However, several challenges must be tackled for iPSC-based cell therapy to enter the market and achieve broader global adoption. This white paper, authored by the Japanese Society for Regenerative Medicine (JSRM) - International Society for Cell Therapy (ISCT) iPSC Committee delves into the hurdles encountered in the pursuit of safe and economically viable iPSC-based therapies, particularly from the standpoint of the cell therapy industry. It discusses differences in global guidelines and regulatory frameworks, outlines a series of quality control tests required to ensure the safety of the cell therapy, and provides details and important considerations around cost of goods (COGs), including the impact of automated advanced manufacturing.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11471376PMC
http://dx.doi.org/10.1016/j.jcyt.2024.05.022DOI Listing

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