Tuesday, January 27, 2026
There is significant opportunity to expand the applications of cell therapy further into rare diseases as well as to tackle widespread conditions.
As cell and gene therapy shifts toward in vivo approaches and regenerative modalities — iPSCs, MSCs, HSCs, and beyond — sponsors face new challenges beyond traditional CAR-T manufacturing: bioreactor and culture system selection, analytical strategy, and potency assay development for cell types with far less manufacturing precedent.