Efficient reprogramming of fibroblasts into iPSCs using mRNA technology
Sebastian Diecke, Hannah Johannsen, Parivash Nouri
Cell sorting for enrichment of neuronal subpopulations – new perspectives for clinical research
Thomas Andreska, Elisa Nent, Chengjun Jin
How patient focus drives clinical trial results: the intersection of sponsor, CRO, site, and patient
K Kane, K Nealon, B Bratrude et al
Expand your T cell manufacturing capacities in an automated, closed system to shorten your production time
Sophia Lollies, Ian Johnston
Overcoming challenges in scaled manufacturing of iPSC-derived cells
A Steinbach, D Mann, M Diakatou et al
Optimizing the cell therapy patient journey through integrated CRO/CDMO partnership
Panteli Theocharous, Rupa Pike
Manufacturing and testing a clinical-grade AAV vector: from concept to clinic
Chris Edwards, James Cody
Next-generation CRISPR mRNA-LNPs and scale up manufacturing for CAR T cells
Reka Geczy, Bernice Thommandru
Patient-derived organoids: an emerging platform to de-risk immunotherapy development
Sylvia F Boj, Andrea Bisso
Understanding donor characteristics to improve allogeneic cell therapy outcomes for all
Abeer Madbouly, Martin Maiers, Stephen Sullivan
Navigating scalability and consistency in the allogeneic supply chain
Anne Dircks, Dean Lee MD PhD
Circulating tumor DNA as a predictive biomarker for immunotherapy response: from clinical trials to clinical practice
Michael Krainock, Alan Tan, John Simmons
Accelerating cell therapy discovery & development with non-viral gene engineering
David Hermanson, Xiaobai Patrinostro, Scott Silaika
Discovery to manufacturing: A continuum
Audrey Chang, Tony Hitchcock, Brian Fry