De‑risking AAV scale‑up: process comparability data from a 50 m² fixed‑bed model
Cell & Gene Therapy Insights 2026; 12(6), 679–690
DOI: 10.18609/cgti.2026.081
Published: 2 September
Innovator Insight
Can a 50 m² fixed-bed bioreactor stand in for a 500 m² AAV manufacturing process? Manufacturing science and technology (MS&T) engineers at Novartis Gene Therapies ran five batches on the iCELLis™ platform to find out, comparing process parameters and bulk harvest titers across scales at a fraction of the cost of a manufacturing run. One unplanned transfection deviation was followed by a 48% higher bulk harvest titer.
What you will learn
01
How Novartis Gene Therapies used a Quality by Design framework to decide which process parameters to match, and which to compromise, when scaling down an adherent AAV process
02
Why falling film height, rather than linear speed, became the main lever for dissolved oxygen control at 50 m²
03
How biomass capacitance flagged a seeding deviation early in a run, before it could affect downstream performance
Key interests