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Page Background

Bespoke individualised therapies – complex logistics

Automated manufacture

Expensive

Allogeneic CAR-T

Antigen escape relapses

Targeting multiple antigens – single CAR construct, multiple CAR constructs, multiple cellular products

Clinical challenges

Durability of responses?

Defining cell dose, optimal lymphodepletion

Positioning in overall treatment pathway

Optimal approach to limit or manage toxicities

CAR19: challenges