Solving the Upstream Bottleneck in Cell Collection to Enable Scalable Advanced Therapy Delivery
Advanced cell and gene therapies (CGTs) are transforming medicine, offering new hope for patients with cancers, genetic disorders and autoimmune diseases once considered untreatable. Yet despite their promise, these therapies face major challenges in scaling and gaining broader market access. Fragmented infrastructure, limited provider capacity, outdated clinical guidelines and complex logistics all stand in the way of equitable patient access.
A critical and often overlooked pressure point in this system is upstream cell collection. Apheresis, specifically leukapheresis, is the foundation for most CGTs, whether autologous or allogeneic. However, access remains tightly bound to centralized academic centers, which restricts scalability and limits patient reach.
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