The Logistics of Delivering Cell and Gene Therapy Medicines – from Clinical to Commercialization
Alogeneic therapies can be manufactured in large batches, from unrelated donor sources, making the supply chain more predictable. On the other hand, autologous therapies are vein-to-vein with a circular supply chain starting and ending with the patient, adding a layer of complexity to logistics.
Regardless, as with most drugs, the challenge is to move from the clinical stage to commercialization quickly and affordably. No easy task, considering a clinical trial for cell and gene therapies could start with as few as 15 or 30 patients with the goal of eventually scaling up to tens of thousands in commercialization.
“What works on a small, clinical phase is not always practical,
or possibly even necessary at a much larger scale.”
~Adrian Lee-Mohan
That’s why to align clinical and commercial phases, to plan for all scenarios, it’s critical to involve an experienced logistics partner from the beginning. This not only allows for more streamlined, reliable solutions – logistics partners can play a role in educating all those involved in the supply chain – airlines, ground handlers and more.
“If you involve a logistics partner early on, even before the
clinical stage, you can flush any issues out, mitigate risk and
come up with creative ideas on how to approach things.”
~David Murphy
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