Session 2 of Bracken's Radiopharma Roundtable paired a teaching talk from Ben Larimer with an open panel: Anna Pokorska-Bocci and Deepak Behera working through the strategic calls that decide whether an early radiopharmaceutical program succeeds, long before the isotope's clock starts ticking. Recorded September 16, 2026.
Ben’s argument is to skip the therapeutic vs. theranostic framing and ask why you’d want a diagnostic at all. A good targeting molecule can enter a Phase 0 or Phase 1 imaging study on a lighter regulatory footing, and you learn whether it engages the target before any therapeutic dose goes in.
Activity, mass, schedule, cycles. Deepak’s view is that dosimetry too often gets run as a retrospective analysis. Build it into the design using imaging, and Phase 2 and Phase 3 start from better dose rationale, where failure is most expensive.
DOTA is familiar and royalty-free, which is why it becomes the default. The panel argued for matching the imaging isotope to the therapeutic isotope’s chemistry first, even if that means a different chelator. The choice also decides your supply model, centralized or site by site.
Sites need radiochemistry, scanner access and dosimetry expertise, and all of it has to produce reproducible measurements. Vendor splits mirror that: physical supply on one side, CRO and data management on the other. Anna’s fix is a single CRO spanning imaging, dosimetry and clinical operations.
"The half-life is the easy part. It's fixed physics. The hard part is everything you have to do before the half-life clock even starts ticking."
"It's not simply how many sites are open, but how reliably can we treat patients safely and obtain the complete data that we need for the next decision."
"It's an important thing to discuss before you see the images, because then a decision has to be made."
New panel, same format. Time and topic to come.
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