Production of radiometal-based radiopharmaceuticals at a clinical scale via droplet-scale radiochemistry

NIH RePORTER · NIH · R41 · $275,773 · view on reporter.nih.gov ↗

Abstract

PROJECT SUMMARY Despite the enormous value of radiopharmaceuticals for imaging and therapy in clinical nuclear medicine, and for research and drug development, the production of these compounds remains very expensive because of the need for complex, capital-intensive equipment and infrastructure (i.e., hot cells, stack monitor, radiosynthesizer, and a suite of QC testing equipment) at each site. For the most widely used PET radiopharmaceutical, [18F]FDG, multiple patients can be scheduled on the same day, enabling the batch production costs to be divided among many individual doses. However, for most other PET tracers, such cost-sharing opportunities are rare or non-existent, meaning that each production run is effectively dedicated to a single patient, resulting in a high cost per patient dose. These challenges discourage manufacturers from investing in the production of valuable but less-used radiopharmaceuticals, which severely limits their availability. Additionally, the high price of many radiopharmaceuticals discourages their use in research (e.g. pre-clinical), and hampers the development and validation of novel radiopharmaceuticals. In addition to limited demand, some radiopharmaceuticals are constrained by supply-side issues (e.g. limited output of Ga-68 generators) that inherently limits the number of patient doses that can be made in a single batch. Instead of relying on cost reductions through increased demand for radiopharmaceuticals and increase size of batches produced, which will be impossible for many cases, our strategy is to lower the batch production cost itself. New microfluidic methods of PET tracer manufacture have emerged in recent years with the potential to revolutionize tracer production via dramatic reductions in cost and complexity. The droplet-based approach developed by the van Dam laboratory at UCLA enables the production of numerous 18F-radiopharmaceuticals with ~100x reagent reduction, 2-3x reduction in synthesis and purification time, and high molar activity, all in a system the size of a coffee cup. Droplet reactions were scaled to clinically-relevant amounts (one to many patient doses) by using an upstream radioisotope concentrator. DropletPharm, Inc. is commercializing a benchtop radiopharmacy platform based on this technology that will enable a transformation to low-cost production of a broad range of radiopharmaceuticals. Though most of the prior development of droplet radiochemistry has focused on 18F-radiopharmaceuticals, there is intense interest in radiometal isotopes for imaging and therapy, with a large number of Ga-68 compounds in pre-clinical development, clinical trials and a few with FDA-approval for routine use. In this Phase I STTR project, we aim to expand the applications of DropletPharm’s droplet radiochemistry approach beyond F-18 radiotracers by building a metal-free droplet reactor and establishing the feasibility of radiometal labeling. We will develop radioisotope concentration methods f...

Key facts

NIH application ID
10697509
Project number
1R41EB034168-01A1
Recipient
DROPLETPHARM INC.
Principal Investigator
Jason Jones
Activity code
R41
Funding institute
NIH
Fiscal year
2023
Award amount
$275,773
Award type
1
Project period
2023-09-01 → 2026-08-31