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Mike Patterson, Curium’s North American Chief Executive Officer, said: “As the only vertically integrated, lutetium-based NETs therapy manufacturer, Curium™ is uniquely positioned to support a reliable supply of BEXLUTRY™ and help sites of care prepare for radioligand therapy delivery at scale. Today’s FDA approval brings us a step closer to advancing our ambition of aiming to improve the lives of up to 80% of patients with cancer. Our priority now is a high-quality launch supported by our end-to-end nuclear medicine infrastructure, designed to help ensure consistent delivery, predictable scheduling support for sites of care, and a dependable experience for patients receiving radioligand therapy.”
