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FDA Approves Bexlutry (lutetium Lu 177 dotatate) for the Treatment of Somatostatin Receptor-Positive Gastroenteropancreatic Neuroendocrine Tumors in Adults

October 7, 2026

Boston, MA – 14 September, 2026 – Curium™ announced today that the U.S. Food and Drug Administration (FDA) has approved its New Drug Application (NDA) for Bexlutry™ lutetium Lu 177 dotatate injection for the treatment of…

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FDA Acceptance

Adults, Bexlutry, FDA Approval, lutetium Lu 177 dotatate, Somatostatin Receptor-Positive Gastroenteropancreatic Neuroendocrine Tumors

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