and the European Union is approximately 47,300 patients/year. The estimated incidence of NETs for the combined populations of the U.S. in two forms: as a kit for reconstitution using a Ga 68 generator, and as Netspot Injection, a ready-to-use dose delivered from a local radiopharmacy in selected metropolitan areas. The product will be available in the U.S. Gallium Ga 68 dotatate received Orphan Drug Designation from both the FDA and European Medicines Agency (EMA) in March 2014.įollowing approval, Netspot will be made available to the U.S. It is the first approved drug using Ga 68 as a positron emitter. Netspot is the new market name for Somakit-TATE (a kit for the preparation of gallium Ga 68 dotatate injection) in the U.S. PLEASE confirm coverage with insurer prior to the scan. Medicare does provide coverage for NETSPOT but not all private insurance does. Before you go for your scan confirm how the scan will be paid for. Netspot received approval following a Priority Review from the FDA. As of Jthe FDA approved Ga68 DotaTate Scan (NETSPOT (tm)) for Neuroendocrine Tumors. The FDA has approved Netspot (Somakit-TATE) for the localization of somatostatin receptor positive neuroendocrine tumors (NETs) in adult and pediatric patients. Facing Ethical Challenges with Strength and Compassion.
#Netspot neuroendocrine professional#
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