Lantheus宣布FDA批准Tauklarify™(氟喹他F18注射液)——阿尔茨海默病F18标记tau蛋白PET成像试剂

美股速递
Aug 14

Lantheus Holdings, Inc.(简称Lantheus)近日宣布,美国食品药品监督管理局(FDA)已正式批准其新药Tauklarify™(Florquinitau F 18 Injection,即氟喹他F18注射液)。该药物是一种采用F18标记的tau蛋白正电子发射断层扫描(PET)成像试剂,专门用于阿尔茨海默病的诊断与评估。

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