Tempus获FDA批准肿瘤专用Xt Cdx，实现其整个DNA实体瘤产品组合的迁移

美股速递05-29 20:15

Tempus AI宣布，其肿瘤专用Xt伴随诊断产品已获得美国食品药品监督管理局的批准。这一关键监管里程碑使得该公司能够将其整个基于DNA的实体瘤产品组合迁移至这一新获批的平台。

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