食品药品监督管理局
药品审批
靶向治疗
医学
重症监护医学
药品
药理学
内科学
癌症
作者
Maximilian Julve,Mark P. Lythgoe,James R. Larkin,Andrew J.S. Furness
标识
DOI:10.1016/j.trecan.2024.04.003
摘要
The US Food and Drug Administration (FDA) approval of lifileucel, for advanced melanoma, represents the first cellular therapy to reach the clinic for solid cancers. Here, we summarise this landmark approval, consider the associated regulatory pathway, and evaluate the challenges that remain to ensure effective implementation of this advanced 'living' therapy.
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