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Oct 18: The gene therapy space celebrated another first on Wednesday, as the FDA cleared the way for the first-ever investigational in vivo CRISPR-based gene editing therapy to enter late-stage development

*Correspondence: Xiao-Yu Li, [email protected] This article was submitted to Cancer Immunity and Immunotherapy, a section of the journal Frontiers in Oncology Disclaimer All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers

TABLE 3 Innovative molecular pathways of nanoparticles for cancer treatment

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