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原话 生物医药与基因·

A $2 million CRISPR therapy cannot reach most patients

“这个价格显然无法让大多数本可受益的人用上这种疗法,”她说。

English original

"That is clearly not a price point that will make this available to most people that can benefit from it," she said.

谈及200万美元的镰状细胞CRISPR疗法时

J
珍妮弗·杜德纳Innovative Genomics Institute · 执行董事

报道摘要

CRISPR gene editing, which slices DNA to treat diseases, had its first-ever systemic delivery in a human body. Jennifer Doudna, who won the 2020 Nobel Prize in chemistry for her work on CRISPR, called ...

CNBC

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CRISPR's bottleneck is delivery, not the editors

““这在临床医学中尤其是个问题:能够编辑脑细胞、心脏细胞或肌肉细胞具有巨大潜力,但目前我们并没有把这些编辑工具送入那些细胞的工具,”杜德纳说。“我们有编辑器,只是不知道如何把它们送到需要去的地方。””

生物医药与基因·6月30日·CNBC

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