Comment on FDA Approves World’s First Crispr Gene-Editing Drug for Sickle-Cell Disease | Landmark decision heralds a new type of medicine that can tackle genetic conditions that are hard to treat

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silence7@slrpnk.net ⁨1⁩ ⁨year⁩ ago

The pricing is higher than you’re describing - about 2 million dollars, which is still cheaper than paying for ongiong treatment over the course of a person’s life.

It’s priced to be attractive to corporate-sponsored insurance plans, not for individuals to pay out of pocket.

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