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Researchers, For The First Time, Injected CRISPR Drug Into The Blood Of People Afflicted With Transthyretin Amyloidosis—A Rare Deadly Liver Disease. And Early Results Show That, In 3 Persons, The CRISPR Drug Alleviated Toxic Protein Production Close To The Liver, Indicating Possible Success For Injectable CRISPR Treatment.

CRISPR Gene-Editing Breakthrough Opens Door To Treating Broad Array Of Diseases : Shots – Health News : NPR

https://www.npr.org/sections/health-shots/2021/06/26/1009817539/he-inherited-a-devastating-disease-a-crispr-gene-editing-breakthrough-stopped-it

Scientists successfully treated a rare disease with the experimental gene-editing technique. It could open the door to new ways of treating more common disorders in the future.