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A team of doctors at the Children's Hospital of Philadelphia and Penn Medicine treated a baby with a gene editing technology customized for his rare disease for the first time ever.

The Center for Pediatric CRISPR Cures will start by creating custom therapies for eight patients with rare immune or metabolic genetic diseases.

World’s first personalized CRISPR therapy given to baby with genetic disease Prime Medicine, a biotechnology company in Cambridge, Massachusetts, unveiled the results on 19 May.

Two Chinese biotechs are testing CRISPR gene editing in boys with muscular dystrophy, even as projects at U.S. companies like Vertex have slowed.