For 21-year-old Javarian Weatherspoon, life without pain feels like a miracle. After growing up with sickle cell disease, he ...

Editas Medicine reports successful gene editing levels in stem cells, supporting potential treatment for sickle cell disease and beta thalassemia. Editas Medicine announced promising new data on ...

While the medical world is melting down from the absolute apocalypse that is RFK Jr., it's good to celebrate that (at least ...

The one-off treatment highlights the promise of a new type of gene editing and the challenges of using it to treat extremely ...

The personalized CRISPR treatment could be the future of gene therapy, but hurdles remain before everyone has access.

“This is the first step towards the use of gene editing therapies to treat a wide variety of rare genetic disorders for which ...

A team of doctors at the Children's Hospital of Philadelphia and Penn Medicine treated a baby with a gene editing technology ...

A team of researchers at Columbia, Harvard and University of Minnesota has developed a gene editing technique they say could ...

It’s a non-viral, ex vivo gene-editing therapy to correct the genetic mutation responsible for sickle cell disease [SCD] and beta-thalassemia [TDT]. Moreover, Casgevy requires collecting the ...

A CRISPR treatment seems to have been effective for a baby’s devastating disease, but it is not clear whether such bespoke ...