Victoria Gray is the first person in the world to receive CRISPR,  a gene-editing therapy for sickle cell disease created by ...

KJ Muldoon, a 10-month-old baby, was diagnosed with the genetic disease carbamoyl-phosphate synthetase 1 deficiency after he ...

Leaders from the world of cell and gene therapy shared their personal stories and policy recommendations in an extraordinary roundtable conducted by the FDA in front of its recently-appointed top ...

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

In medical breakthrough, a baby diagnosed with rare genetic disorder is thriving after customized CRISPR gene editing therapy ...

KJ Muldoon came into the world with a genetic time bomb ticking inside him.

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

Innovations in gene editing, expanding global diagnostic infrastructure, and strong government initiatives are driving the hemoglobinopathies market's projected 11.56% CAGR through 2032, according to ...