Today, the FDA approved the world’s first ‘gene-editing’ therapy, Casgevy. This treatment for sickle cell disease (SCD) is based on the 2020 Nobel Prize-winning CRISPR/Cas9 technology and is developed by Aescap portfolio companies Crispr and Vertex
Today, the FDA approved the world’s first ‘gene-editing’ therapy, Casgevy. This treatment for sickle cell disease (SCD) is based on the 2020 Nobel Prize-winning CRISPR/Cas9 technology and is developed by Aescap portfolio companies Crispr and Vertex