CRISPR Therapeutics AG is at the forefront of gene editing, pioneering treatments for serious diseases through its CRISPR/Cas9 technology. This innovative approach allows for precise DNA modifications, offering hope in areas like hemoglobinopathies, immune-oncology, autoimmune diseases, and type 1 diabetes. Its leading therapy, CASGEVY, aims to transform care for patients with severe blood disorders through gene-edited cell therapy. Additionally, the company is developing cutting-edge CAR T cell therapies and in vivo gene editing solutions, working in strategic partnerships to advance its mission of curing complex diseases.