CRISPR Therapeutics Provides Business Update and Reports Second Quarter ...
π CRISPR Therapeutics reported Q2 2026 financial results and provided a business update on August 3, 2026.
β CASGEVY momentum continues with FDA approval extended to children as young as 2 years old for sickle cell disease and transfusion-dependent beta thalassemia.
𧬠Phase 1 clinical trials were initiated for CTX340 (refractory hypertension) and CTX460 (alpha-1 antitrypsin deficiency).
π€ Vertex Pharmaceuticals leads global development and commercialization of CASGEVY under a 60/40 profit-sharing agreement.
π CRISPR Therapeutics is advancing in vivo liver editing programs using its proprietary SyNTase technology for cardiovascular indications.
𧬠Zugocabtagene geleucel (zugo-cel) advances as an allogeneic CAR T cell therapy for autoimmune diseases and oncology.
π©Έ Collaboration with Sirius Therapeutics develops CTX611, a long-acting siRNA targeting coagulation factor XI.
- CASGEVY demonstrates strong market momentum with regulatory expansion to include pediatric patients as young as two years old.
- The company successfully initiated Phase 1 clinical trials for two new in vivo programs, CTX340 and CTX460, expanding its therapeutic reach.
- Strategic collaborations with Vertex and Sirius Therapeutics provide a diversified pipeline spanning gene editing and siRNA technologies.