November 30, 2020 -- Spotlight Therapeutics has closed $30 million in series A financing to advance its nonviral gene editing therapeutics for in vivo editing.
Spotlight's proprietary targeted active gene editor (TAGE) technology platform develops programmable CRISPR ribonucleoproteins optimized for in vivo cell-targeted delivery. The company's approach avoids complexities and toxicities associated with cell, viral, and nanoparticle-based delivery methods. Lead candidates include those targeting hemoglobinopathies and immune-oncology applications.
The series A financing was led by GV, formerly Google Ventures.