– Biotech startup Spotlight therapeutics has shut down due to disappointing preclinical results, despite raising $66 million from prominent investors like GV.
– Founded in 2018 by scientists from UC Berkeley and UCSF, the company aimed to develop innovative gene-editing therapies without viral vectors or nanoparticle delivery.
– Casgevy (exagamglogene autotemcel), the frist FDA-approved CRISPR-Cas9-edited therapy for sickle cell disease, faced post-approval layoffs of 10% staff citing economic challenges.
– Intellia Therapeutics also reduced its workforce by a quarter in January 2025 and narrowed its pipeline, ceasing research into α1-antitrypsin deficiency treatment.
The closures and workforce reductions highlight how cutting-edge biotech innovations like CRISPR face critically important hurdles despite scientific advancements. While these technologies offer groundbreaking potential for treating previously “undruggable” diseases, stringent market conditions and inconsistent outcomes underscore the financial risks involved in developing transformative medicines.
For India-home to a rapidly growing biotechnology sector-the situation serves as an critically important lesson for balancing innovation with sustainable funding models and contingency planning during early development stages. As India’s startups increasingly venture into advanced gene-editing projects inspired by global initiatives, these examples encourage cautious optimism over unbridled enthusiasm in pursuing ambitious therapeutic technologies.