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Form Bio and Cure Rare Disease partnered to accelerate gene therapy for Duchenne muscular dystrophy using AI, boosting manufacturing efficiency from 13% to 59%.
Form Bio and Cure Rare Disease (CRD) have formed a partnership to speed up development of gene therapies for rare neuromuscular diseases, beginning with Duchenne muscular dystrophy (DMD).
Using Form Bio’s AI-powered platform, the teams boosted the proportion of full-length AAV vectors from 13% to 59% in one month, significantly improving manufacturing efficiency and therapy safety.
This advance enables CRD to move its DMD candidate into in vivo preclinical testing with greater confidence.
The collaboration combines nonprofit mission-driven research with AI-driven biotech innovation to reduce development time, cost, and risk, aiming to deliver treatments for patients with few or no options.
Form Bio y Cure Rare Disease se asociaron para acelerar la terapia génica para la distrofia muscular de Duchenne utilizando AI, aumentando la eficiencia de fabricación del 13% al 59%.