Proprietary ExoEdit™ gene editing in exosomes for rare neurodegenerative diseases
Deliver CRISPR/Cas gene editing to brain cells in patients with rare neurodegenerative diseases; Target and knock-down disease-causing genes in central nervous system; Develop therapies for conditions like ALS and Parkinson's disease; Advance clinical translation of exosome-based gene therapies; Conduct preclinical studies in animal models of neurodegeneration
Named in Nature Biomedical Engineering publication; Co-founded by Professor Matthew Wood and Dr. Per Lundin; Backed by Oxford Sciences Innovation; Developed ExoEdit™ technology from Oxford and Karolinska Institutet research; Pipeline includes therapies for ALS and Parkinson's disease