Epic Bio Presents Preclinical Data on EPI-321 for Facioscapulohumeral Muscular Dystrophy at ASGCT 26th Annual Meeting
Oral presentation highlights EPI-321 effects on multiple clinically relevant markers –
Excerpt from the Press Release:
– Epic Bio, a biotechnology company developing therapies to modulate gene expression using compact, non-cutting dCas proteins, today presented promising preclinical data supporting development of EPI-321 for the treatment of facioscapulohumeral muscular dystrophy (FSHD). The data were shared in an oral presentation at the 26th Annual Meeting of the American Society of Gene & Cell Therapy (ASGCT) taking place May 16-20, 2023, in Los Angeles, Calif.
“We’re proud to share the preclinical data from our lead program, EPI-321, in an oral presentation at the distinguished ASGCT meeting,” said Alexandra Collin de l’Hortet, Ph.D., head of therapeutics at Epic Bio. “We chose FSHD as our lead indication in recognition of the serious unmet need for a therapy that could address the underlying epigenetic cause of the disease. EPI-321’s observed effects on multiple clinically relevant disease measures provide promising direction as we work to translate these findings into the clinic.”
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