NewslettersMuscle Cell NewsPepGen Receives US FDA Orphan Drug and Rare Pediatric Disease Designations for PGN-EDO51 for the Treatment of Duchenne Muscular DystrophyBy Noshin Noorjahan - March 18, 2024034PepGen Inc. announced that the US FDA granted both orphan drug and rare pediatric disease designations for PGN-EDO51, an investigational therapeutic for Duchenne muscular dystrophy.[PepGen Inc.]Press Release