REGENXBIO Inc. announced the closing of its previously announced strategic partnership with Nippon Shinyaku. Under the terms of the agreement, REGENXBIO and Nippon Shinyaku will develop and commercialize RGX-121 (clemidsogene lanparvovec) for Mucopolysaccharidosis II (MPS II), also known as Hunter syndrome and RGX-111 for MucopolysaccharIDosis I (MPS I), also known as Hurler syndrome in the United States and Asia. RGX-111 has received Orphan Drug Product, Rare Pediatric Disease and Fast Track designations from the U.S. Food and Drug Administration. REGENXBIO Inc. announced the closing of its previously announced strategic partnership with Nippon Shinyaku. Under the terms of the agreement, REGENXBIO and Nippon Shinyaku will develop and commercialize RGX-121 (clemidsogene lanparvovec) for Mucopolysaccharidosis II (MPS II), also known as Hunter syndrome and RGX-111 for MucopolysaccharIDosis I (MPS I), also known as Hurler syndrome in the United States and Asia. RGX-111 has received Orphan Drug Product, Rare Pediatric Disease and Fast Track designations from the U.S. Food and Drug Administration.
REGENXBIO is a Maryland-based biotechnology company that researches and develops gene therapeutics for the treatment of retinal, metabolic, and neurodegenerative diseases.