$SGMO The leader in therapeutic genome editing,
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The leader in therapeutic genome editing, announced today that the Company has received notice from the U.S. Food and Drug Administration ( FDA ) of special regulatory designations for three of the Company's clinical programs.
The FDA has granted orphan drug status for SB-525 cDNA gene therapy for Hemophilia A.
There's also fast track designation for SB-FIX in vivo genome editing treatment for Hemophilia B, and Rare Pediatric Disease designation for SB-913 in vivo genome editing treatment for Mucopolysaccharidosis Type II (MPS II).