/PRNewswire/ REGENXBIO Inc. (Nasdaq: RGNX) today announced that the U.S. Food and Drug Administration (FDA) has granted Fast Track designation for RGX-202,.
Regenxbio (RGNX) Presents Additional Positive Interim Data from Phase I/II Trial of RGX-111 for Treatment of Severe MPS I streetinsider.com - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from streetinsider.com Daily Mail and Mail on Sunday newspapers.
RGX-111 is an investigational AAV Therapeutic for the treatment of severe MPS I that is part of REGENXBIO s clinical-stage pipeline of neurodegenerative.