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WebApr 11, 2024 · "Fast Track designation, along with our capabilities to conduct our clinical trials using commercial-scale cGMP material, will further support the efficient development of RGX-202 from clinic to commercial readiness," said Kenneth T. Mills, President, and Chief Executive Officer of REGENXBIO. "RGX-202 is a key part of our '5x25' strategy, and ... Web22 hours ago · FDA designation comes as AFFINITY DUCHENNE study is underway. by Marisa Wexler, MS April 13, 2024. The U.S. Food and Drug Administration (FDA) has granted fast track designation to RGX-202, a one-time gene therapy for Duchenne muscular dystrophy (DMD) that is in early clinical trials. The FDA gives this designation … red copper mug 2-pack
SAB Biotherapeutics Granted Fast Track Designation from FDA for …
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